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JOURNAL ARTICLE
Late-onset IgA vasculitis in adult patients exhibits distinct clinical characteristics and outcomes.
Seokchan Hong, Soo Min Ahn, Doo-Ho Lim, Byeongzu Ghang, Won Seok Yang, Sang Koo Lee, Yong-Gil Kim, Chang-Keun Lee, Bin Yoo
OBJECTIVES: The aim of this study was to determine whether adult IgA vasculitis patients who developed the disease at an older age differ from early-onset patients in terms of clinical features and outcomes. METHODS: All consecutive adult patients who were diagnosed with IgA vasculitis between January 1997 and December 2014 were reviewed retrospectively. Patients who developed the disease at an older age (≥60 years; late-onset) were compared with those with an earlier onset of disease (<60 years; early-onset)...
May 2016: Clinical and Experimental Rheumatology
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JOURNAL ARTICLE
Charles B Chen, Srikanth Garlapati, Jeffrey D Lancaster, Zachary Zinn, Patrick Bacaj, Kamakshya P Patra
Henoch-Schönlein purpura (HSP) is a systemic vasculitis that is common in the pediatric population and often presents with the classical triad of palpable purpura, arthralgia, and abdominal pain. We describe a case of HSP in a 14-year-old adolescent girl who presented with atypical features of painful hemorrhagic bullae. The patient was treated with high-dose steroids, dapsone, and supportive therapy with remarkable improvement.
October 2015: Cutis; Cutaneous Medicine for the Practitioner
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