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자료유형
학술저널
저자정보
Takeuchi, Satoru (Department of Neurosurgery, National Defense Medical College) Osada, Hideo (Department of Neurosurgery, National Defense Medical College) Seno, Soichiro (Department of Neurosurgery, National Defense Medical College) Nawashiro, Hiroshi (Department of Neurosurgery, National Defense Medical College)
저널정보
대한신경외과학회 대한신경외과학회지 대한신경외과학회지 제55권 제5호
발행연도
2014.1
수록면
300 - 302 (3page)

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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.

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