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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...

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Autores principales: Lee, Mee-Jin, Salinas, James, Varikatthas, Winny, Alsnih, Ghiyath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
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.
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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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