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EXPERIENCE & REASON:
Daniel L. Preud'Homme, Sonia Michail, Cathy Hodges, Tonya Milliken, and Adam G. Mezoff
Use of Wireless Capsule Endoscopy in the Management of Severe Henoch-Schonlein Purpura
Pediatrics 2006; 118: e904-e906 [Abstract] [Full text] [PDF]
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[Read eLetters] Is capsule endoscopy necessary in the evaluation of gastrointestinal Henoch-Schonlein vasculitis?
Jae Il Shin, Jae Seung Lee   (23 August 2006)

Is capsule endoscopy necessary in the evaluation of gastrointestinal Henoch-Schonlein vasculitis? 23 August 2006
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Jae Il Shin,
Pediatrician
Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea,
Jae Seung Lee

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Re: Is capsule endoscopy necessary in the evaluation of gastrointestinal Henoch-Schonlein vasculitis?

pedshin2000{at}yahoo.co.kr Jae Il Shin, et al.

Dear Editor, We read with interest an article on ˇ°Use of Wireless Capsule Endoscopy in the Management of Severe Henoch-Schonlein Purpuraˇ± by Preud'homme et al. [1]. They reported a 12-year-old boy with chronic HSP vasculitis, which primarily affects the gastrointestinal tract, showing protracted course, multiple recurrences of hematochezia or melena, and steroid dependency. In this case, wireless capsule endoscopy (WCE) was helpful in evaluating and directing treatment options, such as intensive immunosuppression (cyclophosphamide and MMF). WCE can be used to evaluate morphologically the extent of gastrointestinal vasculitic processs, but it may not give us the information about the severity of gastrointestinal symptoms. There have been some reports describing that severe gastrointestinal symptoms are closely associated with decreased factor XIII levels in both children and adults with HSP [2, 3]. Fukui et al reported that decrease in factor XIII level was correlated with the severity score of clinical symptoms, particularly abdominal symptoms in fifty-six children with HSP, and severe abdominal symptoms were improved remarkably in accordance with the increase of factor XIII level after the administration of factor XIII concentrate compared with non-treated group [2]. Also, Shimomura et al. recently reported an adult patient with HSP who had arthralgia, severe abdominal pain, and low plasma factor XIII activity [3]. In this case, severe abdominal pain was markedly improved immediately after the administration of factor XIII concentrate, suggesting factor XIII activity might play an important role in the pathogenesis of abdominal vasculitic process associated with HSP.

Therefore, it would be helpful to measure factor XIII activity rather than WCE when we assess the severity of mesenteric vasculitis in patients with HSP, and factor XIII concentrate could be useful for alleviating severe abdominal symptoms before considering intensive immunosuppression in HSP patients.

References 1. Preud'homme DL, Michail S, Hodges C, Milliken T, Mezoff AG. Use of Wireless Capsule Endoscopy in the Management of Severe Henoch-Schonlein Purpura. Pediatrics 2006 Jul 31; [Epub ahead of print] 2. Fukui H, Kamitsuji H, Nagao T, et al. Clinical evaluation of a pasteurized factor XIII concentrate administration in Henoch-Schonlein purpura. Japanese Pediatric Group. Thromb Res 1989;56:667-75. 3. Shimomura N, Kawai K, Watanabe S, et al. Adult Henoch-Schonlein purpura with severe abdominal pain treated with dapsone and factor XIII concentrate. J Dermatol 2005;32:124-7.

Conflict of Interest:

None declared