Abstract

BackgroundWe experienced a rare case of intraductal papillary mucinous neoplasm arising from Santorini’s duct (SD) forming a tumor protruding into the duodenum .Case presentationA 71-year-old woman was incidentally diagnosed with a 3 cm type Isp polypoid tumor in the second portion of the duodenum at another hospital. Enhanced CT and endoscopic ultrasound revealed that the origin of this protruding tumor was arising from SD and that the tumor mimicked a pedunculated duodenal tumor. Our preoperative diagnosis was a malignant pancreatic tumor arising from SD with invasion into the duodenum. She underwent a subtotal stomach-preserving pancreaticoduodenectomy, and the resected specimen showed a 25 mm tumor protruding into the duodenum with a villous surface. The pathological findings revealed that the tumor was intraductal papillary mucinous adenoma (IPMA) arising from SD.ConclusionsTo the best of our knowledge, this is the first case of IPMA protruding into the duodenal lumen from SD, although most of the tumors arising from SD have been reported to be malignant.

Highlights

  • We experienced a rare case of intraductal papillary mucinous neoplasm arising from Santorini’s duct (SD) forming a tumor protruding into the duodenum .Case presentation: A 71-year-old woman was incidentally diagnosed with a 3 cm type Isp polypoid tumor in the second portion of the duodenum at another hospital

  • To the best of our knowledge, this is the first case of intraductal papillary mucinous adenoma (IPMA) protruding into the duodenal lumen from SD, most of the tumors arising from SD have been reported to be malignant

  • Intraductal papillary mucinous neoplasm (IPMN) are usually classified into three types based on imaging studies and/or histology based on the origin of the tumor whether it arises from the main pancreatic duct (MPD), branches of the main ductal system, or both of them

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Summary

Conclusions

To the best of our knowledge, this is the first case of IPMA protruding into the duodenal lumen from SD, most of the tumors arising from SD have been reported to be malignant.

Background
Findings
Discussion and conclusions

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