Intestinal Behçet’s Disease Diagnosed by Capsule Endoscopy

C. Gubler; P. Bauerfeind

doi:10.1055/s-2005-861429

Endoscopy, Table of Contents

Endoscopy 2005; 37(7): 689
DOI: 10.1055/s-2005-861429

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Intestinal Behçet’s Disease Diagnosed by Capsule Endoscopy

C. Gubler¹ , P. Bauerfeind¹

¹ Division of Gastroenterology, Department of Internal Medicine, Universitätsspital Zürich, Zürich, Switzerland

Abstract

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Figure 1 A 24-year-old woman with known Behçet’s disease complained of intermittent cramping abdominal pain. The diagnosis of Behçet’s disease had been based on necrotizing vasculitis at the vulva. The abdominal pain always resolved promptly when steroids were given; no nonsteroidal anti-inflammatory drugs (NSAIDs) were taken. In the middle jejunum, capsule endoscopy revealed pseudopolypoid lesions without villi, as described in enteroclysis studies.

Figure 2 Small aphthoid lesions were found within the terminal ileum. The two distinct lesions seen on capsule endoscopy are indicative of intestinal involvement, namely the mucosal form of Behçet’s disease.

Figures

Figure 1 A 24-year-old woman with known Behçet’s disease complained of intermittent cramping abdominal pain. The diagnosis of Behçet’s disease had been based on necrotizing vasculitis at the vulva. The abdominal pain always resolved promptly when steroids were given; no nonsteroidal anti-inflammatory drugs (NSAIDs) were taken. In the middle jejunum, capsule endoscopy revealed pseudopolypoid lesions without villi, as described in enteroclysis studies.

Figure 2 Small aphthoid lesions were found within the terminal ileum. The two distinct lesions seen on capsule endoscopy are indicative of intestinal involvement, namely the mucosal form of Behçet’s disease.