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Phlebosclerotic Colitis, Report of a Case Hidehiro Kawabata 1 , Ikuo Takase 1 , Akitoshi Murata 1 , Takuya Watanabe 1 , Youichi Ajioka 2 , Hidenobu Watanabe 3 1Division of Gastroenterology, Labour Welfare Corporation Niigata Rosai Hospital 2Division of Molecular and Functional Pathology, Department of Cellular Function, Graduate School of Medical and Dental Sciences, Course of Molecular and Cellular Medicine, Niigata University 3Division of Molecular and Diagnostic Pathology, Graduate School of Medical and Dental Sciences, Course of Molecular and Cellular Medicine, Niigata University Keyword: 静脈硬化症 , 虚血性病変 , 石灰化 , 若年発症 pp.1468-1476
Published Date 2003/9/25
DOI https://doi.org/10.11477/mf.1403100765
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 A 28-year-old man presented with right abdominal pain during the 4 months before his admission to the Labour Welfare Corporation Niigata Rosai Hospital. Abdominal conventional radiography showed a linear calcification of the vascular wall of the ascending colon. Barium enema examination showed a thumb-printing sign, sclerosis of the colonic wall and luminal narrowing of the ascending colon and transverse colon. Colonoscopic examination demonstrated dark blue mucosa, luminal narrowing and several small ulcers. Abdominal computed tomography revealed the thickening of the colonic wall and marked linear calcification of the vascular wall of the ascending colon and transverse colon. Based on these findings, the patient was diagnosed as having phlebosclerotic colitis. Phlebosclerotic colitis has rarely been reported. We discuss the clinical characteristics of this case.


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

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