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A rare gallbladder ciliated foregut cyst in chronic cholecystitis
INTRODUCTION: Ciliated foregut cysts (CFC) are rare anomalies due to aberrant embryological development. It is thought to arise from a remnant of the embryologic foregut. The solitary cysts are characterised by ciliated pseudostratified columnar epithelium. They are usually located above the diaphra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818304/ https://www.ncbi.nlm.nih.gov/pubmed/26890682 http://dx.doi.org/10.1016/j.ijscr.2016.01.023 |
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author | Lee, Mee-Jin Salinas, James Varikatthas, Winny Alsnih, Ghiyath |
author_facet | Lee, Mee-Jin Salinas, James Varikatthas, Winny Alsnih, Ghiyath |
author_sort | Lee, Mee-Jin |
collection | PubMed |
description | INTRODUCTION: Ciliated foregut cysts (CFC) are rare anomalies due to aberrant embryological development. It is thought to arise from a remnant of the embryologic foregut. The solitary cysts are characterised by ciliated pseudostratified columnar epithelium. They are usually located above the diaphragm but they can also arise in relation to the liver, gallbladder and pancreas. PRESENTATION OF CASE: We present the first ciliated foregut cyst of the gallbladder case reported in Australia, and the ninth known case to be reported worldwide. A 61-year-old male with chronic cholecystitis and cholelithiasis underwent an elective laparoscopic cholecystectomy and intraoperative cholangiogram. Intraoperatively, ‘out-pouching’ was noted on the lateral border of the gallbladder. Microscopically the histopathology showed that the cyst was lined by ciliated columnar epithelium the characteristic feature of a ciliated foregut cyst. DISCUSSION: To date only 8 cases of these ciliated foregut cysts in the gallbladder have been reported in literature. Our case is the first reported in Australia. It is unique in that the patient was an older male as opposed to most other previous cases, which were younger females. These cysts can be difficult to distinguish from neoplasms clinically and radiographically. Reports have shown that these cysts may become dysplastic and is best excised when discovered. CONCLUSION: Despite the rarity of CFCs and their potential to mimic malignancy, we propose awareness and understanding of the management for them—being excision and hopefully not cause any confusion or devastatingly allow it to become malignant. |
format | Online Article Text |
id | pubmed-4818304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48183042016-04-14 A rare gallbladder ciliated foregut cyst in chronic cholecystitis Lee, Mee-Jin Salinas, James Varikatthas, Winny Alsnih, Ghiyath Int J Surg Case Rep Case Report INTRODUCTION: Ciliated foregut cysts (CFC) are rare anomalies due to aberrant embryological development. It is thought to arise from a remnant of the embryologic foregut. The solitary cysts are characterised by ciliated pseudostratified columnar epithelium. They are usually located above the diaphragm but they can also arise in relation to the liver, gallbladder and pancreas. PRESENTATION OF CASE: We present the first ciliated foregut cyst of the gallbladder case reported in Australia, and the ninth known case to be reported worldwide. A 61-year-old male with chronic cholecystitis and cholelithiasis underwent an elective laparoscopic cholecystectomy and intraoperative cholangiogram. Intraoperatively, ‘out-pouching’ was noted on the lateral border of the gallbladder. Microscopically the histopathology showed that the cyst was lined by ciliated columnar epithelium the characteristic feature of a ciliated foregut cyst. DISCUSSION: To date only 8 cases of these ciliated foregut cysts in the gallbladder have been reported in literature. Our case is the first reported in Australia. It is unique in that the patient was an older male as opposed to most other previous cases, which were younger females. These cysts can be difficult to distinguish from neoplasms clinically and radiographically. Reports have shown that these cysts may become dysplastic and is best excised when discovered. CONCLUSION: Despite the rarity of CFCs and their potential to mimic malignancy, we propose awareness and understanding of the management for them—being excision and hopefully not cause any confusion or devastatingly allow it to become malignant. Elsevier 2016-01-22 /pmc/articles/PMC4818304/ /pubmed/26890682 http://dx.doi.org/10.1016/j.ijscr.2016.01.023 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Lee, Mee-Jin Salinas, James Varikatthas, Winny Alsnih, Ghiyath A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title | A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title_full | A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title_fullStr | A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title_full_unstemmed | A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title_short | A rare gallbladder ciliated foregut cyst in chronic cholecystitis |
title_sort | rare gallbladder ciliated foregut cyst in chronic cholecystitis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818304/ https://www.ncbi.nlm.nih.gov/pubmed/26890682 http://dx.doi.org/10.1016/j.ijscr.2016.01.023 |
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