Magri K, Riethmuller D, Maillet R
Service de Gynécologie Obstétrique, CHU de Besançon, 3, boulevard Alexandre-Fleming, 25000 Besançon.
J Gynecol Obstet Biol Reprod (Paris). 2006 May;35(3):280-2. doi: 10.1016/s0368-2315(06)78314-4.
Primary malignant lymphoma of the ovary is a rare tumor (1,5% of ovarian tumors). Clinically, it occurs as an abdominal mass with pain which can be confused with an epithelial ovary tumor. Most tumors are observed during the fourth decade. Burkitt lymphoma, is sporadic in western countries, usually with abdominal involvement. Diagnosis is guided by biological analysis and imaging. Prognosis depends on medullary and neuromeningeal involvement. Polychemotherapy is required. We report a case of a young woman who developed abdominal Burkitt Lymphoma mimicking advanced-stage bilateral ovarian cancer.
原发性卵巢恶性淋巴瘤是一种罕见肿瘤(占卵巢肿瘤的1.5%)。临床上,它表现为伴有疼痛的腹部肿块,可能会与上皮性卵巢肿瘤相混淆。大多数肿瘤在40岁左右被发现。伯基特淋巴瘤在西方国家为散发性,通常累及腹部。诊断依靠生物学分析和影像学检查。预后取决于髓质和神经脑膜受累情况。需要进行多药化疗。我们报告一例年轻女性病例,其发生的腹部伯基特淋巴瘤酷似晚期双侧卵巢癌。