A case report of meningeal Rosai-Dorfman disease associated with IgG4-related disease

Clin Neuropathol. 2015 Nov-Dec;34(6):343-9. doi: 10.5414/NP300871.

Abstract

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.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Autoimmune Diseases / complications
  • Autoimmune Diseases / immunology*
  • Biopsy
  • Diagnosis, Differential
  • Emperipolesis / immunology
  • Female
  • Histiocytosis, Sinus / diagnosis
  • Histiocytosis, Sinus / etiology
  • Histiocytosis, Sinus / pathology*
  • Humans
  • Immunoglobulin G / immunology*
  • Meninges / pathology*
  • Plasma Cells / pathology*

Substances

  • Immunoglobulin G