Endometrioid carcinoma of ovaryGo to external page http://www.orpha.net/ORDO/Orphanet_454723
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.
- has_age_of_onset some eldery
- has_inheritance some not genetically inherited
- has_annual_incidence_range some 1-9 / 1 000 000 and present_in some Europe and has_annual_incidence_average_value value 0.81
- part_of some Malignant epithelial tumor of ovary
- has_age_of_onset some adult
- has_annual_incidence_range some 1-9 / 1 000 000 and present_in some Korea, Republic of and has_annual_incidence_average_value value 0.51