Primary lung liposarcoma
Primary lung liposarcoma
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DOI：
10.1016/s0169-5002(97)00030-5
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发表时间：
1997-07-01
期刊：
影响因子：
5.3
通讯作者：
Vazquez, T
中科院分区：
文献类型：
--
作者：
Krygier, G;Amado, A;Vazquez, T
肺脂肪肉瘤是一种少见的恶性肿瘤，以往仅报道11例。本文报告一例49岁男性局部晚期肺部多形性脂肪肉瘤。进行了手术，但无法进行根治性切除。术后放疗（40戈伊）与顺铂（12.5 mg/d，连用10 d）同步治疗，短期内获得部分缓解。患者在手术后8个月死于播散性疾病。根据文献报告，肺脂肪肉瘤必须被归类为一种侵袭性高转移性疾病，对化疗和放疗均反应不良。(C)1997 Elsevier Science爱尔兰有限公司
Liposarcoma of the lung is extremely ran with only 11 cases previously reported. A case of a locally advanced pulmonary pleomorphic liposarcoma in a 49-year-old male is presented. Surgery was performed but radical resection was not possible. Post-operative radiotherapy (40 Gy) was given concurrently with cisplatin (12.5 mg daily for 10 days), A partial response of short duration was obtained. The patient died 8 months following surgery with disseminated disease. Based on reports in the literature, liposarcoma of the lung must be classified as an aggressive highly metastatic disease responding poorly to both chemotherapy and radiotherapy. (C) 1997 Elsevier Science Ireland Ltd.