Oculomotor Nerve Schwannoma: A Case Report

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Oculomotor Nerve Schwannoma: A Case Report

Schwannomas account for about 8% of intracranial tumors and 90% are vestibular schwannomas. Oculomotor schwannoma without neurofibromatosis is extremely rare. A 41-year-old female presented with complaints of blurred vision, and the neurologic examination revealed afferent pupillary defect and decreased visual acuity of the left side. Brain magnetic resonance image showed an extra axial mass in...

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Oculomotor Nerve Schwannoma Associated with Acute Hydrocephalus: Case Report

A 37-year-old woman presented with an extremely rare large oculomotor schwannoma associated with acute hydrocephalus manifesting as semicoma and anisocoria. Brain computed tomography and magnetic resonance imaging revealed a tumor in the oculomotor cistern. Cerebral angiography revealed separation of the posterior cerebral artery (PCA) and superior cerebellar artery (SCA). The tumor was removed...

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Schwannoma of the oculomotor nerve.

A 63-year-old woman presented with an extremely rare oculomotor schwannoma not associated with neurofibromatosis, manifesting as a transient diplopia and ptosis. Magnetic resonance images showed a well-enhanced mass extending from the cavernous sinus to the intraorbital region. Surgical exposure confirmed the tumor originating from the oculomotor nerve in the cavernous sinus. The intraorbital c...

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[Intraparotid facial nerve schwannoma: a case report].

OBJECTIVE We describe a case of intraparotid facial nerve schwannoma. About sixty patients with intraparotid tumors have been reported in the literature. MATERIAL AND METHODS A 89-year-old female patient presented with a history of progressive facial palsy and a left intraparotid mass. The mass was removed by parotidectomy for definitive diagnosis and treatment. We reviewed the findings in co...

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Intraparotid facial nerve schwannoma: A case report

Introduction: Intraparotid facial nerve schwannoma is a rare tumor accounting for only 0.2 – 1.5 % of all parotid tumors. We present this case because this tumor grows slowly and rarely produces signs and symptoms thus mimicking pleomorphic adenoma which is much more common. When it is diagnosed peroperatively the management differs significantly and is a matter of debate with few favoring comp...

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ژورنال

عنوان ژورنال: Brain Tumor Research and Treatment

سال: 2014

ISSN: 2288-2405,2288-2413

DOI: 10.14791/btrt.2014.2.1.43