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An unusual parasagittal tumour with acute blindness and response to cerebrospinal fluid shunting

Publication Type : Journal Article

Publisher : Elsevier BV

Source : Journal of Clinical Neuroscience

Url : https://doi.org/10.1016/j.jocn.2006.01.006

Keywords : Hemangiopericytoma, Lumboperitoneal shunting, Pseudotumor syndrome, Tumor apoplexy, Vision loss

Campus : Kochi

School : School of Medicine

Year : 2007

Abstract : We report a seven-year-old girl who presented with a sudden tumor apoplexy due to a parasagittal hemangiopericytoma. Following tumor excision, the child was noted to have bilateral optic nerve dysfunction and progressive papilledema, despite rapid overall neurological improvement. Based on the clinical features, we feel that this case represents an unusual form of visual deterioration related to impaired CSF absorption somehow precipitated by the acute tumour apoplexy. This unusual case of blindness responded significantly to CSF shunting. Several reports exist describing raised intracranial pressure with papilledema caused by nonthrombotic sinus occlusion due to tumors in proximity to the posterior superior sagittal sinus, torcular herophili and the jugular outlet. Communicating hydrocephalus, pseudotumor syndrome or intracranial venous sinus obstruction should be considered when otherwise inexplicable visual loss coexists with optic nerve dysfunction and papilledema. We emphasize the importance of a thorough search for the cause of visual loss.

Cite this Research Publication : A. Pillai, S. Kumar, A. Kumar, D. Panikar, An unusual parasagittal tumour with acute blindness and response to cerebrospinal fluid shunting, Journal of Clinical Neuroscience, Elsevier BV, 2007, https://doi.org/10.1016/j.jocn.2006.01.006

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