家族性多发性脂肪瘤病1例报告及诊断方法并复习文献

Kartavya Kumar Verma
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引用次数: 0

摘要

脂肪瘤是一种众所周知且最常见的软组织肿瘤。但多发性脂肪瘤病是罕见的。此外,还记录了综合征相关性。家族性多发性脂肪瘤病是一种常染色体显性遗传病。它表现为体内特定部位的多个脂肪瘤。在本病例中,26岁的患者自诉前臂、大腿和前腹壁多发肿胀5年。多发性脂肪瘤病的诊断是由细针吸细胞学和组织病理学检查证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case report of familial multiple lipomatosis and its diagnostic approach with review of literatures
Lipoma is a well-known and most common soft tissue tumor. But multiple lipomatosis are rare. Also, syndromic associations were documented. Familial multiple lipomatosis (FML) is an autosomal dominant disorder. It presents as multiple lipomas in the body at specific sites. In presenting case 26-year-old patient complained of multiple swellings in his forearms, both thigh, and anterior abdominal wall for 5 years. A diagnosis of multiple lipomatosis is made by Fine needle aspiration cytology and confirmed by histopathological examination.
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