Gastroesophageal junction pancreatic heterotopia/metaplasia: a case series.

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-06-09 eCollection Date: 2025-06-01 DOI:10.1093/jscr/rjaf390
Moaaz Amir, Salwa Sheikh
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引用次数: 0

Abstract

Gastroesophageal junction pancreatic heterotopia is an uncommon congenital condition where pancreatic tissue is present outside its normal anatomical location. We present a case series of four patients who have presented with nonspecific, vague gastrointestinal symptoms that included abdominal pain, dyspepsia, and heartburn. Endoscopy was performed and revealed irregular Z-lines in three out of the four patients, with high suspicion of Barrett's esophagus. Further histopathologic evaluation confirmed ectopic pancreatic tissue in all four patients, two of whom had mild chronic inflammation, another presented with chronic gastritis as well as reflux esophagitis, and the last patient exhibited intestinal metaplasia. Also, three patients were treated with proton pump inhibitors and were kept under constant surveillance, while one patient was lost to follow-up. Pancreatic heterotopia involving the gastroesophageal junction is a rare presentation that usually goes unnoticed due to its asymptomatic nature. It is important that clinicians recognize such presentations to provide optimal treatment.

胃食管交界处胰腺异位/化生:一个病例系列。
胃食管交界处胰腺异位是一种罕见的先天性疾病,胰腺组织存在于其正常解剖位置之外。我们提出了一个病例系列,其中4例患者表现为非特异性、模糊的胃肠道症状,包括腹痛、消化不良和胃灼热。内镜检查发现4例患者中有3例出现不规则z线,高度怀疑为Barrett食管。进一步的组织病理学检查证实所有4例患者胰腺组织异位,其中2例有轻度慢性炎症,1例表现为慢性胃炎和反流性食管炎,最后1例表现为肠化生。此外,三名患者接受质子泵抑制剂治疗并持续监测,而一名患者没有随访。胰腺异位累及胃食管交界处是一种罕见的表现,通常由于其无症状的性质而被忽视。重要的是,临床医生认识到这种表现,以提供最佳的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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