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Thrombosis warning in children suffering from henoch-schonlein purpura
Luan Li1, Jingwen Zhang, Yunying Zhang
1Department of Dermatology and Venereology, First Affiliated Hospital, Dalian Medical University, Dalian, China.
Insights
Henoch-Schonlein Purpura (HSP), a common childhood vasculitis, can rarely lead to thrombosis. This case highlights the importance of monitoring high-risk children with HSP for this serious complication.
Area of Science:
- Pediatric Rheumatology
- Pediatric Vasculitis
- Pediatric Thrombosis
Background:
- Henoch-Schonlein Purpura (HSP) is the most prevalent form of childhood vasculitis.
- Clinical features typically include purpura, arthritis, abdominal pain, and renal involvement.
- Thrombosis is a recognized, albeit rare, complication of HSP.
Purpose of the Study:
- To report a case of a 14-year-old boy with HSP and suspected superior mesenteric vein thrombosis.
- To review existing literature on HSP-associated thrombosis.
- To emphasize the need for vigilant monitoring of at-risk pediatric patients with HSP.
Main Methods:
- Case presentation of a pediatric patient diagnosed with HSP and superior mesenteric vein thrombosis.
- Comprehensive literature review of reported cases of thrombosis in Henoch-Schonlein Purpura.
- Analysis of potential risk factors contributing to thrombosis in HSP patients.
Main Results:
- The study identified one case of a 14-year-old boy with HSP and superior mesenteric vein thrombosis.
- A review of the literature revealed eight previously reported similar cases.
- The findings indicate a link between HSP and an increased risk of thrombosis.
Conclusions:
- Henoch-Schonlein Purpura is associated with an increased risk of thrombosis.
- Certain risk factors may predispose HSP patients to developing thrombosis.
- Close monitoring of pediatric patients with HSP, particularly those at higher risk, is recommended to detect and manage thrombosis.
Abstract:
Henoch-Schonlein Purpura (HSP) is one of the most common types of vasculitis in children. The characteristic clinical manifestations include non-thrombocytopenic purpura, arthritis or arthralgia, abdominal pain, gastrointestinal hemorrhage and renal abnormalities. Thrombosis has been reported as, a rare complication of HSP. We present the case of a 14-year-old boy who was diagnosed with HSP and suspected superior mesenteric vein thrombosis. We reviewed the relevant literature and found eight similar reported cases. HSP is associated with thrombosis and HSP itself and some risk factors may result in thrombosis. We suggest that physicians should monitor patients with HSP who are at a higher risk of developing thrombosis more closely.
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