Type 6B Choledochal Cyst Unveiled: A Rare Entity in Pediatric Surgery – A Case Report and Review

Choledochal cyst(CDC) originating from the cystic duct (Type VI A) is uncommon. Dilatation of both the common bile duct (CBD) and cystic duct (Type VI B) is exceptionally rare in children, with only a handful of adult cases documented in medical literature to date. We report a case of a 1-year-old child who was diagnosed with a Type VI B CDC involving dilation of both the cystic and CBDs, confirmed by imaging and histopathology following cholecystectomy, cyst excision, and hepaticoduodenostomy. While recent medical literature has begun to explore Type VI CDCs, documented cases, particularly in pediatric patients, remain extremely scarce. This case report contributes to the emerging understanding of Type VI B CDCs, providing valuable insights into their clinical presentation, diagnostic approach, and surgical management outcomes.

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Publication Details

Journal
Journal of Indian Association of Pediatric Surgeons
Published
2025-02-06
DOI
https://doi.org/10.4103/jiaps.jiaps_219_24
Primary Topic
Pediatric Hepatobiliary Diseases and Treatments
Type
article
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article

Type 6B Choledochal Cyst Unveiled: A Rare Entity in Pediatric Surgery – A Case Report and Review

Naveen Kumar, Tarun John K Jacob, B Elisha Raju, Amartya Sen
1 links
Journal of Indian Association of Pediatric Surgeons
Pediatric Hepatobiliary Diseases and Treatments
article

Type 6B Choledochal Cyst Unveiled: A Rare Entity in Pediatric Surgery – A Case Report and Review

Naveen Kumar, Tarun John K Jacob, B Elisha Raju, Amartya Sen
article en

Abstract

Choledochal cyst(CDC) originating from the cystic duct (Type VI A) is uncommon. Dilatation of both the common bile duct (CBD) and cystic duct (Type VI B) is exceptionally rare in children, with only a handful of adult cases documented in medical literature to date. We report a case of a 1-year-old child who was diagnosed with a Type VI B CDC involving dilation of both the cystic and CBDs, confirmed by imaging and histopathology following cholecystectomy, cyst excision, and hepaticoduodenostomy. While recent medical literature has begun to explore Type VI CDCs, documented cases, particularly in pediatric patients, remain extremely scarce. This case report contributes to the emerging understanding of Type VI B CDCs, providing valuable insights into their clinical presentation, diagnostic approach, and surgical management outcomes.

Journal of Indian Association of Pediatric SurgeonsVol. 30(2)
Christian Medical College, Vellore (IN), Christian Medical College (IN)
Good health and well-being
Openalex Percentile: Top 96%
Pediatric Hepatobiliary Diseases and Treatments
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