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Atypical Presentation of IgA Vasculitis in an Adult

Dewan Kazi Fahima, Paavani Atluri, Kenneth Wasser, Nadeem Baig

(Department of Internal Medicine, Monmouth Medical Center, Long Branch, NJ, USA)

Med Sci Case Rep 2016; 3:32-36

DOI: 10.12659/MSCR.898697


BACKGROUND: IgA vasculitis (IgAV), known as Henoch-Schönlein purpura, is typically seen in children and is usually self-limited. The most common findings are palpable purpura without thrombocytopenia and coagulopathy, arthritis/arthralgia, abdominal pain, and renal disease.
CASE REPORT: We present the case of an adult male with IgA vasculitis presenting with enteritis as an initial presentation, in who initial traditional management failed to improve symptoms.
CONCLUSIONS: Atypical presentations of IgA vasculitis are important to include in the early differential diagnosis of enteritis because steroids, if begun promptly, can have symptomatic improvement and reduce the duration of illness.

This paper has been published under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially.
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