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Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-766675

RESUMO

Immunoglobulin G4-related hypertrophic pachymeningitis (IgG4-RHP) is an increasingly recognized manifestation of IgG4-related disease (IgG4-RD), which is a fibroinflammatory condition that can affect virtually any organ. The three hallmark histopathological features of IgG4-RD are lymphoplasmacytic infiltration of IgG4-positive plasma cells, storiform fibrosis, and obliterative phlebitis. We report a case of biopsy-confirmed IgG4-RHP that was initially misdiagnosed as cerebral venous thrombosis.


Assuntos
Fibrose , Imunoglobulinas , Trombose Intracraniana , Meningite , Flebite , Plasmócitos , Trombose Venosa
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