Hypertrophic Pachymeningitis from Neuro-Behçet’s Disease: A Case Report

Authors

  • Suntaree Thitiwichienlert Department of Ophthalmology, Faculty of Medicine, Thammasat University
  • Dussadee Sakonlaya Department of Pathology and Forensic Medicine, Faculty of Medicine, Thammasat University
  • Panlop Chakkavittumrong Department of Dermatology, Faculty of Medicine, Thammasat University
  • Punchong Hanvivadhanakul Department of Rheumatology, Faculty of Medicine, Thammasat University
  • Supinda Leeamornsiri Department of Ophthalmology, Faculty of Medicine, Thammasat University
  • Wimolwan Tangpagasit Department of Ophthalmology, Faculty of Medicine, Thammasat University
  • Thanapat Dechasasawat Department of Radiology, Faculty of Medicine, Thammasat University

Keywords:

Optic Neuritis, Pachymeningitis, Behçet’s Disease

Abstract

A 26-year-old female presented with visual loss for 10 days from optic neuritis, which had recurred in the fellow eye one year apart. Neuroimaging, Pathergy test and skin biopsy results supported the diagnosis of neuro-Behçetʼs disease. The patient was successfully treated with pulse methylprednisolone followed by prednisolone and immunosuppressive agents.

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References

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Published

2024-08-31

How to Cite

[1]
Thitiwichienlert, S. , Sakonlaya, D., Chakkavittumrong, P., Hanvivadhanakul, P., Leeamornsiri, S., Tangpagasit, W. and Dechasasawat, T. 2024. Hypertrophic Pachymeningitis from Neuro-Behçet’s Disease: A Case Report. Asian Medical Journal and Alternative Medicine. 24, 2 (Aug. 2024), 64–69.

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Section

Case Report