Literature DB >> 11555112

Repeated intestinal perforation caused by an incomplete form of Behçet's syndrome.

F H Ng1, T C Cheung, K C Chow, S Y Wong, W F Ng, H C Chan, W K Chau, C M Chang.   

Abstract

Behçet's disease, as initially described, is a triad of recurrent oral and genital ulcers and relapsing uveitis. The incomplete form, in which there is no ocular involvement, has been described in Japan and Korea, but this is not commonly recognized in the southern Chinese. We reported herein a rare case of repeated intestinal perforations caused by an incomplete form of Behçet's syndrome in a southern Chinese man.

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Year:  2001        PMID: 11555112     DOI: 10.1046/j.1440-1746.2001.02423.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  1 in total

1.  Pathologic Features of Behçet's Disease in the Tubuler Gut.

Authors:  Tuba Kara; Duygu Düşmez Apa
Journal:  Patholog Res Int       Date:  2011-11-15
  1 in total

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