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Choledochal Cysts: Evaluation and Management

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ERCP and EUS

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Abstract

Choledochal cysts are rare congenital dilations of the biliary tree. Most are diagnosed in infancy or childhood, though the incidence of adult diagnosis is increasing. Early recognition and appropriate treatment are important due to risk of malignant transformation. Endoscopic retrograde cholangiopancreatography (ERCP) has a central role in diagnosis, surveillance, and even definitive therapy in a subtype of cysts. This chapter will review the presentation and diagnosis of choledochal cysts as well as their clinical classification and management.

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  1. Department of Gastroenterology and Hepatology, School of Medicine, Huntsman Cancer Center, University of Utah, 30N 1900E 4R118, Salt Lake City, UT 84132, USA

    James Stayner MD & Assoc. Prof. Douglas G. Adler MD, FACG, AGAF, FASGE

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  1. Gastroenterology, Hepatology, and Endoscopy, Brigham and Women’s Hospital, Boston, Massachusetts, USA

    Linda S. Lee

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Stayner, J., Adler, D. (2015). Choledochal Cysts: Evaluation and Management. In: Lee, L. (eds) ERCP and EUS. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2320-5_10

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