Department
Neurology; Neuroscience
Document Type
Article
Abstract
We describe the case of a 59-year-old woman who presented with progressive bilateral vestibular hypofunction and who was found to have bilateral granulomatous mass lesions of the mesial temporal lobe. Initially, her condition stabilized neurologically with corticosteroids, but a diagnosis of neurosarcoidosis was delayed because of the unusual presentation and persistently normal chest imaging results and serum angiotensin-converting enzyme (ACE) levels. Approximately 1 year after her initial presentation, the patient died of complications of a myocardial infarction and pulmonary embolism. Sarcoidosis should be considered in the differential diagnosis of idiopathic bilateral vestibular hypofunction even if the chest imaging and serum ACE levels are normal, particularly when there is evidence of a multisystem process.
Medical Subject Headings
neurology
Publication Date
2011
Publication Title
Ear, Nose and Throat Journal
ISSN
0145-5613
Volume
90
Issue
1
First Page
2
Last Page
15
PubMed ID
21229491
Digital Object Identifier (DOI)
10.1177/014556131109000111
Recommended Citation
Smith, Jonathan H.; Stovall, Kyndra C.; Coons, Stephen W; and Fife, Terry D., "Bilateral Vestibular Hypofunction in Neurosarcoidosis: A Case Report" (2011). Neurology. 56.
https://scholar.barrowneuro.org/neurology/56