Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report

<p>Abstract</p> <p>Introduction</p> <p>Heterotopic gastric mucosa is described almost everywhere in the gastrointestinal tract, from the oral cavity to the rectum. The occurrence of heterotopic gastric tissue in the gallbladder is rare. A choristoma can be defined as a...

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Main Authors: Popkharitov Angel I, Gulubova Maya V, Dandov Angel D, Sivrev Dimitar P
Format: Article
Language:English
Published: BMC 2008-05-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/2/1/173
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spelling doaj-e56b83aa925a424a9efeb627d3f29c852020-11-24T21:56:32ZengBMCJournal of Medical Case Reports1752-19472008-05-012117310.1186/1752-1947-2-173Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case reportPopkharitov Angel IGulubova Maya VDandov Angel DSivrev Dimitar P<p>Abstract</p> <p>Introduction</p> <p>Heterotopic gastric mucosa is described almost everywhere in the gastrointestinal tract, from the oral cavity to the rectum. The occurrence of heterotopic gastric tissue in the gallbladder is rare. A choristoma can be defined as a new growth developing from a displaced anlage not normally present in the anatomical site where it developed. We present an extremely uncommon case of a cyst (choristoma) attached to the gallbladder, which contained gastric and intestinal mucosa.</p> <p>Case presentation</p> <p>A 33-year-old woman was hospitalized with clinical symptoms of chronic cholecystitis. The laboratory findings were within the normal range. Abdominal ultrasonography revealed a thickened gallbladder wall and a stone in the cystic duct was suspected. In the course of laparoscopic cholecystectomy, a cyst was visualized in the vicinity of the duct and the gallbladder neck. Microscopic examination of the removed cyst revealed evidence of gastric, duodenal and small-intestinal mucosa. The immunohistochemical study revealed many endocrine cells, which were positive for several endocrine cell markers such as chromogranin, serotonin, gastrin and so on. It can be inferred that the observed cyst had arisen from the foregut early in the development of the gastrointestinal tract.</p> <p>Conclusion</p> <p>The presence of endocrine cells together with epithelial cells supports the hypothesis that these had developed simultaneously, and that the endocrine cells had probably supported the development of the epithelial cells by the release of hormones and growth factors. To the best of the authors' knowledge, this report is the first to report a gastrointestinal cyst choristoma with endocrine cells in the region of the cystic duct and gallbladder.</p> http://www.jmedicalcasereports.com/content/2/1/173
collection DOAJ
language English
format Article
sources DOAJ
author Popkharitov Angel I
Gulubova Maya V
Dandov Angel D
Sivrev Dimitar P
spellingShingle Popkharitov Angel I
Gulubova Maya V
Dandov Angel D
Sivrev Dimitar P
Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
Journal of Medical Case Reports
author_facet Popkharitov Angel I
Gulubova Maya V
Dandov Angel D
Sivrev Dimitar P
author_sort Popkharitov Angel I
title Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
title_short Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
title_full Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
title_fullStr Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
title_full_unstemmed Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
title_sort heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2008-05-01
description <p>Abstract</p> <p>Introduction</p> <p>Heterotopic gastric mucosa is described almost everywhere in the gastrointestinal tract, from the oral cavity to the rectum. The occurrence of heterotopic gastric tissue in the gallbladder is rare. A choristoma can be defined as a new growth developing from a displaced anlage not normally present in the anatomical site where it developed. We present an extremely uncommon case of a cyst (choristoma) attached to the gallbladder, which contained gastric and intestinal mucosa.</p> <p>Case presentation</p> <p>A 33-year-old woman was hospitalized with clinical symptoms of chronic cholecystitis. The laboratory findings were within the normal range. Abdominal ultrasonography revealed a thickened gallbladder wall and a stone in the cystic duct was suspected. In the course of laparoscopic cholecystectomy, a cyst was visualized in the vicinity of the duct and the gallbladder neck. Microscopic examination of the removed cyst revealed evidence of gastric, duodenal and small-intestinal mucosa. The immunohistochemical study revealed many endocrine cells, which were positive for several endocrine cell markers such as chromogranin, serotonin, gastrin and so on. It can be inferred that the observed cyst had arisen from the foregut early in the development of the gastrointestinal tract.</p> <p>Conclusion</p> <p>The presence of endocrine cells together with epithelial cells supports the hypothesis that these had developed simultaneously, and that the endocrine cells had probably supported the development of the epithelial cells by the release of hormones and growth factors. To the best of the authors' knowledge, this report is the first to report a gastrointestinal cyst choristoma with endocrine cells in the region of the cystic duct and gallbladder.</p>
url http://www.jmedicalcasereports.com/content/2/1/173
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