Related Experiment Video
Updated: May 30, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Meckel syndrome with Caroli disease and choledochal cysts
Sandhya Venkatachala1, Ammu Sivaraman
1Department of Pathology, PSG Institute of Medical Sciences & Research, PSG Hospitals, Peelamedu, Coimbatore, India. sandhyavenkatachala@yahoo.co.in
Abstract:
Meckel syndrome is a lethal autosomal recessive disorder characterized by the triad of cystic renal dysplasia, occipital encephalocele, or other anomaly of the central nervous system and post-axial polydactyly. Malformation of the ductal plate is an integral component of Meckel syndrome. Ductal plate malformations include congenital hepatic fibrosis, biliary hamartoma, autosomal dominant polycystic liver disease, Caroli disease, and choledochal cyst. The occurrence of cystic hepatic disease, Caroli disease, and choledochal cyst have not been highlighted. This is a report of a 26-week fetus with features of Meckel syndrome, Caroli disease, and choledochal cyst.
Related Concept Videos
Esophageal Achalasia
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Cholecystitis
Diverticular Disease of the Colon
Inborn Errors of Metabolism
Pleiotropy