scholarly journals Intraductal papillary mucinous neoplasm of the oesophagus: an unusual case of dysphagia

2012 ◽  
Vol 94 (2) ◽  
pp. e92-e94 ◽  
Author(s):  
E Crighton ◽  
A Botha

We report the case of a 58-year-old woman presenting with dysphagia secondary to an intraductal papillary mucinous neoplasm arising from a heterotopic pancreas in the oesophageal wall. This was successfully treated with a laparoscopic/thoracoscopic ivor Lewis oesophagectomy. Dysphagia is the most common symptom of oesophageal tumours regardless of aetiology of the tumour and can be treated successfully with surgical resection. Through an extensive search of the literature, we found that a heterotopic pancreas in the oesophagus is extremely rare with only ten cases being reported. We describe what we believe to be the first case of a heterotopic pancreas in the oesophagus transforming into an intraductal papillary mucinous neoplasm.

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Alistair J. Lawrence ◽  
Aducio Thiessen ◽  
Amy Morse ◽  
A. M. James Shapiro

We report a unique first case of benign heterotopic pancreas arising within the proximal hepatic bile duct, containing a focus of intraductal papillary mucinous neoplasm (IPMN). The condition was diagnosed on pathological explant after left hepatic lobectomy with total extrahepatic bile duct excision.


2012 ◽  
Vol 46 (1) ◽  
pp. 96 ◽  
Author(s):  
Ju Young Song ◽  
Jee Young Han ◽  
Sun Keun Choi ◽  
Lucia Kim ◽  
Suk Jin Choi ◽  
...  

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Haruna Komatsubara ◽  
Hiroyuki Kato ◽  
Daisuke Noguchi ◽  
Kazuyuki Gyoten ◽  
Aoi Hayasaki ◽  
...  

Abstract Background 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. 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. Conclusions To 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.


Pancreas ◽  
2012 ◽  
Vol 41 (1) ◽  
pp. 137-141 ◽  
Author(s):  
Guillaume Passot ◽  
Roger Lebeau ◽  
Valérie Hervieu ◽  
Thierry Ponchon ◽  
Franck Pilleul ◽  
...  

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