Literature DB >> 8944044

Prevalence and significance of pancreatic acinar metaplasia at the gastroesophageal junction.

H H Wang1, J M Zeroogian, S J Spechler, R K Goyal, D A Antonioli.   

Abstract

Pancreatic acinar metaplasia (PAM), defined as nodules of glandular tissue forming acini composed of cells with coarse apical eosinophilic granules, with or without mucous cells, was recently recognized in gastric mucosa, but its significance is not known. As part of a study on intestinal metaplasia at the gastroesophageal junction (GEJ), we evaluated the prevalence and clinical and histologic correlates of PAM in biopsy specimens from the gastroesophageal squamocolumnar junction. All adult patients having elective upper gastrointestinal endoscopy over a 6-month period were invited to participate. Clinical data and endoscopic findings were recorded. Biopsy specimens, obtained from both sides of the apparent squamocolumnar junction, were processed routinely and reviewed (without knowledge of the clinical data) to evaluate types of epithelium, types and degree of inflammation, and the presence of PAM. The presence or absence of PAM was then correlated with the other histologic findings and with the clinical and endoscopic data. The study comprised 155 patients (79 women, 76 men; 139 white patients, nine black patients, and seven patients of other ethnic groups). Their mean age was 52 years (range: 18-89 years). PAM was present in 37 patients (24%). PAM was not associated with any of the reported symptoms, endoscopic evidence of esophagitis or columnar epithelium in the distal esophagus, or any of the histologic features evaluated, including active esophagitis, intestinal metaplasia at the GEJ, active and chronic gastritis, intestinal metaplasia in the stomach, and Helicobacter infection. Although PAM is present in a considerable proportion (24%) of patients with mucosal biopsy specimens from the squamocolumnar junction, it appears to be an incidental finding unrelated to clinical or histologic abnormalities. We therefore suggest a congenital, rather than an acquired, origin for this entity.

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Year:  1996        PMID: 8944044     DOI: 10.1097/00000478-199612000-00010

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  9 in total

1.  Cardiac mucosa at the gastroesophageal junction: An Eastern perspective.

Authors:  Ahrong Kim; Won-Young Park; Nari Shin; Hyun Jung Lee; Young Keum Kim; So Jeong Lee; Cheong-Soo Hwang; Do Youn Park; Gwang Ha Kim; Bong Eun Lee; Hong-Jae Jo
Journal:  World J Gastroenterol       Date:  2015-08-14       Impact factor: 5.742

2.  The gastric cardia in gastro-oesophageal disease.

Authors:  H M el-Zimaity; V J Verghese; J Ramchatesingh; D Y Graham
Journal:  J Clin Pathol       Date:  2000-08       Impact factor: 3.411

Review 3.  Immunological and morphogenic basis of gastric mucosa atrophy and metaplasia.

Authors:  Gerhard Faller; Thomas Kirchner
Journal:  Virchows Arch       Date:  2004-12-04       Impact factor: 4.064

4.  Barrett's Esophagus without dysplasia: wait or ablate?

Authors:  Stuart Jon Spechler
Journal:  Dig Dis Sci       Date:  2011-07       Impact factor: 3.199

5.  Pancreatic acinar metaplasia in the distal oesophagus and the gastric cardia: prevalence, predictors and relation to GORD.

Authors:  Johan Johansson; Hans-Olof Håkansson; Lennart Mellblom; Antti Kempas; Gerhard Kjellén; Lars Brudin; Fredrik Granath; Karl-Erik Johansson; Olof Nyrén
Journal:  J Gastroenterol       Date:  2009-12-15       Impact factor: 7.527

6.  Pancreatic-type mixed acinar-endocrine carcinoma with alpha-fetoprotein production arising from the stomach: a report of an extremely rare case.

Authors:  Kimihide Kusafuka; Etsuro Bando; Koji Muramatsu; Hiroaki Ito; Yutaka Tanizawa; Taiichi Kawamura; Toru Mochizuki; Masanori Terashima; Takashi Nakajima
Journal:  Med Mol Morphol       Date:  2009-09-26       Impact factor: 2.309

7.  Pancreatic acinar cells--a normal finding at the gastroesophageal junction? Data from a prospective Central European multicenter study.

Authors:  Nora I Schneider; Wolfgang Plieschnegger; Michael Geppert; Bernd Wigginghaus; Gabriele M Höss; Andreas Eherer; Eva-Maria Wolf; Peter Rehak; Michael Vieth; Cord Langner
Journal:  Virchows Arch       Date:  2013-08-29       Impact factor: 4.064

8.  Development of Pancreatic Acinar Cell Metaplasia During Gastric Repair in a Rat Duodenal Contents Reflux Model.

Authors:  Yasuhiro Wada; Ken-Ichi Mukaisho; Shunpei Kanai; Takahisa Nakayama; Masahide Fukuda; Kazuhiro Mizukami; Tadayoshi Okimoto; Masaaki Kodama; Hiroyuki Sugihara; Kazunari Murakami; Ryoji Kushima
Journal:  Dig Dis Sci       Date:  2020-05-21       Impact factor: 3.199

9.  Esophageal Pancreatic Acinar Heterotopia: Premalignant or Benign.

Authors:  Krystal Mills; Temitayo Gboluaje; Timothy Sobukonla; Melvin Simien
Journal:  J Med Cases       Date:  2022-06-11
  9 in total

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