S3472 Santorinicele: A Rare Cause of Pancreatic Duct Dilation

Introduction: A diffuse dilated pancreatic duct can be caused by different conditions, including pancreatic cancer, chronic pancreatitis and main duct intraductal papillary mucinous neoplasm (IPMN). Herein, we describe a case of a rare cause of dilation of the pancreatic duct. Case Description/Methods: A 69-year-old woman with type 2 diabetes mellitus presented with persistent diarrhea. After exhaustive work-up, this was determined to be secondary to metformin. Her workup included a computed tomography of the abdomen that showed pancreatic atrophy and ductal dilation. A subsequent magnetic resonance cholangiopancreatography (MRCP) showed pancreas divisum, diffuse main duct dilation, and a 7 × 10 × 11 mm cystic lesion in the minor papilla suspicious for a santorinicele. An endoscopic ultrasound was done that showed no pancreatic malignancy, and no sampling was performed of the cystic lesion. The patient was followed with cross-sectional images, and eventually a MRCP done 2 years later showed enlargement of the santorinicele up to 25 mm and main duct dilation of 9 mm. Given the suspicion for an IPMN, a repeated endoscopic ultrasound (EUS) was performed, showing a cyst measuring 19 × 18 mm in the minor papilla with ductal dilation up to 7.1 mm in the head. Fine needle aspiration of the cystic lesion showed a low CEA (3.4 ng/mL) and cytology negative for malignancy. ERCP was later performed that confirmed the cystic lesion in the minor papilla communicating with the main pancreatic duct and consistent with a santorinicele. This was treated with a minor papilla sphincterotomy. In addition, a pancreatoscopy was performed that demonstrated a normal pancreatic duct epithelium. On follow-up MRCP a year later, the cystic lesion was no longer visible. Discussion: A santorinicele is a focal cystic dilatation of the terminal dorsal pancreatic duct and is often associated with ductal anomalies (e.g., pancreas divisum). It is thought to result from increased intraductal pressure due to relative stenosis at the minor papilla. Endoscopic interventions such as sphincterotomy can relieve ductal obstruction and symptoms. Given the cystic appearance, IPMN must be ruled out due to its malignant potential. In this case, the EUS findings and negative cytology excluded malignancies and guided therapeutic intervention.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001141348.62744.70
Primary Topic
Pediatric Hepatobiliary Diseases and Treatments
Type
article
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article

S3472 Santorinicele: A Rare Cause of Pancreatic Duct Dilation

David Guevara-Lazo, Jorge D. Machicado
The American Journal of Gastroenterology
Pediatric Hepatobiliary Diseases and Treatments
article

S3472 Santorinicele: A Rare Cause of Pancreatic Duct Dilation

David Guevara-Lazo, Jorge D. Machicado
article en

Abstract

Introduction: A diffuse dilated pancreatic duct can be caused by different conditions, including pancreatic cancer, chronic pancreatitis and main duct intraductal papillary mucinous neoplasm (IPMN). Herein, we describe a case of a rare cause of dilation of the pancreatic duct. Case Description/Methods: A 69-year-old woman with type 2 diabetes mellitus presented with persistent diarrhea. After exhaustive work-up, this was determined to be secondary to metformin. Her workup included a computed tomography of the abdomen that showed pancreatic atrophy and ductal dilation. A subsequent magnetic resonance cholangiopancreatography (MRCP) showed pancreas divisum, diffuse main duct dilation, and a 7 × 10 × 11 mm cystic lesion in the minor papilla suspicious for a santorinicele. An endoscopic ultrasound was done that showed no pancreatic malignancy, and no sampling was performed of the cystic lesion. The patient was followed with cross-sectional images, and eventually a MRCP done 2 years later showed enlargement of the santorinicele up to 25 mm and main duct dilation of 9 mm. Given the suspicion for an IPMN, a repeated endoscopic ultrasound (EUS) was performed, showing a cyst measuring 19 × 18 mm in the minor papilla with ductal dilation up to 7.1 mm in the head. Fine needle aspiration of the cystic lesion showed a low CEA (3.4 ng/mL) and cytology negative for malignancy. ERCP was later performed that confirmed the cystic lesion in the minor papilla communicating with the main pancreatic duct and consistent with a santorinicele. This was treated with a minor papilla sphincterotomy. In addition, a pancreatoscopy was performed that demonstrated a normal pancreatic duct epithelium. On follow-up MRCP a year later, the cystic lesion was no longer visible. Discussion: A santorinicele is a focal cystic dilatation of the terminal dorsal pancreatic duct and is often associated with ductal anomalies (e.g., pancreas divisum). It is thought to result from increased intraductal pressure due to relative stenosis at the minor papilla. Endoscopic interventions such as sphincterotomy can relieve ductal obstruction and symptoms. Given the cystic appearance, IPMN must be ruled out due to its malignant potential. In this case, the EUS findings and negative cytology excluded malignancies and guided therapeutic intervention.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 52%
Pediatric Hepatobiliary Diseases and Treatments
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