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Pediatric Rheumatology
Published in: Pediatric Rheumatology 1/2013

Open Access 01-11-2013 | Meeting abstract

P03-011 - Differential for granulomatosis with polyangiitis

Authors: SM Rawn, P Miettunen, H Schmeling

Published in: Pediatric Rheumatology | Special Issue 1/2013

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Excerpt

Granulomatosis with Polyangiitis (GPA) is a rare and potentially lethal vasculitis, which predominantly affects small vessels. GPA can present with palpable purpura, hemorrhagic macules and bullae similar to skin lesions found in the most common small vessel vasculitis in childhood, Henoch-Schoenlein Purpura (HSP), leading to diagnostic confusion. …
Literature
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Twilt M, Benseler S, Cabral D: Granulomatosis with Polyangiitis in Childhood. Curr Rheumatol Rep. 2012, 14: 107-115.CrossRefPubMed
2.
Ruperto N, Ozen S, Pistorio A, Dolezalova P, Brogan P: EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation. Ann Rheum Dis. 2012, 69: 790-797.CrossRef
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Marzano AV, Vezzoli P, Berti E: Skin involvement in cutaneous and systematic vasculitis. Autoimmun Rev. 2012, [Epub ahead of print]
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Deng F, Lu L, Zhang Q, Hu B, Wang SJ, Huang N: Henoch-Schonlein purpura in childhood: treatment and prognosis. Analysis of 425 cases over a 5-year period. Clin Rheumatol. 2010, 29: 369-74.CrossRefPubMed
Metadata
Title
P03-011 - Differential for granulomatosis with polyangiitis
Authors
SM Rawn
P Miettunen
H Schmeling
Publication date
01-11-2013
Publisher
BioMed Central
Published in
Pediatric Rheumatology / Issue Special Issue 1/2013
Electronic ISSN: 1546-0096
DOI
https://doi.org/10.1186/1546-0096-11-S1-A207

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