Peeples W J, Hazra T
Urology. 1976 Jan;7(1):89-92. doi: 10.1016/0090-4295(76)90573-2.
Retroperitoneal liposarcoma is a rare tumor in children and has been reported previously on only three occasions. This is the fourth such case, presenting with a large mass on the left side which displaced the sigmoid and ureters to the right. The patient was treated with surgery, radiotherapy, and chemotherapy. She is alive and well more than four years after therapy was instituted. A review of the pertinent literature cites the need for radio- and chemotherapy especially when surgical removal is incomplete.
腹膜后脂肪肉瘤在儿童中是一种罕见肿瘤,此前仅有三次报道。这是第四例此类病例,表现为左侧有一巨大肿块,将乙状结肠和输尿管向右推移。该患者接受了手术、放疗和化疗。自开始治疗至今已过去四年多,她仍然健在且情况良好。对相关文献的回顾表明,尤其在手术切除不完全时,需要进行放疗和化疗。