Frick R, Rummel H, Wurster K, Kaufmann M
Geburtshilfe Frauenheilkd. 1976 Nov;36(11):946-50.
The yolk-sac tumor or endodermal sinus tumor is a rare but highly malignant ovarian teratoma with its highest incidence in young women. The tumor is relatively resistant to radiotherapy but sensitive to combined chemotherapy and should therefore be differentiated in the diagnosis from embryonal carcinoma and radio-sensitive dysgerminomas of the ovary. It is possible that the determination of alpha-fetoprotein is of differential diagnostic value. Two patients are alive and well 8 months and 2 1/2 years following removal of a yolk-sac tumor and primary chemotherapy. One patient received chemotherapy for peritoneal recurrence after removal of the tumor and radiotherapy. She died 1 1/2 years following the primary operation. Long term chemotherapy of the yolk-sac tumor is indicated following operation, irrespective of the stage of the tumor.
卵黄囊瘤或内胚窦瘤是一种罕见但高度恶性的卵巢畸胎瘤,在年轻女性中发病率最高。该肿瘤对放疗相对耐药,但对联合化疗敏感,因此在诊断中应与卵巢胚胎癌和放疗敏感的无性细胞瘤相鉴别。测定甲胎蛋白可能具有鉴别诊断价值。两名患者在切除卵黄囊瘤并进行初次化疗后8个月和2年半仍存活且状况良好。一名患者在肿瘤切除及放疗后因腹膜复发接受化疗。她在初次手术后1年半死亡。无论肿瘤处于何阶段,手术后均需对卵黄囊瘤进行长期化疗。