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An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report
RATIONALE: Giant fibrovascular polyps (GFVPs) found in the hypopharynx are exceedingly rare. These are benign tumors which are identified by CT or MRI and usually treated based on symptoms. Even more rarely, pathology may identify one of these masses as an atypical lipomatous tumor (ALT). This paper...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671807/ https://www.ncbi.nlm.nih.gov/pubmed/29068974 http://dx.doi.org/10.1097/MD.0000000000006927 |
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author | Ioanidis, Khrystyna E. MacNeil, Stephanie Danielle Tay, Keng Yeow Wehrli, Bret |
author_facet | Ioanidis, Khrystyna E. MacNeil, Stephanie Danielle Tay, Keng Yeow Wehrli, Bret |
author_sort | Ioanidis, Khrystyna E. |
collection | PubMed |
description | RATIONALE: Giant fibrovascular polyps (GFVPs) found in the hypopharynx are exceedingly rare. These are benign tumors which are identified by CT or MRI and usually treated based on symptoms. Even more rarely, pathology may identify one of these masses as an atypical lipomatous tumor (ALT). This paper will present a case of an ALT of the hypopharynx that was originally classified as a GFVP, highlighting the difficulty in distinguishing between them and the importance of making the correct diagnosis. PATIENT CONCERNS: An 84-year-old man presented to the emergency department with a 6-month history of a pedunculated hypopharyngeal growth, dysphagia, and intermittent dyspnea. DIAGNOSES: The mass was characterized as a GFVP by barium swallow and MRI. INTERVENTIONS: The hypopharyngeal mass was resected for obstructive symptoms and to confirm the diagnosis. Final pathology found the mass to be more consistent with an atypical lipomatous tumor (ALT). OUTCOMES: The patient's dysphagia and dyspnea resolved. He was free of recurrence at 22 months postoperative. LESSONS: Both GFVPs and ALTs are very rarely found in the hypopharynx but can be easily misclassified as one another. Imaging is useful to initially characterize the mass, but to definitively differentiate between them, pathological analysis is necessary. Although they are rare, it is important to consider both possibilities on the differential for hypopharyngeal masses. Further, accurate analysis is essential to distinguish between them because their definitive management and follow-up is different. |
format | Online Article Text |
id | pubmed-5671807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-56718072017-11-22 An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report Ioanidis, Khrystyna E. MacNeil, Stephanie Danielle Tay, Keng Yeow Wehrli, Bret Medicine (Baltimore) 6000 RATIONALE: Giant fibrovascular polyps (GFVPs) found in the hypopharynx are exceedingly rare. These are benign tumors which are identified by CT or MRI and usually treated based on symptoms. Even more rarely, pathology may identify one of these masses as an atypical lipomatous tumor (ALT). This paper will present a case of an ALT of the hypopharynx that was originally classified as a GFVP, highlighting the difficulty in distinguishing between them and the importance of making the correct diagnosis. PATIENT CONCERNS: An 84-year-old man presented to the emergency department with a 6-month history of a pedunculated hypopharyngeal growth, dysphagia, and intermittent dyspnea. DIAGNOSES: The mass was characterized as a GFVP by barium swallow and MRI. INTERVENTIONS: The hypopharyngeal mass was resected for obstructive symptoms and to confirm the diagnosis. Final pathology found the mass to be more consistent with an atypical lipomatous tumor (ALT). OUTCOMES: The patient's dysphagia and dyspnea resolved. He was free of recurrence at 22 months postoperative. LESSONS: Both GFVPs and ALTs are very rarely found in the hypopharynx but can be easily misclassified as one another. Imaging is useful to initially characterize the mass, but to definitively differentiate between them, pathological analysis is necessary. Although they are rare, it is important to consider both possibilities on the differential for hypopharyngeal masses. Further, accurate analysis is essential to distinguish between them because their definitive management and follow-up is different. Wolters Kluwer Health 2017-10-27 /pmc/articles/PMC5671807/ /pubmed/29068974 http://dx.doi.org/10.1097/MD.0000000000006927 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 6000 Ioanidis, Khrystyna E. MacNeil, Stephanie Danielle Tay, Keng Yeow Wehrli, Bret An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title | An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title_full | An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title_fullStr | An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title_full_unstemmed | An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title_short | An atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: A case report |
title_sort | atypical lipomatous tumor mimicking a giant fibrovascular polyp of the hypopharynx: a case report |
topic | 6000 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671807/ https://www.ncbi.nlm.nih.gov/pubmed/29068974 http://dx.doi.org/10.1097/MD.0000000000006927 |
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