Testicular Sclerosing Sertoli Cell Tumor

Preferred Label : Testicular Sclerosing Sertoli Cell Tumor;

NCIt definition : A rare testicular Sertoli cell tumor characterized by the presence of neoplastic tubules that are surrounded by a dense fibrotic stroma.;

Neoplastic status : Benign;

Détails

Origin ID

C39945;

UMLS CUI

C1515291;

Disease excludes abnormal cell
- Adenocarcinoma Cell with Intracytoplasmic Mucin [NCIt concept]
- Malignant Cell [NCIt concept]
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Germ Cell [NCIt concept]
- Neoplastic Granulosa Cell [NCIt concept]
- Serous Adenocarcinoma Cell [NCIt concept]
Disease may have findings
- Painless Testicular Mass [NCIt concept]
Has associated anatomic sites
- Genitourinary System [NCIt concept]
- Male Reproductive System [NCIt concept]
- Reproductive System [NCIt concept]
- Testis [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
- Metastatic Lesion [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Sertoli Cell [NCIt concept]
- Neoplastic Sex Cord-Stromal Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Desmoplastic Stroma Formation [NCIt concept]
- Tubular Structures Present [NCIt concept]
disease_has_normal_cell_origin
- Sertoli Cell [NCIt concept]
disease_has_normal_tissue_origin
- Testicular Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Male Reproductive System [NCIt concept]
- Reproductive System [NCIt concept]
- Testis [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome X [NCIt concept]
- Loss of Chromosome 19 [NCIt concept]
- Loss of Chromosome 2 [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]

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