Primary Vasculitis in Childhood: GPA and MPA in Childhood

Childhood onset anti-neutrophilic cytoplasmic antibody (ANCA) associated vasculitis (AAV) is a rare group of primary systemic vasculitides affecting medium and small blood vessels. AAV includes granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), eosinophilic granulomatosis with p...

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Main Authors: Mehul P. Jariwala (Author), Ronald M. Laxer (Author)
Format: Book
Published: Frontiers Media S.A., 2018-08-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Mehul P. Jariwala  |e author 
700 1 0 |a Mehul P. Jariwala  |e author 
700 1 0 |a Ronald M. Laxer  |e author 
245 0 0 |a Primary Vasculitis in Childhood: GPA and MPA in Childhood 
260 |b Frontiers Media S.A.,   |c 2018-08-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2018.00226 
520 |a Childhood onset anti-neutrophilic cytoplasmic antibody (ANCA) associated vasculitis (AAV) is a rare group of primary systemic vasculitides affecting medium and small blood vessels. AAV includes granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), eosinophilic granulomatosis with polyangiitis (EGPA), and renal limited ANCA vasculitis. These disorders are associated with severe clinical manifestations, frequent relapses and a high cumulative morbidity, and often present with multisystem involvement. Renal involvement is common in the pediatric age group, characterized by pauci-immune necrotizing and crescentic glomerulonephritis which frequently progresses to chronic kidney disease in adulthood. ANCAs against proteinase 3 (PR3-ANCA) or myeloperoxidase (MPO) (MPO-ANCA) remain the hallmark of AAV and are integral to the disease pathogenesis. Newer understanding of neutrophil extracellular traps and complement activation have provided better insights into disease pathogenesis. A pediatric vasculitis working group has developed and validated childhood vasculitis classification criteria and disease activity and damage scores. No specific pediatric treatment recommendations exist due to rare nature of the illness in pediatric population. Smaller case series have been published on the efficacy of adult treatment regimens in pediatric patients. The prognosis often remains guarded with frequent relapses and a high cumulative morbidity. The aim of this article is to provide a comprehensive review on pediatric AAV with a focus on recent observations regarding epidemiology, disease pathogenesis, treatment, and prognosis. 
546 |a EN 
690 |a childhood vasculitis 
690 |a microscopic polyangiitis 
690 |a granulomatosis with polyangiitis 
690 |a ANCA-associated vasculitis 
690 |a small vessel vasculitis 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 6 (2018) 
787 0 |n https://www.frontiersin.org/article/10.3389/fped.2018.00226/full 
787 0 |n https://doaj.org/toc/2296-2360 
856 4 1 |u https://doaj.org/article/2d0c76b9d7c84625a9b98ec9c4bd42c2  |z Connect to this object online.