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Idiopathic Mesenteric Phlebosclerosis after a 3-Year Period of Observation, Report of an Autopsy Case Masaki Yoshida 1 1Department of Internal Medicine, Tounou Kousei General Hospital, Mizunami, Japan Keyword: 特発性腸間膜静脈硬化症 , 静脈硬化性大腸炎 , 剖検 , 経過観察 pp.248-257
Published Date 2009/2/25
DOI https://doi.org/10.11477/mf.1403101587
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 Idiopathic mesenteric phlebosclerosis is a recently discovered, rare and new disease entity causing chronic ischemic colitis. 208 cases of this disease have been reported since 1991. Japanese cases numbered 199, Taiwanese cases numbered 8 and there was only one Chinese case. However, this disease has not been reported among other races. This is a first autopsy case after a 3- year period of observation. A 72- year-old woman visited our hospital because of lower abdominal fullness and slight diarrhea. Barium enema showed the disappearance of semilunar folds and the thumbprinting appearance of the ascending colon and transverse colon. On the other hand, almost normal findings were obtained in the left hemicolon. Colonoscopic examination showed dark purple and edematous mucosa with loss of the normal vascular pattern in the ascending colon and transverse colon. In the sigmoid colon, colonoscopic examination showed only dark purple mucosa without mucosal edema and disappearance of semilunar folds. Abdominal CT showed bowel wall thickening with intramural calcifications in the cecum, ascending colon and transverse colon. 3DCT showed calcifications around the right hemicolon. After 3 years, calcifications around the colon and along the mesentery markedly increased and extended to the left hemicolon. The patient suddenly died because of severe aspiration pneumonia. An autopsy was carried out. Macroscopic findings of the resected specimen showed dark purple thickened ascending colon and transverse colon. Ileum and appendix were normal. A radiograph of the resected colon showed tortuous threadlike calcifications within the cecum, ascending colon, transverse colon and descending colon. These calcifications predominantly affected the right hemicolon. Microscopic examination showed marked fibrous thickening of the submucosal layer. The veins in the colonic wall showed tortuous appearance. Marked fibrous thickening of the venous walls with calcification, ossification and recanalization showed severe luminal narrowing. Perivascular fibrosis of the intramural colonic veins was also found. These findings were consistent with mesenteric phlebosclerosis.


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

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