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Neuroendocrine carcinoma arising in a tailgut cyst
INTRODUCTION: A tailgut cyst, also called retrorectal cystic hamartoma, is a rare congenital lesion that forms most commonly in the retrorectal space. It is presumed to arise from remnants of early embryogenesis. PRESENTATION OF CASE: The following report describes a unique case of a retrorectal cys...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039892/ https://www.ncbi.nlm.nih.gov/pubmed/29966957 http://dx.doi.org/10.1016/j.ijscr.2018.05.032 |
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author | Al Khaldi, Maher Mesbah, Amanda Dubé, Pierre Isler, Marc Mitchell, Andrew Doyon, Josée Sideris, Lucas |
author_facet | Al Khaldi, Maher Mesbah, Amanda Dubé, Pierre Isler, Marc Mitchell, Andrew Doyon, Josée Sideris, Lucas |
author_sort | Al Khaldi, Maher |
collection | PubMed |
description | INTRODUCTION: A tailgut cyst, also called retrorectal cystic hamartoma, is a rare congenital lesion that forms most commonly in the retrorectal space. It is presumed to arise from remnants of early embryogenesis. PRESENTATION OF CASE: The following report describes a unique case of a retrorectal cystic hamartoma in a 53 year-old French Canadian man with a history of low back pain. The tumour underwent malignant transformation into a well-differentiated neuroendocrine carcinoma three years after the beginning of symptoms. DISCUSSION: This condition can be found at any age, but occurs especially among middle-aged women. Not only is it frequently misdiagnosed, but also several complications associated to the cyst have been reported such as infection and malignant transformation. This is why complete surgical excision of the tailgut cyst is currently recommended. |
format | Online Article Text |
id | pubmed-6039892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60398922018-07-12 Neuroendocrine carcinoma arising in a tailgut cyst Al Khaldi, Maher Mesbah, Amanda Dubé, Pierre Isler, Marc Mitchell, Andrew Doyon, Josée Sideris, Lucas Int J Surg Case Rep Article INTRODUCTION: A tailgut cyst, also called retrorectal cystic hamartoma, is a rare congenital lesion that forms most commonly in the retrorectal space. It is presumed to arise from remnants of early embryogenesis. PRESENTATION OF CASE: The following report describes a unique case of a retrorectal cystic hamartoma in a 53 year-old French Canadian man with a history of low back pain. The tumour underwent malignant transformation into a well-differentiated neuroendocrine carcinoma three years after the beginning of symptoms. DISCUSSION: This condition can be found at any age, but occurs especially among middle-aged women. Not only is it frequently misdiagnosed, but also several complications associated to the cyst have been reported such as infection and malignant transformation. This is why complete surgical excision of the tailgut cyst is currently recommended. Elsevier 2018-06-28 /pmc/articles/PMC6039892/ /pubmed/29966957 http://dx.doi.org/10.1016/j.ijscr.2018.05.032 Text en © 2018 The Author(s) 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 | Article Al Khaldi, Maher Mesbah, Amanda Dubé, Pierre Isler, Marc Mitchell, Andrew Doyon, Josée Sideris, Lucas Neuroendocrine carcinoma arising in a tailgut cyst |
title | Neuroendocrine carcinoma arising in a tailgut cyst |
title_full | Neuroendocrine carcinoma arising in a tailgut cyst |
title_fullStr | Neuroendocrine carcinoma arising in a tailgut cyst |
title_full_unstemmed | Neuroendocrine carcinoma arising in a tailgut cyst |
title_short | Neuroendocrine carcinoma arising in a tailgut cyst |
title_sort | neuroendocrine carcinoma arising in a tailgut cyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039892/ https://www.ncbi.nlm.nih.gov/pubmed/29966957 http://dx.doi.org/10.1016/j.ijscr.2018.05.032 |
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