Liver metastasis from an ovarian Yolk-Sac-Tumor: A case report and review of the literature

E. Fatima, M. Michouar, A. A. Errami, S. Oubaha, Z. Samlani, K. Krati
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Abstract

The endodermal sinus tumor or Yolk sac tumor is a rare ovarian tumor that classically occurs in adolescents and young women, it is a histological type rarely found in clinical practice. We report the case of a 24-year-old woman presenting with an ovarian tumor of the endodermal sinus with hepatic metastasis revealed by a painful abdominal mass in the right hypochondrium associated with a deterioration of the general condition. The blood Alpha-Fetoprotein (AFP) level was 71,300 ng / ml. Abdominal magnetic resonance imaging revealed multiple liver nodules and masses, associated with a magma of secondary lymphadenopathy. The immunohistological study of the hepatic puncture biopsy allowed the diagnosis of a hepatic localization of an ovarian endodermal sinus tumor (Yolk-Sac-Tumor). The tumor was classified stage IV-B of the FIGO 2014 classification, which does not allow a curative approach. Chemotherapy treatment (BEP protocol) was started.
卵巢卵黄囊肿瘤肝转移一例报告及文献复习
卵巢内胚乳窦瘤或卵黄囊瘤是一种罕见的卵巢肿瘤,多发生于青少年和年轻女性,是临床上罕见的组织学类型。我们报告的情况下,24岁的妇女提出卵巢肿瘤的内皮窦肝转移显示一个痛苦的腹部肿块在右胁肋,并伴有一般情况的恶化。血甲胎蛋白(AFP)水平为71300 ng / ml,腹部磁共振成像显示多发肝结节和肿块,伴有继发性淋巴结病变。肝脏穿刺活检的免疫组织学研究允许肝脏定位卵巢内胚层窦瘤(卵黄-囊腺-肿瘤)的诊断。根据FIGO 2014的分类,该肿瘤被划分为IV-B期,这并不允许治疗方法。开始化疗(BEP方案)。
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