Case Report
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World J Gastroenterol. Apr 14, 2014; 20(14): 4110-4114
Published online Apr 14, 2014. doi: 10.3748/wjg.v20.i14.4110
Prolonged small vessel vasculitis with colon mucosal inflammation as first manifestations of Behçet’s disease
Xiao-Ning Yang, Zhen-Shi Ye, Yan-Yun Fan, Yi-Qun Hu
Xiao-Ning Yang, Zhen-Shi Ye, Yan-Yun Fan, Yi-Qun Hu, Department of Gastroenterology, Zhongshan Hospital Xiamen University, Xiamen 361004, Fujian Province, China
Author contributions: Hu YQ designed the report and was the attending doctor for the patient; Ye ZS and Fan YY performed diagnostic imaging diagnosis and organized the report; and Yang XN wrote the paper.
Supported by Major Foundation of Xiamen Gastroenterology Center, No. 200702
Correspondence to: Yi-Qun Hu, MD, Department of Gastroenterology, Zhongshan Hospital Xiamen University, 201 Hubin South Road, Xiamen 361004, Fujian Province, China. hyq0826@yahoo.com
Telephone: +86-592-2590151  Fax: +86-592-2590150
Received: September 10, 2013
Revised: December 25, 2013
Accepted: January 20, 2014
Published online: April 14, 2014
Processing time: 215 Days and 20.7 Hours
Abstract

Behçet’s disease is a chronic, relapsing, systemic vasculitis of unknown aetiology. Patients present manifestations of gastrointestinal complications, including mouth lesions, small and large intestinal lesions, and vascular lesions in the abdomen. In some cases, the intestinal ulcers of patients with Behçet’s disease are indistinguishable from those of Crohn’s disease, tuberculosis, vasculitis and other diseases. In this article, we present a case of atypical Behçet’s disease with a complicated medical history and multisystem damage, for the purpose of better management of this disease.

Keywords: Behçet’s disease; Vasculitis; Intestinal ulcers

Core tip: Behçet’s disease is systemic inflammatory vasculitis of unknown aetiology. Its clinical manifestation of gastrointestinal complications varies greatly. Diagnosis is mainly based on typical clinical findings: no specific serum markers or pathological features are available. However, in clinical practice, it is often challenging to make a prompt and correct diagnosis when gastroenteropathy is presented as the initial or predominant manifestation in Behçet’s disease patients. The disease is sometimes misdiagnosed as inflammatory bowel disease or other disorders. We present a case of atypical Behçet’s disease with a complicated medical history and multisystem damage, for the purpose of better management of this disease.