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Complex Pancreaticobiliary Maljunction with Pancreas Divisum and Obstructive Pseudocyst
Jaren T Meldrum1, Benjamin D Tabak2, Christopher A Roberts3
1Departments of Radiology, Tripler Army Medical Center, 1 Jarrett White Rd., Honolulu, Hawaii, United States.
Journal of Clinical Imaging Science
|June 18, 2020
Summary
Complex pancreaticobiliary maljunction (PBM), a rare congenital anomaly, can present with acute pancreatitis and pseudocysts. Surgical management is crucial due to high post-operative complication risks in Type D PBM.
Area of Science:
- Gastroenterology and Hepatobiliary Surgery
- Congenital Anomalies
- Pancreaticobiliary Disorders
Background:
- Pancreaticobiliary maljunction (PBM) is a congenital condition where bile and pancreatic ducts join outside the duodenum.
- Complex Type D PBM, often associated with other anomalies, is rare and carries significant clinical implications.
Observation:
- A rare case of complex Type D PBM with pancreas divisum is presented.
- The patient exhibited acute pancreatitis and obstructive symptoms due to a pancreatic pseudocyst.
Findings:
- This case highlights the diagnostic and management challenges of complex PBM.
- The association with pancreas divisum and pseudocyst formation is noted.
Implications:
- Complex PBM requires careful surgical consideration due to a high risk of post-operative complications.
- Understanding these rare anomalies is vital for effective patient management and surgical planning.
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