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IgG4 ‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report

  • Haj Mohamad Ebrahim Ketabforoush A
  • Bahadorinia M
  • Dolatshahi E
  • et al.
Clinical Case Reports (2022) 10(9)
DOI: 10.1002/ccr3.6324
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Abstract

Nervous system involvement in IgG4‐related systemic disease (IgG4‐RD) is rarely reported and manifests as hypertrophic pachymeningitis and hypophysitis. In this report, a 33‐year‐old woman with neurological manifestations was diagnosed with IgG4‐RD by biopsy. The patient showed improvement in symptoms after treatment.

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Haj Mohamad Ebrahim Ketabforoush, A., Bahadorinia, M., Dolatshahi, E., Nozarian, Z., & Abbasi Khoshsirat, N. (2022). IgG4 ‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report. Clinical Case Reports, 10(9). https://doi.org/10.1002/ccr3.6324

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