Ritter J, Caesar R, Ostapowicz G, Oehme J
Monatsschr Kinderheilkd (1902). 1978 Apr;126(4):209-11.
A patient with abdominal liposarcoma is described, and the treatment of this in children extremely uncommon tumor is discussed. After complete surgical excision, local irradion with 5000-6000 rad should be considered only if no vital organs are irradiated. Because of the high tendency for local recurrence and for distant metastases of this tumor a primary polychemotherapy beginning immediately after surgical excision is proposed as in cases of other solid tumors in children for instance rhabdomyosarcoma or fibrosarcoma. 18 months after the surgical excision and after the beginning of polychemotherapy our patient is clinically well without demonstrable tumor growth.
本文描述了一名患有腹部脂肪肉瘤的患者,并讨论了这种在儿童中极为罕见的肿瘤的治疗方法。在完全手术切除后,仅当不照射重要器官时,才应考虑进行5000 - 6000拉德的局部放疗。由于这种肿瘤局部复发和远处转移的倾向很高,建议在手术切除后立即开始进行一线多药化疗,就像儿童其他实体瘤(如横纹肌肉瘤或纤维肉瘤)的情况一样。手术切除和开始多药化疗18个月后,我们的患者临床状况良好,未发现肿瘤生长。