ArticleCureus2024
Cerebellar Mutism Syndrome in a Patient With Hypertensive Urgency and Ischemia: A Case Report.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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2 authors.
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Abstract
Cerebellar mutism syndrome (also known as posterior fossa syndrome) has been mostly seen in pediatric patients after surgery for neoplastic disease and is characterized by mutism, with variable symptoms such as emotional lability, ataxia, apraxia, and hypotonia. While the mechanism is not precisely defined, it is thought to result from disconnections between the cortical and cerebellar brain networks. Presentation in adult patients is rare, with various etiologies including posterior fossa ischemia, hemorrhage, and tumors being most reported. We report a case of adult-onset posterior fossa syndrome in a woman with a previous right hemisphere cerebellar stroke, in the context of contralateral cerebellar involvement and hypertensive urgency. The etiology, clinical presentation and course, and management of posterior fossa syndrome are discussed.
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