1.IgG4-Related Intracranial Hypertrophic Pachymeningitis : A Case Report and Review of the Literature.
Satoru TAKEUCHI ; Hideo OSADA ; Soichiro SENO ; Hiroshi NAWASHIRO
Journal of Korean Neurosurgical Society 2014;55(5):300-302
Hypertrophic pachymeningitis is an uncommon disorder that causes a localized or diffuse thickening of the dura mater. Recently, the possibility that IgG4-related sclerosing disease may underlie some cases of intracranial hypertrophic pachymeningitis has been suggested. We herein report the tenth case of IgG4-related intracranial hypertrophic pachymeningitis and review the previous literature. A 45-year-old male presented with left-sided focal seizures with generalization. Magnetic resonance imaging (MRI) revealed a diffuse thickening and enhancement of the right convexity dura matter and falx with focal nodularity. The surgically resected specimens exhibited the proliferation of fibroblast-like spindle cells and an infiltration of mononuclear cells, including predominantly plasma cells. The ratio of IgG4-positive plasma cells to the overall IgG-positive cells was 45% in the area containing the highest infiltration of plasma cells. On the basis of the above findings, IgG4-related sclerosing disease arising from the dura mater was suspected. IgG4-related sclerosing disease should be added to the pachymeningitis spectrum.
Dura Mater
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Generalization (Psychology)
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Humans
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Immunohistochemistry
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Magnetic Resonance Imaging
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Male
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Meningitis*
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Middle Aged
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Plasma Cells
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Seizures