Severe IgA vasculitis with features of remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome in a 60‐year‐old male treated with plasmapheresis-Reference-Cited by-同舟云学术

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Severe IgA vasculitis with features of remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome in a 60‐year‐old male treated with plasmapheresis

Published:2022-02-15 Issue:2 Volume:2 Page:98-101
ISSN:2767-1429
Container-title:Rheumatology & Autoimmunity
language:en
Short-container-title:Rheumatology & Autoimmunity

Author:

Mathew Shawn¹,Goyal Rohan²,Gupta Nealansh¹,Joks Rauno³

Affiliation:

1. Internal Medicine, Ringgold Standard Institution SUNY Downstate Health Sciences University Brooklyn New York USA

2. SUNY Downstate Medical Center College of Medicine Ringgold Standard Institution Brooklyn New York USA

3. Allergy and Immunology, Center for Allergy and Asthma Research SUNY Downstate Health Sciences University Brooklyn New York USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rai2.12007

Reference22 articles.

1. IgA Vasculitis in Adults

2. Incidence of IgA vasculitis in the adult Slovenian population

3. Incidence of IgA vasculitis in children estimated by four-source capture–recapture analysis: a population-based study

4. Cardiovascular, thromboembolic and renal outcomes in IgA vasculitis (Henoch-Schönlein purpura): a retrospective cohort study using routinely collected primary care data

5. Late‐onset IgA vasculitis in adult patients exhibits distinct clinical characteristics and outcomes;Hong S;Clin Exp Rheumatol,2016

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