01218nas a2200169 4500000000100000008004100001100001400042700001600056700001500072700001500087245008100102856007800183300001400261490000700275520075200282022001401034 2017 d1 aAnadure R1 aNarayanan C1 aVaradraj G1 aNandeesh B00aANCA Associated Mononeuritis Multiplex with Overlap in Vasculitic Syndromes. uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324437/pdf/jcdr-11-OD01.pdf aOD01-OD030 v113 a

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.

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