Bouffet E, Frappaz D, Dolbeau D, Sobol H, Jouvet A, Carrie C, Pondarre C, Brunat-Mentigny M, Philip T, Mottolese C
Pediatric Unit, Centre Léon Bérard, Lyon, France.
J Neurooncol. 1993 Jul;17(1):65-70. doi: 10.1007/BF01054275.
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.
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。