Schäfer H, Wellens W
Strahlentherapie. 1978 Aug;154(8):520-5.
Liposarcoma is a rare soft-tissue tumor. According to Enzinger, there are five subgoups. Histological criteria, the beginning, diagnostic and therapy of this tumor are represented. Results have been ascertained as follows, founded on eight cases of our own: 1. Adequate radical surgery and radiation therapy are needed in each case. 2. Recurrences are frequently, metastasition is rarely observed. 3. The prognosis is poor, if a recurrence appears within two years.
脂肪肉瘤是一种罕见的软组织肿瘤。根据恩津格的分类，有五个亚组。文中介绍了该肿瘤的组织学标准、发病情况、诊断及治疗方法。基于我们自己的八例病例，得出如下结果：1. 每例均需要进行充分的根治性手术和放射治疗。2. 复发很常见，转移很少见。3. 如果在两年内出现复发，预后较差。
