Sharma Rewati Raman, Netalkar Audumbar S, Pawar Sanjay J, Lad Santosh D, Musa Mohammed M, Mahapatra Ashok Kumar
National Neurosurgical Center, Khoula Hospital, Sultanate of Oman.
J Clin Neurosci. 2002 Jan;9(1):97-9. doi: 10.1054/jocn.2001.0948.
Intracranial schwannomas commonly arise from the vestibular nerve and less commonly from other cranial nerves. On rare occasions, they may be intraparenchymatous, intraventricularor intrasellar. However, the occurrence of a congenital solitary intracranial extradural schwannoma unrelated to any cranial nerve in the absence of von Recklinghausan's syndrome is exceptional. The authors report a unique, heretofore unreported case of a congenital temporal extradural schwannoma, unassociated with any known cranial nerve and with a transcranial extension presenting as a temporal fossa mass since birth in a 16-year-old female patient. Total resection of this tumour was uncomplicated. A brief review of the relevant literature is presented.
颅内神经鞘瘤通常起源于前庭神经,较少起源于其他颅神经。在极少数情况下,它们可能位于脑实质内、脑室内或鞍内。然而,在没有冯·雷克林豪森综合征的情况下,发生与任何颅神经无关的先天性孤立性颅内硬膜外神经鞘瘤是罕见的。作者报告了一例独特的、迄今未报道的先天性颞部硬膜外神经鞘瘤病例,该肿瘤与任何已知颅神经无关,自出生以来经颅扩展表现为颞窝肿块,患者为一名16岁女性。该肿瘤的全切除过程顺利。本文对相关文献进行了简要综述。