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A Case of Heterotopic Pancreatic Tissue Discovered in the Distal Esophagus.
Shamoon, Dema; Sostre, Vanessa; Patel, Varun; Volfson, Ariy.
Affiliation
  • Shamoon D; Department of Medicine, St. Joseph's University Medical Center, Paterson, NJ, USA.
  • Sostre V; Department of Medicine, St. Joseph's University Medical Center, Paterson, NJ, USA.
  • Patel V; Division of Gastroenterology and Hepatology, St. Joseph's University Medical Center, Paterson, NJ, USA.
  • Volfson A; Division of Gastroenterology and Hepatology, St. Joseph's University Medical Center, Paterson, NJ, USA.
Case Rep Gastrointest Med ; 2020: 4695184, 2020.
Article in En | MEDLINE | ID: mdl-32328316
Heterotopic pancreas (HP) is a congenital abnormality that represents ectopic pancreatic tissue that does not have anatomic, vascular, or ductal continuity. The prevalence of HP is 0.55% to 13.7% on autopsy, 0.2% to 0.5% of abdominal operations, and 0.9% of gastrectomies. It is commonly found in the stomach, duodenum, and proximal jejunum. Only 15 cases have been reported in the medical literature regarding involvement of the esophagus. Treatment depends on symptoms and location. In asymptomatic patients, simple observation may be sufficient; however, in those who are symptomatic, surgery may be warranted. We present a case of a 70-year-old male with heartburn, nausea, and abdominal bloating who underwent a diagnostic esophagogastroduodenoscopy (EGD) and was found to have HP on histology in the distal esophagus. In our case, symptoms were treated conservatively and successfully with a proton pump inhibitor (PPI).

Full text: 1 Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Case Rep Gastrointest Med Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Case Rep Gastrointest Med Year: 2020 Type: Article Affiliation country: United States