open access

Vol 63, No 1 (2004)
Original article
Submitted: 2012-02-06
Published online: 2003-12-03
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The cystic artery in human foetuses

Piotr Flisiński, Michał Szpinda, Mariusz Flisiński
Folia Morphol 2004;63(1):47-50.

open access

Vol 63, No 1 (2004)
ORIGINAL ARTICLES
Submitted: 2012-02-06
Published online: 2003-12-03

Abstract

The cystic artery varies in origin, course and number and it is important to recognise it during operative procedure. Insufficient recognition of its anatomical variation may contribute to a dangerous situation, especially during laparoscopic cholecystectomy. To prevent iatrogenic injuries of the vessels and bile ducts, correct preparation with clear identification of the anatomic structures is essential. Special attention must be given to the course of the cystic artery through the hepato-billiary triangle (Calot`s triangle). The assumption of the present study was recognition of the vasculature of the gallbladder in human foetuses. The purpose of this investigation was to determine the origin of the cystic artery and its relation to Calot’s triangle.
In this study the cystic artery was most often (97.06%) a single vessel and only in one case (2.94%) was it a double vessel. It arose most often (82.34%) from the right proper hepatic artery, rarely from its trunk (8.82%) or its left branch (5.88%) and most rarely (2.94%) from the gastroduodenal artery. In all but one case the cystic artery coursed within Calot’s triangle. Its exceptional course out of Calot’s triangle concerned a cystic artery originating from the gastroduodenal artery (2.94%). The cystic artery most frequently (67.66%) runs behind the common hepatic duct, rarely (29.40%) over the common hepatic duct and most rarely (2.94%) on the left side of the cystic duct. In the material examined the cystic artery was not observed running in front of the common hepatic duct. The short type of cystic artery trunk (52.93%) was observed more frequently than the long one (44.13%).

Abstract

The cystic artery varies in origin, course and number and it is important to recognise it during operative procedure. Insufficient recognition of its anatomical variation may contribute to a dangerous situation, especially during laparoscopic cholecystectomy. To prevent iatrogenic injuries of the vessels and bile ducts, correct preparation with clear identification of the anatomic structures is essential. Special attention must be given to the course of the cystic artery through the hepato-billiary triangle (Calot`s triangle). The assumption of the present study was recognition of the vasculature of the gallbladder in human foetuses. The purpose of this investigation was to determine the origin of the cystic artery and its relation to Calot’s triangle.
In this study the cystic artery was most often (97.06%) a single vessel and only in one case (2.94%) was it a double vessel. It arose most often (82.34%) from the right proper hepatic artery, rarely from its trunk (8.82%) or its left branch (5.88%) and most rarely (2.94%) from the gastroduodenal artery. In all but one case the cystic artery coursed within Calot’s triangle. Its exceptional course out of Calot’s triangle concerned a cystic artery originating from the gastroduodenal artery (2.94%). The cystic artery most frequently (67.66%) runs behind the common hepatic duct, rarely (29.40%) over the common hepatic duct and most rarely (2.94%) on the left side of the cystic duct. In the material examined the cystic artery was not observed running in front of the common hepatic duct. The short type of cystic artery trunk (52.93%) was observed more frequently than the long one (44.13%).
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Keywords

hepatoduodenal ligament; Calot’s triangle; cystic artery syndrome

About this article
Title

The cystic artery in human foetuses

Journal

Folia Morphologica

Issue

Vol 63, No 1 (2004)

Article type

Original article

Pages

47-50

Published online

2003-12-03

Page views

634

Article views/downloads

1489

Bibliographic record

Folia Morphol 2004;63(1):47-50.

Keywords

hepatoduodenal ligament
Calot’s triangle
cystic artery syndrome

Authors

Piotr Flisiński
Michał Szpinda
Mariusz Flisiński

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