A rare malignant epithelial tumor of ovary characterized by confluent or cribriform proliferations of round, oval, or tubular glands, typically lined by stratified non-mucin-containing epithelium with well-defined luminal margins. Squamous differentiation, secretory changes, oxyphilic variants, sex cord-stromal type patterns, or sertoliform endometrioid carcinomas may occur. Patients most commonly present in the sixth decade of life, either with a pelvic mass with or without pain, or without any symptoms. The tumor may be bilateral and is frequently associated with endometriosis and/or endometrial carcinoma.

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0346163 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:C56 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=454723
hasDbXref
  • ICD-10:C56
  • UMLS:C0346163
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409949
  • http://www.orpha.net/ORDO/Orphanet_409948
has annual incidence range
  • http://www.orpha.net/ORDO/Orphanet_409976
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409941
notation
  • ORPHA:454723
part of
  • http://www.orpha.net/ORDO/Orphanet_398934
present in
  • http://www.orpha.net/ORDO/Orphanet_410109
  • http://www.orpha.net/ORDO/Orphanet_409984

Term relations

Subclass of: