Recurrent adult onset Henoch-Schonlein Purpura: a case report.

TitleRecurrent adult onset Henoch-Schonlein Purpura: a case report.
Publication TypeJournal Article
Year of Publication2016
AuthorsGaskill N, Guido B, Magro C
JournalDermatol Online J
Volume22
Issue8
Date Published2016 08 15
ISSN1087-2108
KeywordsAdult, Diagnosis, Differential, Female, Fluorescent Antibody Technique, Direct, Glomerulonephritis, IGA, Humans, Immunoglobulin A, Nephritis, Purpura, Schoenlein-Henoch, Recurrence, Skin
Abstract

Henoch-Schonlein purpura is an immunoglobulin A (IgA)-immune complex mediated leukocytoclastic vasculitis that classically manifests with palpable purpura, abdominal pain, arthritis, and hematuria or proteinuria. The condition is much more predominant in children (90% of cases) and commonly follows an upper respiratory infection. We present a case of recurrent Henoch-Schonlein purpura (HSP) complicated by nephritis in an adult female initially categorized as IgA nephropathy (IgAN). We review the pathophysiologic basis of HSP nephritis as the variant of HSP accompanied by renal involvement and its pathogenetic commonality with IgA nephropathy.

Alternate JournalDermatol Online J
PubMed ID27617937
Related Faculty: 
Cynthia M. Magro, M.D.

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