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Brief Report

Intradiploic dermoid cyst: a rare cause of intracranial hypertension

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Pages 414-415 | Received 17 Nov 2012, Accepted 31 Aug 2013, Published online: 30 Sep 2013
 

Abstract

In this study, we report a rare case of intradiploic dermoid cyst in a patient who developed rapid symptoms of intracranial hypertension (ICH) that mimicked Pseudotumor cerebri syndrome clinically. A 25-year-old female presented with a history of headache, nausea, vertigo and blurred vision in the past 4 months. Images revealed a small supratentorial extradural intradiploic tumor. A midline occipital craniotomy was performed and total removal of the dermoid cyst was accomplished. Present case demonstrated that dermoid cysts can be considered an exceptionally rare basic cause of ICH.

Declaration of interest: The authors report no declarations of interest. The authors alone are responsible for the content and writing of the paper.

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