[畸形腹膜后脂肪肉瘤1例报告]。

M. Niedergethmann, R. Hildenbrand, M. Winkler
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引用次数: 2

摘要

脂肪肉瘤约占软组织肉瘤的20%,发生在腹膜后间隙的占14%,起源于肾周脂肪的三分之一。我们报告了一例巨大的、可切除的、分化良好的腹膜后脂肪肉瘤。主要症状为腹痛、腹胀和体重增加。磁共振成像显示一个巨大的腹膜后肿瘤疑似高分化脂肪肉瘤。可获得肿瘤的根治性切除。只有50%的肿瘤被切除而无残留肿瘤,10年后90%的肿瘤复发是主要的治疗挑战。由于新辅助和辅助治疗以及术中放疗未能证明预后价值,因此治疗性切除仍然是原发性和复发性脂肪肉瘤的主要治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Monstrous, retroperitoneal liposarcoma--a case report].
Liposarcomas comprise about 20% of soft tissue sarcomas and occur in 14% in the retroperitoneal space originating in one third from the perirenal fat. The case of a patient with an extraordinary huge, resectable, well-differentiated retroperitoneal liposarcoma is reported. The presenting symptoms were abdominal pain and distension as well as weight gain. Magneticresonance imaging revealed a huge retroperitoneal tumor suspected of well-differentiated liposarcoma. Curative resection of the tumor could be obtained. Only 50% of all tumors are excised without residual tumor and recurrence, occurring in 90% after 10 years, is the main therapeutic challenge. Since neoadjuvant and adjuvant therapy as well as intraoperative radiotherapy failed to prove prognostic value, curative resection remains the main treatment for primary and recurrent liposarcomas.
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