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Complete ophthalmoplegia: A rare presentation of idiopathic intracranial hypertension

Idiopathic intracranial hypertension (IIH) is a disorder defined by clinical criteria that include signs and symptoms isolated to those produced by increased intracranial pressure (ICP; e. g., headache, papilledema, and vision loss), elevated ICP with normal cerebrospinal fluid (CSF) composition, an...

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Detalles Bibliográficos
Autores principales: Wani, Irfan Yousuf, Verma, Sawan, Wani, Mushtaq, Asimi, Ravouf, Sheikh, Saleem, Wani, Maqbool, Sheikh, Nawaz, Shah, Irfan, Mushtaq, Mudasir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683894/
https://www.ncbi.nlm.nih.gov/pubmed/26713027
http://dx.doi.org/10.4103/0972-2327.160087
Descripción
Sumario:Idiopathic intracranial hypertension (IIH) is a disorder defined by clinical criteria that include signs and symptoms isolated to those produced by increased intracranial pressure (ICP; e. g., headache, papilledema, and vision loss), elevated ICP with normal cerebrospinal fluid (CSF) composition, and no other cause of intracranial hypertension evident on neuroimaging or other evaluations. The most common signs in IIH are papilledema, visual field loss, and unilateral or bilateral sixth cranial nerve palsy. Here we report a case of IIH presenting as headache with vision loss, papilledema, complete ophthalmoplegia with proptosis in one eye, and sixth cranial nerve palsy in the other eye. Patient was managed with acetazolamide, topiramate, and diuretics. Symptoms remained static and she was planned for urgent CSF diversion procedure.