Baranzelli M C, Bouretz J C, Dusol F, Gosselin P, Demaille M C
Service d'Oncologie pédiatrique, Centre Oscar Lambret, Lille.
Presse Med. 1989 Jun 24;18(25):1245-8.
Multiple osteosarcoma is a rare tumour which usually has a poor prognosis. We report the case of a 14-year old girl who developed successively, at 2 1/2 years' interval, one osteosarcoma of the right radius bone, then one of the left radius bone. The tumours were strictly symmetrical. Each time, the patient was treated with chemotherapy of the Rosen type and underwent conservative surgery. At present, 5 years after the first treatment, she is in good health. This case is remarkable on several scores: chemotherapy was feasible and well tolerated, the multiple osteosarcoma had a favourable outcome, and conservative surgery of both radius bones gave satisfactory functional results.
多发性骨肉瘤是一种罕见的肿瘤，其预后通常较差。我们报告一例14岁女孩的病例，她在2年半的间隔时间里先后发生了右桡骨骨肉瘤，然后是左桡骨骨肉瘤。肿瘤严格对称。每次，患者均接受罗森（Rosen）型化疗并接受保守手术。目前，在首次治疗5年后，她身体健康。该病例在几个方面都很显著：化疗可行且耐受性良好，多发性骨肉瘤预后良好，双侧桡骨的保守手术取得了令人满意的功能结果。
