Choledochal cysts (CCs), also known as congenital choledochal dilatations, can be single or multiple and involve the intrahepatic or extrahepatic bile ducts. These cysts are most commonly found in Asia, where the incidence is approximately 100 times higher than in Europe and the United States, affecting about 1 in 1,000 individuals1. CCs are most commonly diagnosed in children2. However, the number of adult patients diagnosed with CCs has increased in recent years, particularly among young females, who are affected at a rate four times higher than males3. The etiology of CCs remains unclear, but it is widely accepted that the cause may be the reflux of pancreatic fluid into the common bile duct, which is caused by anomalous pancreaticobiliary ductal union (APBDU)4,5. CCs in adults do not have specific symptoms and often present with abdominal pain, jaundice, and fever, which are commonly due to the complications of cholangitis. In addition to cholangitis, other complications of CCs include gallstones, pancreatitis, bile duct stones, and cholangiocarcinoma6. Due to the risk of cholangiocarcinoma and other complications, the removal of choledochal cysts (CCs) is recommended2.
The Todani classification is the most commonly used clinical criterion for staging choledochal cysts (CCs). It categorizes CCs into five types, with 80% of adult lesions being type I cysts7. The treatment for type I biliary dilatation has evolved; it initially involved cyst-jejunostomy but has progressed to completely removing the cyst and reconstructing the bile duct. Previously, the treatment for type I choledochal cysts (CCs) was cyst enterostomy. However, this procedure was later found to be associated with long-term complications, including anastomotic stricture, recurrent cholangitis, and malignancy8. Open total cyst removal and biliary reconstruction are now common9 and have become the dominant surgical procedures for the treatment of choledochal cysts10. As a group with high morbidity, younger women demand more cosmetic outcomes from their surgeries, and this demand has led to the increased use of laparoscopy in the treatment of choledochal cysts11. Several studies have shown that laparoscopic CC resection is comparable in efficacy to open surgery but less invasive, perhaps making it a better option for choledochal cysts11,12,13.
This article presents a case of laparoscopic excision of a choledochal cyst (CC, Todani type I) and a Roux-en-Y choledochojejunostomy behind the colon in an adult. It describes the complete procedure of laparoscopic resection of the CC and the choledochal-jejunal Roux-en-Y anastomosis. After dissecting and excising the CC, the gallbladder was removed. Subsequently, the jejunal loop was prepared, and the gastrocolic ligament and transverse mesocolon were incised to create a channel for the jejunal loop. The jejunal loop was then brought up through this channel to the hepatoduodenal ligament for an end-to-side anastomosis with the common bile duct. The mesocolic aperture was subsequently closed. A side-to-side anastomosis of the jejunum was performed approximately 45 cm from the jejunal anastomotic stoma. After cleansing the abdominal cavity and ensuring hemostasis, the operation was concluded. This approach is effective, allows for rapid postoperative recovery, and preserves the anatomical position of the bowel, making it a preferred treatment option for CC (Todani type I).