塞内加尔凯杜古阿马特丹索科地区医院的一例腹膜和空肠定位的卵巢幼颗粒细胞瘤病例

Mouhamadou Wade, Thierno A. T. Diallo, Foulaké Tandian, Nankouma Konate, Abdoulaye Keita, Alfred N. Sarr, Ousmane Diop, Doudou Sane, Khadim Faye
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引用次数: 0

摘要

颗粒细胞瘤是一种罕见的卵巢肿瘤,属于性索和基质肿瘤家族。它们是恶性基质肿瘤中最常见的类型,预后良好。卵巢颗粒细胞瘤分为两种类型:成人型(AGCTs)和幼年型(JGCTs),前者最常发生在 40 岁至 70 岁之间,后者并不常见。幼年型颗粒细胞瘤多累及单侧卵巢,主要发生在 30 岁以下的人群中。转移性扩散非常罕见,即使出现转移,也通常局限于腹腔。我们报告了本院接诊的一例卵巢幼年颗粒细胞瘤扩展至空肠和腹膜的 18 岁女性患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of ovarian juvenile granulosa cells tumor with peritoneal and jejunal localisation at Amath Dansokho Regional Hospital, Kedougou, Senegal
Granulosa tumors are rare ovarian tumors they belong to sex-cord and stromal tumor family. They are the most common type of malignant stromal tumor and have a good prognosis. There are two types: the adult type (AGCTs), which occurs most frequently between the ages of 40 and 70, and the juvenile type (JGCTs), which is uncommon. Juvenile granulosa tumors tend to involve a single ovary and occur mainly in people who are younger than 30 years. Metastatic spread is rare and, if present, is usually limited to the peritoneal cavity. We report a case of ovarian juvenile granulosa cell tumor extending to the jejunum and peritoneum in an 18-year-old female patient received in our institution.
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