Idiopathic mesenteric phlebosclerosis (IMP) with sepsis and death: a case study

Xue-Lei Zhou, Xue-mei Wan, Jing Chen, Z. Xie
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Abstract

Idiopathic mesenteric phlebosclerosis (IMP) is a rare clinical manifestation of ischemic enteropathy. There are no specific manifestations in the early stages. Digestive symptoms only present in the advanced stage. Diagnosis relies on extensive calcification of the mesenteric venule and extensive intestinal wall thickening via computed tomography (CT) scanning. A 50 years old Chinese woman who had taken herbal medicine for three years was diagnosed with IMP. All treatment after admission was in vain and she died 30 days thereafter. Therefore, when a patient with long-term oral intake of herbal medicine, which contains geniposde, presents with unknown ischemia, abdominal pain, mucinous stools, bloody stools, attention should be paid to screen IMP. 
特发性肠系膜静脉硬化(IMP)与败血症和死亡:一个案例研究
特发性肠系膜静脉硬化(IMP)是一种罕见的缺血性肠病临床表现。早期没有特别的表现。消化系统症状只有在晚期才会出现诊断依赖于肠系膜小静脉的广泛钙化和广泛的肠壁增厚。一位50岁的中国妇女,服用中药3年,被诊断为IMP,入院后所有治疗无效,30天后死亡。因此,当患者长期口服含有geniposde的中草药,出现不明原因的缺血、腹痛、粘液性便、血便时,应注意筛查IMP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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