| Literature DB >> 29650638 |
Michal Lubomski1,2, James Dalgliesh3, Kenneth Lee4, Omprakash Damodaran5, Genevieve McKew6,7, Stephen Reddel1,7.
Abstract
A 63-year-old man presented with a 2-month history of progressive right-sided exophthalmos, painful ophthalmoplegia and fevers. As more features developed, he was diagnosed with giant cell arteritis, then Tolosa-Hunt syndrome, and transiently responded to corticosteroids. A bland cerebrospinal fluid and highly metabolically active brain (18F)-fluoro-D-glucose-positron emission tomography suggested lymphoma. Biopsy of the mass showed sulphur granules with Gram-positive filamentous bacteria with Actinomyces-like colonies. Actinomyces cavernous sinus infections are rare and indolent. They often mimic non-infective causes including other inflammatory and infiltrative conditions, vascular and neoplastic causes, particularly lymphoma. Clinicians should consider infective cavernous sinus syndromes in people with a fluctuating painful ophthalmoplegia that responds poorly to corticosteroids. The term Tolosa-Hunt syndrome is problematic and should be retired or used only with reservation. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: actinomyces; cavernous sinus; infection; ophthalmoplegia; tolosa-hunt syndrome
Mesh:
Year: 2018 PMID: 29650638 DOI: 10.1136/practneurol-2017-001844
Source DB: PubMed Journal: Pract Neurol ISSN: 1474-7758