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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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Malignant poorly differentiated neuroendocrine carcinoma Is a Neuroendocrine carcinoma (disorder) false Inferred relationship Some
    Malignant poorly differentiated neuroendocrine carcinoma Associated morphology neuroendokrint karcinom false Inferred relationship Some 1
    Malignant poorly differentiated neuroendocrine carcinoma Associated morphology neuroendokrint karcinom, grad 3 false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Poorly-differentiated neuroendocrine carcinoma of thymus Is a False Malignant poorly differentiated neuroendocrine carcinoma Inferred relationship Some
    An extremely rare aggressive primary uterine neoplasm, originating from neuroendocrine cells scattered within the endometrium. Macroscopic characteristics are a bulky frequently polypoid mass with abundant necrosis located in the uterus. Histological characteristics are 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 abdominal pain, especially in later stages of the disease. 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 Malignant poorly differentiated neuroendocrine carcinoma Inferred relationship Some
    A rare aggressive primary cervical neoplasm originating from neuroendocrine cells present in the lining epithelium of the cervix. Macroscopic characteristics are 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 Malignant poorly differentiated neuroendocrine carcinoma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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