Sinaa Mohamed
Service d'Anatomie et de Cytologie Pathologique, Hôpital militaire Moulay Ismail, Meknès, Morocco.
Pan Afr Med J. 2016 Dec 21;25:254. doi: 10.11604/pamj.2016.25.254.10398. eCollection 2016.
Liposarcoma is an extremely rare malignant adipose mesenchymal tumor. World Health Organization classifies liposarcomas into five subtypes: well differentiated, myxoid, pleomorphic, dedifferentiated and mixed. The association between multiple and synchronous location of several subtypes of liposarcomas is exceptional. Only 34 cases have been reported in the literature. We report the case of synchronous association between retroperitoneal dedifferentiated liposarcoma and two small well-differentiated lipoma-like pericolic liposarcomas. Anatomopathological aspects, therapeutic options and prognostic factors of liposarcomas have been reviewed in this study.
脂肪肉瘤是一种极其罕见的恶性脂肪间叶组织肿瘤。世界卫生组织将脂肪肉瘤分为五个亚型:高分化型、黏液型、多形性、去分化型和混合型。脂肪肉瘤的几种亚型出现多处同时发生的情况极为罕见。文献中仅报道过34例。我们报告一例腹膜后去分化脂肪肉瘤与两个小的高分化脂肪瘤样结肠旁脂肪肉瘤同时发生的病例。本研究对脂肪肉瘤的解剖病理学特征、治疗选择和预后因素进行了综述。