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An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report

BACKGROUND: Mediastinal mass management may represent a real challenge for all the physicians who deal with it. Mediastinum, in fact, contains different vital structures which are often involved by growing neoplasms with increasing severity. Therefore, up to 60% of the patients with mediastinal mass...

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Autores principales: Sicolo, Elisa, Aprile, Vittorio, Ferrarello, Tommaso, Bacchin, Diana, Mastromarino, Maria Giovanna, Alì, Greta, Ambrogi, Marcello Carlo, Lucchi, Marco, Korasidis, Stylianos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792865/
https://www.ncbi.nlm.nih.gov/pubmed/36582979
http://dx.doi.org/10.21037/med-22-8
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author Sicolo, Elisa
Aprile, Vittorio
Ferrarello, Tommaso
Bacchin, Diana
Mastromarino, Maria Giovanna
Alì, Greta
Ambrogi, Marcello Carlo
Lucchi, Marco
Korasidis, Stylianos
author_facet Sicolo, Elisa
Aprile, Vittorio
Ferrarello, Tommaso
Bacchin, Diana
Mastromarino, Maria Giovanna
Alì, Greta
Ambrogi, Marcello Carlo
Lucchi, Marco
Korasidis, Stylianos
author_sort Sicolo, Elisa
collection PubMed
description BACKGROUND: Mediastinal mass management may represent a real challenge for all the physicians who deal with it. Mediastinum, in fact, contains different vital structures which are often involved by growing neoplasms with increasing severity. Therefore, up to 60% of the patients with mediastinal mass are symptomatic, according to the structure involved. Different neoplasms may arise essentially from all mediastinal organs, whereas thymic epithelial tumors and lymphomas represent more than 90% of mediastinal tumors. CASE DESCRIPTION: We report the first case described of a giant asymptomatic mediastinal mass in a 43-year-old male affected by Down syndrome (DS), turned out to be a thymoma, treated exclusively and successfully with radical surgery. Despite the absence of any symptoms, the giant thymoma infiltrated the diaphragm, the pericardium, the upper lobe of the left lung together with the left phrenic nerve resulting in the compression of heart and great vessels. CONCLUSIONS: To date, this is the first description of a thymic malignancy in a patient with DS, that usually is characterized by a low-incidence of solid tumor except for germ-cells ones. Surgery has been extremely challenging, due the clinical condition of the patient together with the tumor features; nevertheless, oncological radicality criteria were completely fulfilled. After four years from surgery, the patient is alive and still disease-free, highlighting the importance of radical surgery.
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spelling pubmed-97928652022-12-28 An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report Sicolo, Elisa Aprile, Vittorio Ferrarello, Tommaso Bacchin, Diana Mastromarino, Maria Giovanna Alì, Greta Ambrogi, Marcello Carlo Lucchi, Marco Korasidis, Stylianos Mediastinum Case Report BACKGROUND: Mediastinal mass management may represent a real challenge for all the physicians who deal with it. Mediastinum, in fact, contains different vital structures which are often involved by growing neoplasms with increasing severity. Therefore, up to 60% of the patients with mediastinal mass are symptomatic, according to the structure involved. Different neoplasms may arise essentially from all mediastinal organs, whereas thymic epithelial tumors and lymphomas represent more than 90% of mediastinal tumors. CASE DESCRIPTION: We report the first case described of a giant asymptomatic mediastinal mass in a 43-year-old male affected by Down syndrome (DS), turned out to be a thymoma, treated exclusively and successfully with radical surgery. Despite the absence of any symptoms, the giant thymoma infiltrated the diaphragm, the pericardium, the upper lobe of the left lung together with the left phrenic nerve resulting in the compression of heart and great vessels. CONCLUSIONS: To date, this is the first description of a thymic malignancy in a patient with DS, that usually is characterized by a low-incidence of solid tumor except for germ-cells ones. Surgery has been extremely challenging, due the clinical condition of the patient together with the tumor features; nevertheless, oncological radicality criteria were completely fulfilled. After four years from surgery, the patient is alive and still disease-free, highlighting the importance of radical surgery. AME Publishing Company 2022-12-25 /pmc/articles/PMC9792865/ /pubmed/36582979 http://dx.doi.org/10.21037/med-22-8 Text en 2022 Mediastinum. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Sicolo, Elisa
Aprile, Vittorio
Ferrarello, Tommaso
Bacchin, Diana
Mastromarino, Maria Giovanna
Alì, Greta
Ambrogi, Marcello Carlo
Lucchi, Marco
Korasidis, Stylianos
An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title_full An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title_fullStr An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title_full_unstemmed An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title_short An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report
title_sort asymptomatic giant ab thymoma in a patient with down syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792865/
https://www.ncbi.nlm.nih.gov/pubmed/36582979
http://dx.doi.org/10.21037/med-22-8
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