Volume 57, Issue 3 pp. 498-500
Brief Report

Management of intestinal bleeding with single-dose cyclophosphamide in Henoch–Schönlein purpura

Ünal Uluca

Corresponding Author

Ünal Uluca

Departments of Pediatrics

Correspondence: Ünal Uluca, MD, Department of Pediatrics, Dicle University Medical School, Diyarbakır, Turkey. Email: [email protected]Search for more papers by this author
Aydın Ece

Aydın Ece

Departments of Pediatric Rheumatology, Dicley University Medical School, Diyarbakir, Turkey

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Velat Şen

Velat Şen

Departments of Pediatrics

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Servet Yel

Servet Yel

Departments of Pediatrics

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İlhan Tan

İlhan Tan

Departments of Pediatrics

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Duran Karabel

Duran Karabel

Departments of Pediatrics

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First published: 26 June 2015
Citations: 13

Abstract

In these case series, we report on six children (3 girls, 3 boys) aged 5–13 years with Henoch–Schönlein purpura (HSP) who developed severe gastrointestinal (GI) bleeding resistant to both 2 mg/kg or pulse (10–30 mg/kg) i.v. methylprednisolone. All patients responded to single-dose (500 mg/m2) i.v. cyclophosphamide (CPA) and none of them developed new GI bleeding after CPA treatment. No patients required surgical intervention. Single high-dose CPA may be beneficial in HSP with severe GI involvement, in which bleeding is non-responsive to high-dose steroids.

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