A case of ANCA associated vasculitis presented with mononeuritis multiplex

Authors

  • Tanbin Rahman Registrar, Medicine, Greenlife Medical College and Hospital, Dhaka, Bangladesh
  • Md Rashedul Islam Assistant Professor, Department of Neurology, BIRDEM General Hospital, Dhaka, Bangladesh
  • Mohammad Sakhawat Hossen Khan Registrar, Department of Neurology, BIRDEM General Hospital, Dhaka, Bangladesh
  • Sharif Mohammad Ruhul Quddus Assistant Registrar, Department of Neurology, BIRDEM General Hospital, Dhaka, Bangladesh
  • Dilruba Alam Registrar, Department of Neurology, BIRDEM General Hospital, Dhaka, Bangladesh
  • Rumana Habib Associate Professor, Department of Neurology, BIRDEM General Hospital, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/birdem.v9i3.43094

Keywords:

ANCA associated vasculitis, eosinophilic granulomatosis with polyangiitis, microscopic polyangiitis, granulomatosis with polyangiitis

Abstract

Mononeuritis multiplex is a common manifestation of many illnesses which includes diabetes, leprosy, malignancy and certain types of systemic vasculitis. The antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of rare diseases which show typical characteristic inflammatory cell infiltration and blood vessel wall necrosis. AAV syndromes include granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA) and eosinophilicgranulomatosis with polyangiitis (EGPA). Here we present a patient who presented with mononeuritis multiplex and had features ofEGPA. The patient was treated with standard regimen of steroids and pulsed cyclophosphamide and she achieved good clinical response.

Birdem Med J 2019; 9(3): 257-260

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Published

2019-09-11

How to Cite

Rahman, T., Islam, M. R., Khan, M. S. H., Quddus, S. M. R., Alam, D., & Habib, R. (2019). A case of ANCA associated vasculitis presented with mononeuritis multiplex. BIRDEM Medical Journal, 9(3), 257–260. https://doi.org/10.3329/birdem.v9i3.43094

Issue

Section

Case Reports