Polivka M, Lot G, Woimant F, Vaunaize J, Leclerc Y, Mikol J
Service d'Anatomie Pathologique, Hôpital lariboisière, Paris.
Ann Pathol. 1993;13(2):118-22.
A patient, aged 26, had a large parietal tumor, clinically revealed by intracranial hypertension and left sized paresthesia. Removal of tumor was followed by a rapid recurrence. Rhabdomyosarcoma was diagnosed on the second surgical specimen. These tumors are rare in the central nervous system. They occur mostly, though not exclusively, in young adults. Their prognosis is poor and their histogenesis is still unclear.
一名26岁患者患有巨大顶叶肿瘤,临床上表现为颅内高压和左侧感觉异常。肿瘤切除后迅速复发。第二次手术标本诊断为横纹肌肉瘤。这些肿瘤在中枢神经系统中很少见。它们大多发生于年轻人,但并非仅见于年轻人。其预后较差,组织发生仍不清楚。