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Vol. 11. Issue 1.
Pages 150-151 (January - February 2012)
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Vol. 11. Issue 1.
Pages 150-151 (January - February 2012)
Open Access
Unusual cause of common bile duct dilatation in asymptomatic elderly patient: right hepatic artery syndrome
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Adnan Tas
,
Corresponding author
dradnantas@gmail.com

Correspondence and reprint request:
, Seyfettin Koklu**
* Research Fellow, Department of Gastroenterology, Ankara Education and Research Hospital, Ankara, Turkey
** Associate professor, Department of Gastroenterology, Ankara Education and Research Hospital, Ankara, Turkey
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Obstructive jaundice by vascular compression is extremely rare. Luttwak and Schwartz first described jaundice due to an obstruction of the common hepatic duct by an aberrant artery.1 Compression of extrahepatic bile duct (EBD) by right hepatic artery was defined as right hepatic artery syndrome. We present here a rare case of asymptomatic biliary obstruction due to compression of the common bile duct by right hepatic artery.

A 74-year-old female presented with slight epigastric pain. Her past medical history and physical examination were unremarkable. On laboratory examination, alkaline phosphatase, gamma-glutamyl transpeptidase, total biluribin, aspartate amino-transferase and alanine aminotransferase were normal. Ultrasonography revealed moderate dilatation of common bile duct and intrahepatic ducts. Abdominal computerized tomography (CT) showed compression from the dorsum and stenosis of the EBD by the right hepatic artery, but did not reveal a mass or lymph node swelling around EBD. Proximal and distal choleduct was 9.7 mm and 6.8 mm, respectively (Figures 1A, 1B). MRCP showed a stenotic lesion at the level of the upper common hepatic duct. Hepatic artery was normal at CT angiography. Since she was asymptomatic, we decided on regularly follow-up in the out-patient.

Figure 1.

A and B. Abdominal computerized tomography (CT): compression of the extrahepatic bile duct by the right hepatic artery.

(0.12MB).

Compression of the EBD by the right hepatic artery has been reported as a right hepatic artery syndrome. Anatomic variations of biliary tract are found frequently. Among these variations, some reports have described anatomically variable vasculature of the hepatic artery.2 Koops represented that the finding of 604 selective angiographies showed normal anatomy of the hepatic artery in 79.1% and the anomalous arterial patterns in the remaining.3

Because of previous cases were symptomatic, almost all were operated.4,5 Our case was asymptomatic, hence we advice to regular follow-up as out-patient.

In conclusion, arterial compression should be among the differential diagnosis of extrahepatic biliary obstruction.

Disclosure of Interest

There is no financial support.

There is no conflict of interests among the authors.

References
[1.]
Luttwak E.M., Schwartz A..
Jaundice due to obstruction of the common duct by aberrant artery: demonstration of celiac anomaly by translumbar aortography and simultaneous choledochogram.
[2.]
Covey A.M., Brody L.A., Maluccio M.A., Getrajdman G.I., Brown K.T..
Variant hepatic arterial anatomy revisited: digital subtraction angiography performed in 600 patients.
Radiology, 224 (2002), pp. 542-547
[3.]
Koops A., Wojciechowski B., Broering D.C., Adam G., Krupski-Berdien G..
Anatomic variations of the hepatic arteries in 604 selective celiac and superior mesenteric angiographies.
Surg Radiol Anat, 26 (2004), pp. 239-244
[4.]
Miyashita K., Shiraki K., Ito T..
The right hepatic artery syndrome.
World J Gastroenterol, 11 (2005), pp. 3008-3009
[5.]
Baek Y.H., Choi S.R., Lee J.H..
Obstructive jaundice due to compression of the common bile duct by right hepatic artery originated from gastroduodenal artery.
Korean J Gastroenterol, 52 (2008), pp. 394-398
Copyright © 2012. Fundación Clínica Médica Sur, A.C.
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