ArticleAnnals of the Royal College of Surgeons of England2012
Intraductal papillary mucinous neoplasm of the oesophagus: an unusual case of dysphagia.
Article in Annals of the Royal College of Surgeons of England, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 9 citations in OpenAlex.
- Multidisciplinary Treatment for Advanced Pancreatic Adenocarcinoma Arising from Esophageal Heterotopic Pancreas in a Young Adult: A Case Report.Surgical case reports · 2026Article
- Esophageal Heterotopic Pancreas in an Asymptomatic 2-Year-Old With VACTERL Association.JPGN reports · 2023Article
- Heterotopic Pancreas in the Esophagus: What Do We Know?-A Review of the Literature.Gastro hep advances · 2023Article
- Esophageal Pancreatic Acinar Heterotopia: Premalignant or Benign.Journal of medical cases · 2022Article
- Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma-A rare case report and comprehensive literature review.Thoracic cancer · 2022Review
- Heterotopic Pancreas Located at the Gastroesophageal Junction in a Hiatal Hernia: A Case Report.Cureus · 2021Article
- A Case of Heterotopic Pancreatic Tissue Discovered in the Distal Esophagus.Case reports in gastrointestinal medicine · 2020Article
- Intraductal papillary mucinous neoplasm of the ileal heterotopic pancreas in a patient with hereditary non-polyposis colorectal cancer: A case report.World journal of gastroenterology · 2015Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
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