Stomach and Intestine(Tokyo) Volume 14, Issue 6 (June 1979)
Japanese

Intestinal Behçet with Multiple Ileal Ulcers; A case report H. Tazawa 1 , Y. Wakabayashi 1 , M. Haraikawa 1 , T. Shinozuka 1 , S. Mayama 1 , G. Hayashi 1 , A. Kariya 1 , H. Ohkubo 2 , M. Nishizawa 3 1Division of Diagnostic Radiology, Chiba Cancer Center Hospital 2Funabashi Central Hospital 3Tokyo Metropolitan Cancer Detection Center pp.807-810
Published Date 1979/6/25
DOI https://doi.org/10.11477/mf.1403107700
  • Abstract
  • Look Inside

 A 38-year-old female had been treated as Behçet syndrome having such typical symptoms as stomatitis, genital ulceration, uveitis and erythema rodosum. Six years later, she had small bowel follow-through study because of abdominal pain, and it revealed three large, irregular-shaped and undermining ulcers at the terminal ileum.

 This patient was diagnosed as complete type of Behçet syndrome, therefore, this type of ulcers in this case was thought to be typical in intestinal Behçet. General characteristics of the ileal ulcers in intestinal Behçet were discussed. Abdominal symptoms are, in the frequent order, lower abdominal pain, diarrhea and ileo-cecal tumor. The most frequently affected site is an ileo-cecal region. The ulcers are usually multiple, and tend to undermine macroscopically. Histology of the ulcers reveals only non-specific inflammatory changes and shows perforative or penetrative findings at the muscular layer of the intestine. The base of the ulcer shows rich in vascularity and round cell infiltration. As an unusal morphological feature in this case, a fistula-like formation within the marginal wall of the ulcer was found. Further observation is needed to determine whether this fistula-like structure is characteristic in intestinal Behçet or not.


Copyright © 1979, Igaku-Shoin Ltd. All rights reserved.

基本情報

05362180.14.6.jpg
胃と腸
14巻6号 (1979年6月)
電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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