A choledochal cyst is a congenital dilation or swelling of the bile ducts (the tubes that carry bile from the liver to the duodenum). These cysts cause bile stasis, which can lead to stone formation, recurrent liver infections, pancreatitis, and long-term risk of bile duct cancer if left untreated.
Choledochal cysts are congenital and are widely believed to be caused by:
Symptoms can appear at any age, from infancy to adulthood:
A choledochal cyst can lead to recurrent episodes of cholangitis, pancreatitis, and progressive liver damage if left untreated. More importantly, there is a significant risk of malignant transformation (cancer) within the cyst wall as the child grows older. Complete surgical excision at a young age eliminates these risks and allows for normal biliary function to be restored.
We utilize the most advanced diagnostic imaging, including MRCP, to precisely map the biliary anatomy before surgery. Post-operatively, our focus is on ensuring smooth recovery and long-term follow-up to monitor liver function. We prioritize minimally invasive techniques to reduce pain and scarring, allowing your child to return to their normal activities quickly.
Complete surgical removal of the choledochal cyst to eliminate the risk of recurrent infections and malignancy.
Reconstruction of the biliary tract by connecting the remaining healthy bile duct directly to the small intestine.
Utilizing laparoscopic or robotic-assisted techniques for precision, faster recovery, and minimal scarring.
High-resolution Ultrasound and MRCP (MRI of the bile ducts) are used to map the exact anatomy of the cyst and plan the reconstruction.
The entire dilated duct is precisely removed. We prioritize minimally invasive techniques to reduce pain and visible scarring.
The liver's bile duct is connected to the small intestine (Roux-en-Y), restoring normal digestion and preventing future complications.
"Our daughter had recurrent abdominal pain that no one could figure out. Dr. Chowdhary diagnosed a choledochal cyst and performed a brilliant laparoscopic surgery."
"Expert hands! The complex reconstruction was done so precisely. Our son was back to his normal self within two weeks. We are so grateful."
"We were worried about the long-term cancer risk. Dr. Sujit's clarity and skill gave us peace of mind. The scars are almost invisible today."
"The precision in Dr. Chowdhary's minimally invasive surgery is incredible. His confidence gave us immense peace of mind."
"We traveled from another city just for Dr. Chowdhary. His approach is very scientific and methodical yet very caring."
"The nursing staff and Dr. Sujit are a fantastic team. They handled our child's surgery with so much care and warmth."
"The best decision we made for our child's health. Dr. Chowdhary is incredibly patient and explained everything so well."
Choledochal cyst surgery is one of the most complex reconstructions in pediatric surgery. Expertise in biliary anatomy and suturing is paramount.
It is a congenital cystic dilation of the bile ducts that can cause bile stasis, jaundice, liver damage, or infection.
Removal is essential to prevent complications such as recurrent cholangitis, pancreatitis, stone formation, and long-term risk of malignancy.
It involves complete excision of the cyst followed by reconstruction of the biliary pathway, usually connecting the liver duct to the small intestine (Hepaticojejunostomy).
Yes, laparoscopic or robotic-assisted excision of choledochal cysts is now the standard approach, offering excellent visualization and quicker recovery.
Abdominal pain, jaundice, and a palpable abdominal mass are the classic symptoms.
Children stay in the hospital for 4 to 6 days after surgery and return to normal activity within 2 to 3 weeks.
Once fully recovered, children can typically enjoy a normal, healthy diet without any lifelong restrictions.
Complete cyst excision prevents long-term liver and biliary complications. Schedule a consultation today.
D6, Club, 2, opposite Vasant Vihar, Vasant Vihar, New Delhi, Delhi 110057
+91 98732 06761
