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Mucinous adenocarcinoma arising from a tailgut cyst: A case report
BACKGROUND: Retrorectal hamartomas or tailgut cysts (TCs) are rare. In most cases, they are asymptomatic and benign; however, rarely, they undergo malignant transformation, mainly in the form of adenocarcinoma. CASE SUMMARY: A 55-year-old woman presented to our hospital with lower back pain. On magn...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630997/ https://www.ncbi.nlm.nih.gov/pubmed/36337315 http://dx.doi.org/10.5306/wjco.v13.i10.853 |
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author | Malliou, Petra Syrnioti, Antonia Koletsa, Triantafyllia Karlafti, Eleni Karakatsanis, Anestis Raptou, Georgia Apostolidis, Stylianos Michalopoulos, Antonios Paramythiotis, Daniel |
author_facet | Malliou, Petra Syrnioti, Antonia Koletsa, Triantafyllia Karlafti, Eleni Karakatsanis, Anestis Raptou, Georgia Apostolidis, Stylianos Michalopoulos, Antonios Paramythiotis, Daniel |
author_sort | Malliou, Petra |
collection | PubMed |
description | BACKGROUND: Retrorectal hamartomas or tailgut cysts (TCs) are rare. In most cases, they are asymptomatic and benign; however, rarely, they undergo malignant transformation, mainly in the form of adenocarcinoma. CASE SUMMARY: A 55-year-old woman presented to our hospital with lower back pain. On magnetic resonance imaging, a large pelvic mass was found, which was located on the right of the ischiorectal fossa, extending to the minor pelvis. The patient underwent extensive surgical resection of the lesion through the right buttock. Histological examination confirmed the diagnosis of a retrorectal mucinous adenocarcinoma originating from a TC. Surgical resection of the tumour was complete, and the patient recovered without complications. The pilonidal sinus was then excised. One year later, semi-annual positron emission tomography-computed tomography and magnetic resonance imaging scans did not reveal any evidence of local recurrence or metastatic disease. CONCLUSION: Preoperative recognition, histological diagnosis, and treatment of TCs pose significant challenges. In addition, the possibility of developing invasive mucinous adenocarcinoma, although rare, should be considered. |
format | Online Article Text |
id | pubmed-9630997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-96309972022-11-04 Mucinous adenocarcinoma arising from a tailgut cyst: A case report Malliou, Petra Syrnioti, Antonia Koletsa, Triantafyllia Karlafti, Eleni Karakatsanis, Anestis Raptou, Georgia Apostolidis, Stylianos Michalopoulos, Antonios Paramythiotis, Daniel World J Clin Oncol Case Report BACKGROUND: Retrorectal hamartomas or tailgut cysts (TCs) are rare. In most cases, they are asymptomatic and benign; however, rarely, they undergo malignant transformation, mainly in the form of adenocarcinoma. CASE SUMMARY: A 55-year-old woman presented to our hospital with lower back pain. On magnetic resonance imaging, a large pelvic mass was found, which was located on the right of the ischiorectal fossa, extending to the minor pelvis. The patient underwent extensive surgical resection of the lesion through the right buttock. Histological examination confirmed the diagnosis of a retrorectal mucinous adenocarcinoma originating from a TC. Surgical resection of the tumour was complete, and the patient recovered without complications. The pilonidal sinus was then excised. One year later, semi-annual positron emission tomography-computed tomography and magnetic resonance imaging scans did not reveal any evidence of local recurrence or metastatic disease. CONCLUSION: Preoperative recognition, histological diagnosis, and treatment of TCs pose significant challenges. In addition, the possibility of developing invasive mucinous adenocarcinoma, although rare, should be considered. Baishideng Publishing Group Inc 2022-10-24 2022-10-24 /pmc/articles/PMC9630997/ /pubmed/36337315 http://dx.doi.org/10.5306/wjco.v13.i10.853 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Malliou, Petra Syrnioti, Antonia Koletsa, Triantafyllia Karlafti, Eleni Karakatsanis, Anestis Raptou, Georgia Apostolidis, Stylianos Michalopoulos, Antonios Paramythiotis, Daniel Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title | Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title_full | Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title_fullStr | Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title_full_unstemmed | Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title_short | Mucinous adenocarcinoma arising from a tailgut cyst: A case report |
title_sort | mucinous adenocarcinoma arising from a tailgut cyst: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630997/ https://www.ncbi.nlm.nih.gov/pubmed/36337315 http://dx.doi.org/10.5306/wjco.v13.i10.853 |
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