Classification of choledochal malformations
نویسنده
چکیده
816 November 2014, Vol. 104, No. 11 Choledochal malformations (CMs) may be characterised by inherent dilatation of the biliary tree without evidence of mechanical obstruction. Dilatation varies from florid and cystic to subtle and fusiform, and was first recognised during postmortem dissection by the German anatomist Abraham Vater, who reported his findings in his 1723 thesis.[1] The objective of this article is to offer a clinically orientated review and identify and discuss areas of controversy in detail.
منابع مشابه
Understanding choledochal malformation.
Choledochal malformations (also known as choledochal cysts) may be characterised as an abnormal dilatation of the biliary tract, in the absence of any acute obstruction. Most appear to be of congenital origin probably related to distal bile duct stenosis, and almost 15% can now be detected antenatally. Excision and biliary reconstruction using a Roux loop as an open operation is still the stand...
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تاریخ انتشار 2014