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J Korean Neurosurg Soc. 1992 May;21(5):586-592. Korean. Original Article.
Yun H , Ko Y , Bak KH , Park CW , Lee U , Park SH , Park HR .
Department of Neurosurgery, Chung Ang Gil Hospital, Incheon, Korea.
Department of Pathology, Chung Ang Gil Hospital, Incheon, Korea.
Abstract

The authors present a case of central neurocytoma in right lateral ventricle. Central neurocytoma is a rare clinicopathological entity that has been recently recognized and is characterized by 1) intraventricular location, 2) predominant occurance in young adults, 3) oligodendroglioma-like histology, 4) benign course, 5) immunohistochemical and ultrastructual evidence of neuronal differentiation. Twenty one year old female patient was admitted to the Department of neurosurgery of Chung Ang Gil hospital because of diplopia and headache which developed and progressed gradually 2 months prior to admission. The neurological examination showed paresis of right lateral rectus muscle, bilateral optic papilledema, nystagmus and mild left hemiparesis. MRI scan showd an intraventricular tumor of lateral ventricle that had isosignal and high signal intensity with cortex on T1-and T2-weighted and proton density images, respectively. Serpiginous flow voids representing blood vessels in the tumor were seen an all pulse sequences.

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