FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

123631000119103: Malignant poorly differentiated neuroendocrine carcinoma (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3288879013 Malignant poorly differentiated neuroendocrine carcinoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3288919019 Malignant poorly differentiated neuroendocrine carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6378581000241112 carcinome neuroendocrine malin peu différencié fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    carcinome neuroendocrine malin peu différencié Is a Neuroendocrine carcinoma false Inferred relationship Some
    carcinome neuroendocrine malin peu différencié Associated morphology Neuroendocrine tumor false Inferred relationship Some 1
    carcinome neuroendocrine malin peu différencié Associated morphology Neuroendocrine carcinoma, grade 3 false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    carcinome neuroendocrine peu différencié du thymus Is a False carcinome neuroendocrine malin peu différencié Inferred relationship Some
    High-grade neuroendocrine carcinoma of the corpus uteri is an extremely rare, aggressive, primary uterine neoplasm, originating from neuroendocrine cells scattered within the endometrium, characterized, macroscopically, by a bulky, frequently polypoid, mass with abundant necrosis located in the uterus and, histologically, by rosette-like and cord-like structures consisting of small, rounded cells with oval nuclei and scarce cytoplasm. Patients often present with dysfunctional uterine bleeding, pelvic or abdominal mass and, especially in later stages of the disease, abdominal pain. Symptomatic metastatic spread or symptoms related to a paraneoplastic syndrome, such as retinopathy, or Cushing syndrome due to ectopic ACTH production, may be associated. Is a False carcinome neuroendocrine malin peu différencié Inferred relationship Some
    High-grade neuroendocrine carcinoma of the cervix uteri is a rare, aggressive, primary cervical neoplasm, originating from neuroendocrine cells present in the lining epithelium of the cervix, characterized, macroscopically, by usually large lesions, sometimes with a barrel-shaped appearance. Patients often present with abnormal vaginal bleeding or discharge, pelvic/abdominal pain, post-coital spotting and/or dysuria, while symptoms related to carcinoid syndrome are not frequent. Is a False carcinome neuroendocrine malin peu différencié Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start