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A rare disease more common than perceived: Two case studies and brief review of IgA Vasculitis

Journal: International Journal of Dermatology and Clinical Research (Vol.5, No. 1)

Publication Date:

Authors : ; ;

Page : 003-005

Keywords : gA Vasculitis; Incidence; Misdiagnosis; Criterion;

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Abstract

Immunoglobulin A (IgA) Vasculitis, more commonly known as Henoch-Schönlein Purpura (HSP), is a disorder which causes inflammation and bleeding in the small blood vessels of the skin, joints, intestines, and kidneys. We report 2 cases of IgA vasculitis found in a rural emergency department: 1) HSP in an 8-year-old male who was initially misdiagnosed with insect bites 2) HSP in an adult male patient. We present both cases and a literature review, indicating that low incidence may be secondary to under diagnosis, arguing for a need of further education on the subject.

Last modified: 2019-02-11 16:45:44