1187463001: Microcystic stromal tumor of ovary (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\...

\Pelvic organ finding (finding)\Ovary finding\...

\Mass of ovary\Neoplasm of ovary\...

\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Disease of ovary\Lesion of ovary\Neoplasm of ovary\...

\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic organ finding (finding)\Ovary finding\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic organ finding (finding)\Ovary finding\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic organ finding (finding)\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic organ finding (finding)\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Finding of pelvis\Pelvic mass\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Ovary finding\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Ovary finding\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of pelvic region of trunk (finding)\Female genitalia finding\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Pelvic organ finding (finding)\Ovary finding\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Pelvic organ finding (finding)\Ovary finding\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Pelvic organ finding (finding)\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Pelvic organ finding (finding)\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Mass of female genital structure (finding)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Ovary finding\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Ovary finding\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Genital finding\Female genitalia finding\Ovary finding\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Finding of trunk structure\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Mass of female genital structure (finding)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Mass of urogenital structure\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Mass of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Mass of uterine adnexa (finding)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Pelvic mass\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Neoplasm of endocrine system (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of pelvis (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of pelvic region of trunk (disorder)\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Lesion of genitalia (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital system\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of female reproductive system (disorder)\Disorder of female genital organs (disorder)\Disease of ovary\Lesion of ovary\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of abdomen (disorder)\Neoplasm of intra-abdominal organs\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of female genital organ\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Sex cord tumor of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Neoplasm of ovary\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Neoplasm of uterine adnexa (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Neoplasm of pelvis (disorder)\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign genital neoplasm\Benign neoplasm of female genital organ\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of abdomen (disorder)\Benign neoplasm of intra-abdominal organs\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.
\Disease\Disorder of trunk (disorder)\Neoplasm of trunk (disorder)\Benign neoplasm of trunk\Benign neoplasm of pelvis\Benign neoplasm of uterine adnexa\Benign neoplasm of ovary\Benign sex cord tumour of ovary\A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4673868011 Microcystic stromal tumour of ovary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673869015 Microcystic stromal tumor of ovary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673870019 Microcystic stromal tumor of ovary (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673871015 MCST (microcystic stromal tumor) of ovary en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

4673872010 MCST (microcystic stromal tumour) of ovary en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5399618017 A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5399619013 A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4673868011 Microcystic stromal tumour of ovary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673869015 Microcystic stromal tumor of ovary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673870019 Microcystic stromal tumor of ovary (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4673871015 MCST (microcystic stromal tumor) of ovary en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

4673872010 MCST (microcystic stromal tumour) of ovary en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

4673862012 A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4673863019 A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5399618017 A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5399619013 A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3387801001000114 Mikrozystischer Stromatumor de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3387801001000114 Mikrozystischer Stromatumor de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	Is a	Benign sex cord tumour of ovary	true	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	Finding site	Ovarian structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	Associated morphology	Microcystic stromal tumor (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4673868011	Microcystic stromal tumour of ovary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673869015	Microcystic stromal tumor of ovary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673870019	Microcystic stromal tumor of ovary (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673871015	MCST (microcystic stromal tumor) of ovary	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4673872010	MCST (microcystic stromal tumour) of ovary	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399618017	A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399619013	A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4673868011	Microcystic stromal tumour of ovary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673869015	Microcystic stromal tumor of ovary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673870019	Microcystic stromal tumor of ovary (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4673871015	MCST (microcystic stromal tumor) of ovary	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4673872010	MCST (microcystic stromal tumour) of ovary	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4673862012	A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4673863019	A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399618017	A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumor may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399619013	A rare benign ovarian stromal tumour characterised by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients most commonly present with symptoms of a unilateral pelvic mass. Hormonal manifestations are usually absent. The tumour may be associated with familial adenomatous polyposis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3387801001000114	Mikrozystischer Stromatumor	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3387801001000114	Mikrozystischer Stromatumor	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module