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Mesothelial inclusion cyst: a rare occurrence

Mesothelial inclusion cyst is a rare benign tumour that has only 130 cases reported in the literature. Accurate diagnosis and optimal management of this condition remains uncertain. We report a 51-year-old African gentleman, whom presents with abdominal pain and constipation. A computed tomography s...

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Detalles Bibliográficos
Autores principales: Soon, David SC, Shilton, Hamish, Andrabi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5165051/
https://www.ncbi.nlm.nih.gov/pubmed/27994008
http://dx.doi.org/10.1093/jscr/rjw213
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author Soon, David SC
Shilton, Hamish
Andrabi, Ali
author_facet Soon, David SC
Shilton, Hamish
Andrabi, Ali
author_sort Soon, David SC
collection PubMed
description Mesothelial inclusion cyst is a rare benign tumour that has only 130 cases reported in the literature. Accurate diagnosis and optimal management of this condition remains uncertain. We report a 51-year-old African gentleman, whom presents with abdominal pain and constipation. A computed tomography scan was performed and revealed a large cystic lesion in the right paracolic gutter. The differential diagnosis included appendiceal mucinous neoplasm, cystic tuberculosis and duplication cyst. A laparotomy was performed due to his symptoms and size of the cyst. Macroscopically, the tumour had a size of 25 × 10 × 10 cm and revealed a necrotic lymph node. It was resected en bloc with the appendix and an ileocolic anastomosis performed. Histology revealed a diagnosis of mesothelial inclusion cyst and acute appendicitis. The patient recovered well and had no recurrence at 2-year follow-up.
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spelling pubmed-51650512016-12-20 Mesothelial inclusion cyst: a rare occurrence Soon, David SC Shilton, Hamish Andrabi, Ali J Surg Case Rep Case Report Mesothelial inclusion cyst is a rare benign tumour that has only 130 cases reported in the literature. Accurate diagnosis and optimal management of this condition remains uncertain. We report a 51-year-old African gentleman, whom presents with abdominal pain and constipation. A computed tomography scan was performed and revealed a large cystic lesion in the right paracolic gutter. The differential diagnosis included appendiceal mucinous neoplasm, cystic tuberculosis and duplication cyst. A laparotomy was performed due to his symptoms and size of the cyst. Macroscopically, the tumour had a size of 25 × 10 × 10 cm and revealed a necrotic lymph node. It was resected en bloc with the appendix and an ileocolic anastomosis performed. Histology revealed a diagnosis of mesothelial inclusion cyst and acute appendicitis. The patient recovered well and had no recurrence at 2-year follow-up. Oxford University Press 2016-12-19 /pmc/articles/PMC5165051/ /pubmed/27994008 http://dx.doi.org/10.1093/jscr/rjw213 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2016. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits noncommercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Soon, David SC
Shilton, Hamish
Andrabi, Ali
Mesothelial inclusion cyst: a rare occurrence
title Mesothelial inclusion cyst: a rare occurrence
title_full Mesothelial inclusion cyst: a rare occurrence
title_fullStr Mesothelial inclusion cyst: a rare occurrence
title_full_unstemmed Mesothelial inclusion cyst: a rare occurrence
title_short Mesothelial inclusion cyst: a rare occurrence
title_sort mesothelial inclusion cyst: a rare occurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5165051/
https://www.ncbi.nlm.nih.gov/pubmed/27994008
http://dx.doi.org/10.1093/jscr/rjw213
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