Congenital bile duct ectasia is a relatively rare disease of the biliary system, also known as congenital bile duct cyst. The disorder usually develops in childhood, but it can also develop in adulthood. Congenital bile duct dilation can lead to poor bile flow, causing symptoms such as pain, jaundice, and in severe cases, liver failure.
Congenital bile duct dilation** may include a variety of factors such as genetics, environment, etc. This condition usually requires surgery** to restore the normal function of the biliary system. Surgical methods include cyst resection, hepatic canal and jejunal anastomosis, etc.
In the case of congenital bile duct dilation, the following points need to be noted:
1.Timely diagnosis and**: Once congenital bile duct dilation is found, you should seek medical attention as soon as possible for diagnosis and ** to avoid aggravation of the condition and life-threatening.
2.Surgery**: For congenital bile duct dilation, surgery is the main** method. The goal of surgery is to remove the cyst and restore the normal function of the biliary system.
3.Post-operative care: After the operation, it is necessary to closely observe the patient's vital signs, pay attention to dietary adjustment, and avoid complications such as infection.
4.Prevention**: Regular follow-up examinations are required after surgery to detect and deal with possible **conditions in a timely manner.
In conclusion, congenital bile duct ectasia is a relatively serious disease of the biliary system, which needs to be diagnosed and diagnosed in time. In the process, it is necessary to pay attention to postoperative care and prevention** to avoid aggravation of the condition and life-threatening.