2016
DOI: 10.1111/1756-185x.12954
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Polyarteritis nodosa in north India: clinical manifestations and outcomes

Abstract: In comparison to classic PAN in other populations, classic PAN in north India is associated with higher neurological involvement and lower GI involvement.

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Cited by 17 publications
(25 citation statements)
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References 21 publications
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“…PAN is more common in males among adults while females are equally affected in children. [10][11][12][13][14][15] In the presented pediatric cohort there was a clear female predominance with twice as more girls being affected, and a male predominance in adult patients. However, the reason for this difference is not clear; this may be partly due to cutaneous PAN cases, which is more frequent in females.…”
Section: Discussionmentioning
confidence: 82%
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“…PAN is more common in males among adults while females are equally affected in children. [10][11][12][13][14][15] In the presented pediatric cohort there was a clear female predominance with twice as more girls being affected, and a male predominance in adult patients. However, the reason for this difference is not clear; this may be partly due to cutaneous PAN cases, which is more frequent in females.…”
Section: Discussionmentioning
confidence: 82%
“…The male/female (M/F) ratio was 0.5 in children while there was a clear male predominance in adults (M/F 4.5). The median age at disease onset was 11 (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16) in children and 33 (19-71) years in adults. Nineteen adult patients (86.4%) also fulfilled the Ankara 2008 criteria for PAN.…”
Section: Resultsmentioning
confidence: 99%
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“…The second reason is immune complexes mediating micro‐vascular diseases such as PAN. Sharma et al . reported 4 cases (14.8% of the cohort) with dilated cardiomyopathy as cardiac involvement in PAN.…”
Section: Discussionmentioning
confidence: 99%
“…Small vessels vasculitis includes two distinct categories based on pathogenesis: antineutrophil cytoplasm antibody (ANCA)‐associated vasculitis and immune complex‐associated vasculitis. ANCA‐associated vasculitis include granulomatosis with polyangiitis (GPA; previously known as Wegener's granulomatosis), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA; Churg‐Strauss syndrome) . Immune‐complex small‐vessel vasculitis include immunoglobulin A (IgA) vasculitis (Henoch‐Schonlein purpura), cryoglobulinemic vasculitis and hypocomplementemic urticarial vasculitis (anti‐C1q vasculitis).…”
Section: Introductionmentioning
confidence: 99%