Abstract
Reversible splenial lesion syndrome (RESLES) is a rare clinico–radiological entity characterized by transient lesions involving the splenium of the corpus callosum (SCC). It has been described in a broad spectrum of conditions. We report the case of a RESLES in a young woman ultimately diagnosed with fulminant idiopathic intracranial hypertension (IIH). To the best of our knowledge, this is the first such association reported.
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