Poudel Aashish, Sedain Prajwal, Pokhrel Biraj, Sapkota Aakash, Chamlagain Anita, Sharma Nisha, Rajbhandary Sanyukta, Khaniya Bishal, Ojha Neebha
Department of Gynecology and Obstetrics Tribhuwan University Teaching Hospital, Institute of Medicine Kathmandu Nepal.
Department of Pathology Tribhuwan University Teaching Hospital, Institute of Medicine Kathmandu Nepal.
Clin Case Rep. 2023 Dec 19;11(12):e8335. doi: 10.1002/ccr3.8335. eCollection 2023 Dec.
Yolk sac tumors are rare and malignant germ cell tumors of the ovary occurring in children and young women. Fertility-sparing surgical intervention with adjuvant chemotherapy has shown to improve prognosis.
We present a case of a 14-year-old girl who presented with the complaints of lower abdominal pain and distention. Her tumor markers were increased, and radiological investigation suggested the diagnosis of malignant left ovarian mass. Histopathology confirmed the diagnosis of Yolk sac tumor. She was subsequently managed with fertility-sparing surgery and adjuvant chemotherapy.
卵黄囊瘤是发生于儿童和年轻女性卵巢的罕见恶性生殖细胞肿瘤。保留生育功能的手术干预联合辅助化疗已显示可改善预后。
我们报告一例14岁女孩,她因下腹部疼痛和腹胀就诊。其肿瘤标志物升高,影像学检查提示左侧卵巢恶性肿块。组织病理学确诊为卵黄囊瘤。随后她接受了保留生育功能的手术和辅助化疗。