Intestinal duplication cysts are rare congenital lesions of the digestive tract in infants and young children. This abnormality can occur at any segment, from the mouth to the anus, with very different clinical manifestations. Depending on the age, physical condition and location of the lesion of the child, the final treatment is always surgical removal of the entire segment of the duplication. In which, laparoscopic surgery is always the preferred method.

Double intestinal disease is a rare congenital gastrointestinal malformation in children, when double intestine can cause some dangerous complications. Double intestinal disease can be found anywhere in the digestive tract, in which the most common is double intestine, accounting for over 70% of cases.

Intestinal duplication cyst is a congenital anomaly in which a normal segment of the intestine appears with another segment of the intestine of a similar nature. However, when this double intestinal segment causes pathology, surgical intervention will always be indicated. Compared with endoscopic surgery, open surgery to treat intestinal duplication creates some favorable conditions and will be considered as the first indication in lesions showing that the advantages will be superior.