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Biliary cast syndrome: literature review and a single centre experience in liver transplant recipients |
Narasimhaiah Srinivasaiah, Mettu Srinivas Reddy, Schlok Balupuri, David Talbot, Bryon Jaques and Derek Manas |
Newcastle-upon-Tyne, UK
Author Affiliations: Department of Hepatobiliary & Transplant Surgery, Freeman Hospital, Freeman Road, High Heaton, Newcastle-upon-Tyne, NE7 7DN, UK (Srinivasaiah N, Reddy MS, Balupuri S, Talbot D, Jaques B and Manas D)
Corresponding Author: Derek Manas, Consultant Hepatobiliary & Transplant Surgeon, Freeman Hospital, Newcastle-upon-Tyne, NE7 7DN, UK (Tel: 0044-191-2336161; Fax: 0044-191-2231191; Email: Derek.manus@nuth.nhs.uk) |
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Abstract BACKGROUND: Biliary cast syndrome (BCS) is an unusual complication of orthotopic liver transplantation (OLTx), and its management is difficult. Limited success using endoscopic retrograde cholangiopancreatography (ERCP) or open exploration to clear casts has been reported, but failure usually results in re-transplantation. We aimed to review our experience with BCS and highlight a novel combined percutaneous and endoscopic approach for duct clearance. A brief review of the literature is given.
METHODS: We retrospectively reviewed our experience of managing BCS using case notes review. Details were also gathered from radiology, where interventional procedures were carried out.
RESULTS: We had a total of three cases of BCS reported between 2002 and 2005. Multiple attempts were made to remove these casts. All three were treated in a variety of ways. Management is discussed along with highlighting a novel combined percutaneous and endoscopic approach for duct clearance.
CONCLUSIONS: BCS is a potential complication of OLTx. Surgical and endoscopic methods of removing casts are used. However, in circumstances where these methods are technically difficult, a percutaneous endoscopic approach with serial dilatation of the cutaneous port and surgical removal of casts can be done.
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