Korean J Intern Med.  2006 Dec;21(4):236-239. 10.3904/kjim.2006.21.4.236.

Agenesis of the Dorsal Pancreas: A Case Report and Review of the Literature

• Joo YE
• Kang HC
• Kim HS
• Choi SK
• Rew JS
• Chung MY
• Kim SJ

• KMID: 759857
• DOI: http://doi.org/10.3904/kjim.2006.21.4.236

Abstract

Partial or complete agenesis of the dorsal pancreas is a rare congenital anomaly that results from the embryological failure of the dorsal pancreatic bud to form the body and tail of the pancreas. To date, four cases have been reported in Korea. We report an additional case; a 25-year-old woman presented with diabetes mellitus and abdominal pain. Abdominal computed tomography (CT) revealed a normal-appearing pancreatic head, but the body and tail were not visualized. Endoscopic cholangiopancreatogram (ERCP) revealed a short pancreatic duct in the uncinate process and the head and the duct of Santorini draining into the minor papilla. Abdominal magnetic resonance imaging (MRI) findings were similar to the CT and ERCP results. The patient was diagnosed with partial agenesis of the dorsal pancreas by CT, ERCP and MRI.

Keyword

Anomaly; Agenesis; Dorsal pancreas

MeSH Terms

Tomography, X-Ray Computed
Pancreatic Diseases/*congenital/diagnosis
Pancreas/*abnormalities
Magnetic Resonance Imaging
Humans
Female
Diagnosis, Differential
Cholangiopancreatography, Endoscopic Retrograde
Adult