Arnautovic K I, Husain M M, Linskey M E
Department of Neurological Surgery, University of Arkansas for Medical Sciences, Little Rock 72205, USA.
J Neurooncol. 2000 Sep;49(3):205-12. doi: 10.1023/a:1006488905526.
With the exception of patients with neurofibromatosis type II, pediatric extraparenchymal cerebellopontine angle (CPA) tumors of any sort are extremely rare. Most gliomas encountered in the CPA in either children or adults involve the CPA as exophytic extensions of primary brain stem and/or cerebellar tumors. We encountered an unusual case of a giant CPA pilocytic astrocytoma arising from the proximal trigeminal nerve, completely separate from the brain stem. A nine-year-old girl with no evidence for any neurocutaneous syndrome, presented with headaches, mild obstructive hydrocephalus, trigeminal hypesthesia and a subtle peripheral facial paresis. Pre-operative neuroimaging suggested a petroclival meningioma. The tumor was completely resected via a right pre-sigmoid, retro-labyrinthine, subtemporal, transtentorial ('petrosal') approach, using intraoperative neurophysiological monitoring, with minimal morbidity. This appears to be the first reported case of a pediatric primary CPA glioma and the seventh reported case of primary CPA glioma, overall. It represents the second reported case of a primary CPA pilocytic astrocytoma. Given the findings in this case and the six other cases of primary CPA gliomas reported in the literature, as well as the results of histological studies of normal cranial nerves, we hypothesize that the point of origin of these rare and unusual tumors is the root entry zone of the involved cranial nerves. The differential diagnosis of primary CPA tumors should be expanded to include cranial nerve root entry zone primary CPA gliomas.
除II型神经纤维瘤病患者外,小儿任何类型的脑桥小脑角(CPA)实质外肿瘤都极为罕见。儿童或成人CPA中遇到的大多数胶质瘤是作为原发性脑干和/或小脑肿瘤的外生性延伸累及CPA。我们遇到了一例不寻常的巨大CPA毛细胞型星形细胞瘤,起源于三叉神经近端,与脑干完全分离。一名9岁女孩,无任何神经皮肤综合征证据,表现为头痛、轻度梗阻性脑积水、三叉神经感觉减退和轻微的周围性面瘫。术前神经影像学检查提示为岩斜区脑膜瘤。通过右侧乙状窦前、迷路后、颞下、经小脑幕(“岩骨”)入路,在术中神经生理监测下将肿瘤完全切除,术后并发症极少。这似乎是首例报道的小儿原发性CPA胶质瘤,也是总体上第7例报道的原发性CPA胶质瘤。它代表了第二例报道的原发性CPA毛细胞型星形细胞瘤。根据该病例及文献中其他6例原发性CPA胶质瘤的研究结果,以及正常颅神经的组织学研究结果,我们推测这些罕见且不寻常肿瘤的起源点是受累颅神经的神经根入区。原发性CPA肿瘤的鉴别诊断应扩大到包括颅神经根入区原发性CPA胶质瘤。