| Literature DB >> 21285896 |
Charles Shyu1, Kelly Burke, Mark M Souweidane, Ira J Dunkel, Stephen W Gilheeney, Timothy Gershon, Yasmin Khakoo.
Abstract
Cerebellar mutism syndrome (CMS) is a complication of posterior fossa surgery seen primarily in pediatric patients after resection of medulloblastoma. CMS is characterized by mutism, ataxia, hypotonia, and irritability. Currently, there is no therapy of proven efficacy. Zolpidem, although primarily used as a sedative, has been shown to alleviate mutism and promote arousal in similar neurologic and psychiatric disorders. Here, we describe a child with severe CMS in whom zolpidem seemed to increase arousal, accelerate the resolution of mutism, and decrease emotional lability. Our report suggests that clinicians should consider using zolpidem for patients with CMS.Entities:
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Year: 2011 PMID: 21285896 DOI: 10.1097/MPH.0b013e3182053a1a
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289