Current status of the biliary tract malformation

doi:10.5409/wjcp.v13.i2.91268

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Jun 9, 2024 (publication date) through Jul 21, 2024

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World Journal of Clinical Pediatrics

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2219-2808

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Pediatr. Jun 9, 2024; 13(2): 91268
Published online Jun 9, 2024. doi: 10.5409/wjcp.v13.i2.91268

Current status of the biliary tract malformation

Krishna Kumar Govindarajan

Krishna Kumar Govindarajan, Department of Pediatric Surgery, JIPMER, Pondicherry, Pondicherry 605006, India

Author contributions: Govindarajan KK was responsible for conception, compilation and submission.

Conflict-of-interest statement: No conflict of interest declared.

Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

Corresponding author: Krishna Kumar Govindarajan, FACS, MBBS, MCh, MNAMS, MS, Professor, Department of Pediatric Surgery, JIPMER, Pondicherry, Dhanvantri Nagar, Pondicherry 605006, India. sasisang@rediffmail.com

Received: December 26, 2023
Revised: April 13, 2024
Accepted: April 18, 2024
Published online: June 9, 2024
Processing time: 164 Days and 10.1 Hours

Core Tip

Core Tip: The biliary tract malformation has undergone a metamorphosis from its previous nomenclature of choledochal cyst owing to a variety of reasons. The etiology, embryopathology and the current classification require revisiting due to the same. The review looks at the same in detail.