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A rare case of a congenital pancreatic duplication cyst in an infant complicated by an upper GI bleed, pancreatitis, cyst infection and gastric outlet obstruction.
Cadili, Lina; Cullen, Krystal L; Finn, Nicola J; Singh, Andrew; Webber, Eric; Hayashi, Allen H.
Afiliação
  • Cadili L; Division of General Surgery, Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Cullen KL; Department of Pediatrics, Faculty of Medicine, University of British Columbia, Victoria, British Columbia, Canada.
  • Finn NJ; Department of Radiology, Faculty of Medicine, University of British Columbia, Victoria, British Columbia, Canada.
  • Singh A; Division of Gastroenterology, Department of Medicine, Faculty of Medicine, University of British Columbia, Victoria, British Columbia, Canada.
  • Webber E; Division of General Surgery, Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Hayashi AH; Division of General Surgery, Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
J Surg Case Rep ; 2022(7): rjac326, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35813453
ABSTRACT
Enteric duplication cysts are rare congenital entities most commonly found in the esophagus, ileum or colon but can be in remote locations such as the biliary tree, liver or pancreas. Pancreatic duplication cysts are very uncommon and usually present in adulthood with pancreatitis or abdominal pain. Here, we present a unique and complex case of an infant with a pancreatic duplication cyst initially presenting with an upper gastrointestinal bleed followed by pancreatitis, cyst infection and gastric outlet obstruction.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article