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IgG4-Related Hypertrophic Pachymeningitis
JAMA Neurol 71:785-793, Lu, L.X.,et al, 2014
See this aricle in Pubmed

Article Abstract
IgG4-related disease accounts for an increasing proportion of cases of idiopathic hypertrophic pachymeningitis. Clinicians should become familiar with this alternative differential diagnosis because a prompt, specific therapeutic approach may avoid long-term neurological complications.
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cerebrospinal fluid,abnormal
cerebrospinal fluid,oligoclonal IgG in
cranial nerve palsies
hypertrophic intracranial pachymeningitis
hypertrophic pachymeningitis,IgG4 related disease
IgG4-related disease
neurologic disease,diagnoses of
pleocytosis of cerebrospinal fluid
review article
steroid therapy,CNS treatment and complications with
treatment of neurologic disorder

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