“…The primary vasculitis diagnosed were Takayasu Arteritis ( n = 10) [ 17 , 19 , 36 , 39 , 40 , 43 , 49 , 52 , 54 , 59 ], Eosinophilic granulomatosis with polyangiitis (n = 9) [ 20 , 21 , 24 , 42 , 44 , 46 , 55 – 57 ], Granulomatosis with Polyangiitis ( n = 7) [ 13 , 25 , 32 , 45 , 47 , 51 , 53 ], Periarteritis Nodosa ( n = 5) [ 16 , 27 , 29 , 37 , 58 ], Behcet’s disease ( n = 4) [ 12 , 23 , 35 , 38 ], Henoch-Schönlein purpura ( n = 3) [ 15 , 28 , 31 ], Microscopic polyangiitis and Kawasaki Disease (two cases each) [ 11 , 18 ] and [ 22 , 30 ], Buerger’s disease and Cutaneous leukocytoclastic angiitis (one case each) [ 48 ] and [ 33 ].…”