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原发性小肠淋巴管扩张症 被引量:4

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摘要 原发性小肠淋巴管扩张症(primary intestinal lymphangiectasis,PIL)是一种以肠腔内黏膜下淋巴系统扩张,淋巴液向肠腔渗漏为特征的罕见疾病[1],属于蛋白丢失性肠病的一种。临床上以低蛋白血症、腹泻、低淋巴细胞血症为主要表现[2].其中低蛋白血症是其最具特征性的表现。
出处 《中华消化杂志》 CAS CSCD 北大核心 2011年第6期420-421,共2页 Chinese Journal of Digestion
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  • 1邬云红,李秀钧,梁荩忠,杨丽,陈德才.以低蛋白血症为突出表现的原发性小肠淋巴管扩张症[J].中华医学杂志,2004,84(24):2137-2138. 被引量:10
  • 2潘道香,唐久来,吴德,许晓燕,王德农.血清抗肌内膜抗体IgA和IgG水平检测在谷胶病诊断中的意义[J].实用儿科临床杂志,2006,21(17):1168-1169. 被引量:1
  • 3王玉环,黄瑛,梁英杰,邵彩虹.原发性小肠淋巴管扩张症2例并文献复习[J].中国循证儿科杂志,2007,2(6):434-437. 被引量:20
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