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703599008: Microcystic stromal tumor (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3009233019 Microcystic stromal tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009646016 Microcystic stromal tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009667016 Microcystic stromal tumor (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009233019 Microcystic stromal tumor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009233019 Microcystic stromal tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009646016 Microcystic stromal tumour en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009646016 Microcystic stromal tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009667016 Microcystic stromal tumor (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009667016 Microcystic stromal tumor (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microcystic stromal tumor (morphologic abnormality) Is a Sex cord-stromal tumour, benign true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
A rare benign ovarian stromal tumor characterized by a stromal neoplasm with variable microcystic morphology, low mitotic activity, and diffuse nuclear beta-catenin and cyclin D1 immunoreactivity, while inhibin and calretinin are not expressed. Patients 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 True Microcystic stromal tumor (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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