scholarly journals A Case of Henoch-Schönlein Purpura with Fulminant Complications and Its Long-term Outcome

2019 ◽  
Vol 23 (2) ◽  
pp. 128-133
Author(s):  
Dong Hyun Lee ◽  
Eun-So LEE ◽  
Jeong Hong ◽  
Kwang-Hwa Park ◽  
Ki Soo Pai
2008 ◽  
Vol 23 (9) ◽  
pp. 3010-3016 ◽  
Author(s):  
G. Moroni ◽  
B. Gallelli ◽  
A. Diana ◽  
A. Carminati ◽  
G. Banfi ◽  
...  

2011 ◽  
Vol 6 (8) ◽  
pp. 2034-2040 ◽  
Author(s):  
Joyce P. Samuel ◽  
Cynthia S. Bell ◽  
Donald A. Molony ◽  
Michael C. Braun

2020 ◽  
Vol 82 (6) ◽  
pp. 1393-1399 ◽  
Author(s):  
Emily Baumrin ◽  
Soraya Azzawi ◽  
Jessica St. John ◽  
Mai P. Hoang ◽  
Steven Chen ◽  
...  

2007 ◽  
Vol 22 (10) ◽  
pp. 1717-1722 ◽  
Author(s):  
Mohan Shenoy ◽  
Mark G. Bradbury ◽  
Malcolm A. Lewis ◽  
Nicholas J. A. Webb

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Donghwan Yun ◽  
Dong Ki Kim ◽  
Kook-Hwan Oh ◽  
Kwon Wook Joo ◽  
Kyung Chul Moon ◽  
...  

Author(s):  
William Ray Cassidy ◽  
Ketut Suryana ◽  
Dewi Catur Wulandari

Henoch-Schönlein purpura (HSP), also known as immunoglobulin A vasculitis, is a self-limiting, small vessel systemic vasculitis rarely found in adults characterized by palpable purpura, arthritis or arthralgia, gastrointestinal, and renal involvement. We report a case of a 31-year-old male with HSP complicated with severe gastrointestinal manifestations mimicking acute abdomen. He was successfully managed with conservative approach. Meticulous diagnosis, treatment, and long-term monitoring are important to reduce patient morbidity.


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