| Literature DB >> 30617191 |
Sucharita Anand1, Animesh Das1, Surjyaprakash Shivnarayan Choudhury1.
Abstract
A 26-year-old patient of limited cutaneous sclerosis presented to us with insidious-onset posterior fossa symptoms of headache, vomiting, vertigo and gait imbalance, progressing over a period of 3 weeks. A diagnosis of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids was made by combining the clinical features with radiological evidence showing punctate infiltration of the pons, brainstem and cerebellum. Relevant differentials in the form of neurosarcoid, infections, central nervous system (CNS) lymphoma and Neuro-Behcet's disease were ruled out by history and investigations. The patient responded dramatically to steroid therapy, and had no neurological deficits after 18 months of follow-up. This case highlights the rare association of a not-so-common immunological disease with a rare neurological disease. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: brain stem/cerebellum; neuroimaging; neurology (drugs and medicines)
Mesh:
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Year: 2019 PMID: 30617191 PMCID: PMC6326288 DOI: 10.1136/bcr-2018-226259
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X