Henoch-Schönlein purpura (HSP) is systemic vasculitis disease with various clinical manifestations. Gastrointestinal symptoms in patients with HSP are usually common, with an incidence rate of 62-90%. Most of these gastrointestinal symptoms occur after typical skin purpura, which is a very important clinical evidence for making a diagnosis of HSP. It is difficult to diagnose HSP without skin rash. About 25% of patients may experience gastrointestinal symptoms as their first symptoms. Herein, we report a case of ileo-colic intussusception associated with HSP in a 5-years-old girl presented with diffuse abdominal distension. Our patient did present any symptoms of HSP, such as purpura, arthralgia or arthritis, before surgery.
CITATION STYLE
Kim, K. Y. (2017). Henoch-Schönlein Purpura Presenting as Intussusception. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi, 69(6), 372–376. https://doi.org/10.4166/kjg.2017.69.6.372
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