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Hypersensitivity Angitis with Intestinal Involvements, Report of a Case Yukiya Yoshida 1 , Mitsuyo Hashimoto 1 , Kazuo Hayakawa 1 , Miki Adachi 4,5 , Tetsuichiro Muto 6 1Department of Gastroenterology, Toranomon Hospital 4Department of Pathology, Toranomon Hospital 6The First Department of Surgery, Faculty of Medicine, University of Tokyo Keyword: 炎症性腸疾患 , 過敏性血管炎 , 壊死性血管炎 pp.723-730
Published Date 1990/6/25
DOI https://doi.org/10.11477/mf.1403110969
  • Abstract
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 A 27-year-old male was admitted to our hospital because of fever, diarrhea, arthralgia and eruption. Radiologic and endoscopic examinations showed multiple discrete ulcers in the left side colon, several aphthoid ulcers in the right side colon and longitudinal ulcers with fissure in the terminal ileum, mainly along the mesenteric attachment. Crohn's disease was suspected from these findings. However, clinical course and histological findings as follows were not typical for Crohn's disease. First, ulcers healed in only 4 weeks after steroid administration was started. Second, although relapse and remission were repeated four times, deformity of the intestinal tract was mild. Third, relapse occurred without causing symptoms of intestinal tract. Finally, epithelioid cell granuloma was not found histologically. Biopsy specimen obtained from eruption, revealing necrotizing angitis in the arterioles, gave us a clue to the correct diagnosis in this case. Thus, clinical findings and course in this case represent intestinal involvement in hypersensitivity angitis.


Copyright © 1990, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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