Dropcho E J, Allen J C
Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.
J Neurooncol. 1987;5(2):139-50. doi: 10.1007/BF02571302.
Invasion of the meninges is a relatively common complication of head and neck rhabdomyosarcoma (RMS), while RMS arising primarily within the brain or meninges is rare. We report the case of an 11-year old child with a primary "primitive" frontal lobe tumor, subsequent leptomeningeal spread and fatal intratumoral hemorrhage; the diagnosis of RMS was discovered only at postmortem examination. The literature contains a total of 34 reported cases of primary intracranial RMS. This tumor has been observed to arise in a variety of central nervous system (CNS) locations in patients of all ages, but most commonly within the posterior fossa of children. Leptomeningeal dissemination and spontaneous intratumoral hemorrhage are important clinical features. Postoperative chemotherapy and craniospinal radiation may improve the anticipated poor prognosis of patients treated with surgery and radiation alone. The diagnosis of RMS may be missed unless electron microscopic and specific immunohistochemical studies are applied to "undifferentiated" or "primitive" CNS tumors.
脑膜侵犯是头颈部横纹肌肉瘤(RMS)相对常见的并发症,而主要起源于脑或脑膜内的RMS则较为罕见。我们报告了一例11岁儿童,患有原发性“原始”额叶肿瘤,随后出现软脑膜播散和致命的肿瘤内出血;RMS的诊断仅在尸检时才发现。文献中总共报道了34例原发性颅内RMS病例。已观察到该肿瘤可发生于各年龄段患者的多种中枢神经系统(CNS)部位,但最常见于儿童的后颅窝。软脑膜播散和自发性肿瘤内出血是重要的临床特征。术后化疗和全脑全脊髓放疗可能会改善单纯手术和放疗患者预期较差的预后。除非对“未分化”或“原始”CNS肿瘤进行电子显微镜检查和特异性免疫组化研究,否则可能会漏诊RMS。