Case Report
DOI:
DOI: http://dx.doi.org/10.24327/ijrsr.20231412.0823
Subject:
Medical
KeyWords:
Malignant mixed germ cell tumor, Dysgerminoma, Yolk sac tumor, immature teratoma, Embryonal carcinoma.
Abstract:
Malignant ovarian germ cell tumors (MOGCTs) are rare but predominantly affect young women and adolescent girls. They typically present with pelvic masses or abdominal pain. Histologically, they are divided into dysgerminomas and non-dysgerminomatous tumors. This report presents a case of malignant mixed germ cell tumor diagnosed initially through ultrasound, CT, and MRI evaluations, later confirmed via biopsy.