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胆道畸形

Biliary tract malformations.

作者信息

Knisely A S

机构信息

Institute of Liver Studies, King's College Hospital, Denmark Hill, London, United Kingdom.

出版信息

Am J Med Genet A. 2003 Nov 1;122A(4):343-50. doi: 10.1002/ajmg.a.20479.

Abstract

The biliary tree extends from the canals of Hering at the margin of the most peripheral portal tracts to the ampulla of Vater. Malformations occur at every level of this structure. Phenotypic features dominate present understanding of these malformations and of the disorders with which they are associated. Classifications of disease will likely shift from a phenotypic basis to a genotypic basis as genes implicated in biliary tree development and function are identified. Involvement of such genes in biliary tree disorders now considered inflammatory, such as extrahepatic biliary atresia, awaits study. The concept of "feeble cholangiocytes" postnatally susceptible to the effects of "toxic bile" is presented.

摘要

胆管系统从最外周门静脉周围区域边缘的赫林管延伸至 Vater 壶腹。该结构的各个层面均可出现畸形。表型特征主导着目前对这些畸形及其相关疾病的认识。随着与胆管系统发育和功能相关的基因被确定,疾病分类可能会从基于表型转向基于基因型。此类基因在目前被认为是炎症性的胆管系统疾病(如肝外胆管闭锁)中的作用尚待研究。文中提出了“脆弱胆管细胞”在出生后易受“毒性胆汁”影响的概念。

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