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转移性幕上恶性横纹肌样瘤的成功治疗

Successful treatment for a metastatic supratentorial malignant rhabdoid tumor.

作者信息

Bouffet E, Frappaz D, Dolbeau D, Sobol H, Jouvet A, Carrie C, Pondarre C, Brunat-Mentigny M, Philip T, Mottolese C

机构信息

Pediatric Unit, Centre Léon Bérard, Lyon, France.

出版信息

J Neurooncol. 1993 Jul;17(1):65-70. doi: 10.1007/BF01054275.

Abstract

The case of a boy with a familial history of Rendu-Osler disease, who successively developed a cerebellar pilocytic astrocytoma (at 3 years of age) and a metastatic supratentorial malignant rhabdoid tumor (at the age of 12 years) is reported. After a complete surgical removal, the CSF was cleared by 4 courses of chemotherapy, and the child received a craniospinal irradiation. He is currently alive and well 19 months after completion of the treatment. The authors discuss the ethiopathogeny of such intracranial tumors and argue for aggressive treatment.

摘要

报告了一名患有遗传性出血性毛细血管扩张症家族史的男孩病例,该男孩先后患小脑毛细胞型星形细胞瘤(3岁时)和幕上转移性恶性横纹肌样瘤(12岁时)。在肿瘤完全手术切除后,通过4个疗程的化疗清除脑脊液,该患儿接受了全脑全脊髓照射。目前,在完成治疗19个月后,他仍然健在且状况良好。作者讨论了此类颅内肿瘤的发病机制,并主张积极治疗。

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