Idiopathic hypertrophic pachymeningitis mimicking neurosarcoidosis

Serum labs were all unremarkable, and included an ACE level, VDRL, Lyme disease titer and HIV ELISA, PCRs for HSV, VZV and enteroviridae, mycology and acid fast bacilli smears and cultures, extractable nuclear antibodies panel (Anti-RNP, Anti-Sm, Anti-SS-A, Anti-SS-B, Scl-70, Anti-Jo-1), acetylcholi...

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Published inClinical neurology and neurosurgery Vol. 114; no. 2; pp. 176 - 178
Main Authors Christakis, Panos G, Machado, Duarte G, Fattahi, Pooia
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.02.2012
Elsevier
Elsevier Limited
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Summary:Serum labs were all unremarkable, and included an ACE level, VDRL, Lyme disease titer and HIV ELISA, PCRs for HSV, VZV and enteroviridae, mycology and acid fast bacilli smears and cultures, extractable nuclear antibodies panel (Anti-RNP, Anti-Sm, Anti-SS-A, Anti-SS-B, Scl-70, Anti-Jo-1), acetylcholine receptor antibody, ANA, ANCA, cryoglobulin, and cardiolipin antibody tests, hepatitis panel and thyroid function tests. Contrast-enhanced MRI imaging typically demonstrates thickened dura, and symptoms are thought to be as a result of fibrous entrapment or ischemic damage of neurovascular structures [1-3].\n However, failure to correctly identify and treat primary etiologies such as infection and malignancy may have devastating consequences, and inadequate treatment of IHP may result in irreversible vision loss, status epilepticus, and paralysis [1,2].
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ObjectType-Report-1
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ISSN:0303-8467
1872-6968
DOI:10.1016/j.clineuro.2011.10.011