| Literature DB >> 28273992 |
Ravi Anadure1, Coimbatore Narayanan2, Govindraj Varadraj3, Bevinahalli Nandeesh4.
Abstract
Mononeuritis multiplex is a common manifestation of many illnesses which includes Hansen's disease 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 Eosinophilic Granulomatosis with Polyangiitis (EGPA). We describe a patient who presented with mononeuritis multiplex and had features of overlap between EGPA and MPA. The patient was treated with standard regimen of steroids and pulsed cyclophosphamide and she achieved excellent clinical remission.Entities:
Keywords: ANCA Associated Vasculitis; Eosinophilic Granulomatosis with Polyangiitis; Microscopic Polyangiitis
Year: 2017 PMID: 28273992 PMCID: PMC5324437 DOI: 10.7860/JCDR/2017/22252.9149
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X