Annular pancreas overview

Annular pancreas is a rare condition in which the second part of the duodenum is surrounded by a ring of pancreatic tissue continuous with the head of the pancreas. This portion of the pancreas can constrict the duodenum and block or impair the flow of food to the rest of the intestines. It occurs in 1 out of 12,000 to 15,000 newborns.^{[1] [2]}

Annular pancreas is typically associated with abnormal embryological development, however adult cases can develop. It can result from growth of a bifid ventral pancreatic bud around the duodenum, where the parts of the bifid ventral bud fuse with the dorsal bud, forming a pancreatic ring. It can also result if the ventral pancreatic bud fails to fully rotate, so it remains on the right or if the dorsal bud rotates in the wrong direction, such that the duodenum is surrounded by pancreatic tissue. Blockage of the duodenum develops if inflammation (pancreatitis) develops in the annular pancreas.

Postnatal diagnostic procedures include abdominal x-ray and ultrasound, CT scan, and upper GI and small bowel series

CT or MRI studies may show normal pancreatic tissue, with or without a small pancreatic duct, encircling the duodenum.

Surgical resection is recommended for symptomatic cases. Treatment usually is bypassing the obstructed segment of duodenum by duodeno-doudenostomy. Another approach is laparoscopicgastrojejunostomy.^[3]

Template:Congenital malformations and deformations of digestive system

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