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Clin Neuropathol ; 34(6): 343-9, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26308253

RESUMO

AIMS: Rosai-Dorfman disease is a rare entity that has been described as lymphadenopathy in young patients. Extranodal forms of this disease have been previously observed. The etiology of Rosai-Dorfman disease remains unknown, relationships with the IgG4-related sclerotic disease have been detected. Herein, a rare case of Rosai-Dorfman disease with meningeal involvement and IgG4-related sclerotic disease is reported. MATERIAL: A meningeal biopsy in a 35-year-old woman who had a 6-month history of intermittent headache was performed after MRI examination showing diffuse leptomeningeal enhancement without cerebral parenchymal involvement. RESULTS: A mixed infiltration of lymphocytes, plasma cells, and histiocytes exhibiting emperipolesis was identified. The stroma was fibrous. Immunohistochemical analysis revealed a high number of IgG4-positive plasma cells and a rate of IgG4/IgG-positive plasma cells higher than 50%. CONCLUSION: The pathological results in this patient with meningeal infiltration are suggestive of Rosai-Dorman disease associated with IgG4-related disease. This observation further confirms the link between these two entities.


Assuntos
Doenças Autoimunes/imunologia , Histiocitose Sinusal/patologia , Imunoglobulina G/imunologia , Meninges/patologia , Plasmócitos/patologia , Adulto , Doenças Autoimunes/complicações , Biópsia , Diagnóstico Diferencial , Emperipolese/imunologia , Feminino , Histiocitose Sinusal/diagnóstico , Histiocitose Sinusal/etiologia , Humanos
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