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