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新生儿胆汁淤积综合征的发病机制(作者译)

[Pathogenesis of the neonatal cholestasis syndrome (author's transl)].

作者信息

Feist D

出版信息

Leber Magen Darm. 1979 Apr;9(2):43-6.

PMID:449570
Abstract

Cholestasis means reduced flow of bile between hepatocytes and duodenum. Functional as well as mechanical factors may be important in the pathogenesis of cholestatic syndromes. Extra- and intrahepatic cholestasis can be distinguished. Intrahepatic bile ducts use to be dilated in extrahepatic cholestasis after early infancy; they are however not dilated in obstructive jaundice of the newborn. Neonatal cholestatic syndromes caused by liver cell diseases may in addition cause an obstruction of extrahepatic bile ducts. At the present time most workers in the field do believe that extrahepatic cholestasis in the newborn is rather due to inflammation than to congenital malformation.

摘要

胆汁淤积是指肝细胞与十二指肠之间胆汁流动减少。功能因素和机械因素在胆汁淤积综合征的发病机制中可能都很重要。肝外和肝内胆汁淤积是可以区分的。在婴儿早期之后,肝外胆汁淤积时肝内胆管通常会扩张;然而,在新生儿梗阻性黄疸中肝内胆管并不扩张。由肝细胞疾病引起的新生儿胆汁淤积综合征还可能导致肝外胆管梗阻。目前,该领域的大多数研究人员确实认为,新生儿肝外胆汁淤积更多是由炎症引起的,而非先天性畸形。

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