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1.本文报告7例脂肪肉瘤。2.本瘤发病率较低而确诊者尤少,如提高病理诊断质量,则发现率可望提高。3.Enterline 等分类法(1960)较为全面,系我院所采用,即分为五型:(1)分化良好粘液样型。(2)分化不良粘液样型,(3)脂肪瘤样型,(4)粘液混合型及(5)非粘液型。 4.脂肪肉瘤临床表现不一,多见于中老年人,男性稍多于女性,以下肢、腹膜后、躯干多见。5.治疗须彻底手术切除,术后补充放射治疗。不能手术者行放射治疗,可获一定疗效。肿瘤量应达6000—9000伦,于30—50天内完成。
1. This article reports 7 cases of liposarcoma. 2. The incidence of this tumor is low and the number of diagnosed patients is particularly small. If the quality of pathological diagnosis is improved, the discovery rate is expected to increase. 3. Enterline and other classification methods (1960) are more comprehensive and are used in our hospital. They are divided into five types: (1) well-differentiated mucoid type. (2) poorly differentiated mucinous type, (3) lipomatous type, (4) mixed mucus type, and (5) non-mucinous type. The clinical manifestations of liposarcoma are different, more common in middle-aged and elderly men, slightly more than women, the lower limb, retroperitoneal, trunk more common. 5. The treatment must be completely surgical resection, postoperative radiation therapy. Can not be operated by radiation therapy, can obtain a certain effect. The tumor volume should reach 6000-9000L and be completed within 30-50 days.