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Heterotopic pancreas - An expert in hide and seek
Ko-Ping Tiang1, Kamarajan Ramayah1, Hang Wai Yu1
1Department of Surgery, HPB Unit, University of Malaya Medical Centre, Kuala Lumpur, Malaysia.
International Journal of Surgery Case Reports
|October 8, 2024
Summary
Heterotopic pancreas, a rare condition, is often asymptomatic and difficult to diagnose pre-operatively. Surgical resection remains the definitive treatment for symptomatic cases.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Diagnostic Imaging
Background:
- Heterotopic pancreas is a rare congenital anomaly where pancreatic tissue is found outside its normal location.
- Common sites include the upper gastrointestinal tract, but thoracic, splenic, and renal locations are exceptionally rare.
- Most patients with heterotopic pancreas are asymptomatic, complicating early diagnosis.
Observation:
- A patient presented with postprandial abdominal pain and weight loss, with imaging revealing a duodenal growth.
- Standard imaging and PET scans did not show metabolic activity, posing diagnostic challenges.
- Surgical intervention (laparotomy, small bowel resection) was performed due to symptomatic presentation.
Findings:
- Histopathological examination (HPE) confirmed the presence of heterotopic pancreas.
- Heterotopic pancreas can mimic other gastrointestinal pathologies and may lead to complications like pancreatitis or malignancy.
- Diagnostic tools like endoscopy and CT imaging have limitations in detecting these anomalies.
Implications:
- This case highlights the diagnostic challenges associated with heterotopic pancreas, especially in symptomatic individuals.
- Early recognition of common locations and imaging characteristics is crucial for diagnosis.
- Surgical resection is the definitive management for symptomatic heterotopic pancreas.
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