{"title":"Spontaneous fistulization of a giant pancreatic pseudocyst into the duodenum following acute pancreatitis: a case report.","authors":"Bikash Kumar Shah, Adesh Kantha, Abhisekh Bhattarai","doi":"10.1097/MS9.0000000000005650","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Pancreatic pseudocysts are well-recognized sequelae of pancreatitis, but giant pseudocysts (>10 cm) are uncommon and rarely resolve through spontaneous fistulization. Spontaneous internal rupture into the gastrointestinal tract happens in less than 3% of cases and typically requires surgical or endoscopic intervention.</p><p><strong>Case presentation: </strong>We report the case of a 40-year-old male with a history of alcohol use who developed a giant pancreatic pseudocyst (22 × 12 cm) following acute pancreatitis. He presented with abdominal discomfort, early satiety, and vomiting. Imaging revealed a massive cyst compressing the stomach and duodenum. Although initially managed conservatively, the patient later experienced episodes of severe abdominal pain and coffee-ground vomiting.</p><p><strong>Clinical discussion: </strong>Spontaneous internal drainage of a giant pancreatic pseudocyst into the duodenum is very rare. This case highlights the potential for non-operative management in carefully selected, clinically stable patients, despite the size of the lesion and the risk of complications.</p><p><strong>Conclusion: </strong>We describe an unusual case of a giant pancreatic pseudocyst that resolved spontaneously through cystoduodenal fistulization. Conservative management led to full recovery, underscoring the importance of individualized treatment strategies in pancreatic pseudocyst management.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"88 10","pages":"6846-6850"},"PeriodicalIF":1.6000,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13657579/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Medicine and Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/MS9.0000000000005650","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Pancreatic pseudocysts are well-recognized sequelae of pancreatitis, but giant pseudocysts (>10 cm) are uncommon and rarely resolve through spontaneous fistulization. Spontaneous internal rupture into the gastrointestinal tract happens in less than 3% of cases and typically requires surgical or endoscopic intervention.
Case presentation: We report the case of a 40-year-old male with a history of alcohol use who developed a giant pancreatic pseudocyst (22 × 12 cm) following acute pancreatitis. He presented with abdominal discomfort, early satiety, and vomiting. Imaging revealed a massive cyst compressing the stomach and duodenum. Although initially managed conservatively, the patient later experienced episodes of severe abdominal pain and coffee-ground vomiting.
Clinical discussion: Spontaneous internal drainage of a giant pancreatic pseudocyst into the duodenum is very rare. This case highlights the potential for non-operative management in carefully selected, clinically stable patients, despite the size of the lesion and the risk of complications.
Conclusion: We describe an unusual case of a giant pancreatic pseudocyst that resolved spontaneously through cystoduodenal fistulization. Conservative management led to full recovery, underscoring the importance of individualized treatment strategies in pancreatic pseudocyst management.