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Synovial sarcoma leading to a paraesophageal abscess in a child

BACKGROUND: Synovial sarcoma (SS) is an uncommon malignant neoplasm arising from primitive pluripotential mesenchyme primarily affecting the soft tissues of the extremities. Rarely other locations are involved, including the mediastinum. CASE REPORT: After treatment for mediastinal SS by surgical re...

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Autores principales: Keeling, Lisa, Gordon, Catherine, Sawaya, David, Giles, Henry, Nowicki, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616142/
https://www.ncbi.nlm.nih.gov/pubmed/23569508
http://dx.doi.org/10.12659/AJCR.883234
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author Keeling, Lisa
Gordon, Catherine
Sawaya, David
Giles, Henry
Nowicki, Michael
author_facet Keeling, Lisa
Gordon, Catherine
Sawaya, David
Giles, Henry
Nowicki, Michael
author_sort Keeling, Lisa
collection PubMed
description BACKGROUND: Synovial sarcoma (SS) is an uncommon malignant neoplasm arising from primitive pluripotential mesenchyme primarily affecting the soft tissues of the extremities. Rarely other locations are involved, including the mediastinum. CASE REPORT: After treatment for mediastinal SS by surgical resection, radiation therapy, and chemotherapy, an 11-year-old boy developed an esophageal stricture and fistula, the latter resulting in a paraesophageal abscess. Management of the esophageal stricture and fistula required a multi-disciplinary approach. We report our experience with the management of this difficult complication, as well as a brief review of the literature on SS. CONCLUSIONS: Rare conditions, particularly those with unusual complications, present therapeutic challenges requiring a multi-disciplinary team approach. Reporting experiences with difficult cases can benefit providers faced with similar problems in the future.
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spelling pubmed-36161422013-04-08 Synovial sarcoma leading to a paraesophageal abscess in a child Keeling, Lisa Gordon, Catherine Sawaya, David Giles, Henry Nowicki, Michael Am J Case Rep Case Report BACKGROUND: Synovial sarcoma (SS) is an uncommon malignant neoplasm arising from primitive pluripotential mesenchyme primarily affecting the soft tissues of the extremities. Rarely other locations are involved, including the mediastinum. CASE REPORT: After treatment for mediastinal SS by surgical resection, radiation therapy, and chemotherapy, an 11-year-old boy developed an esophageal stricture and fistula, the latter resulting in a paraesophageal abscess. Management of the esophageal stricture and fistula required a multi-disciplinary approach. We report our experience with the management of this difficult complication, as well as a brief review of the literature on SS. CONCLUSIONS: Rare conditions, particularly those with unusual complications, present therapeutic challenges requiring a multi-disciplinary team approach. Reporting experiences with difficult cases can benefit providers faced with similar problems in the future. International Scientific Literature, Inc. 2012-06-29 /pmc/articles/PMC3616142/ /pubmed/23569508 http://dx.doi.org/10.12659/AJCR.883234 Text en © Am J Case Rep, 2012 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
spellingShingle Case Report
Keeling, Lisa
Gordon, Catherine
Sawaya, David
Giles, Henry
Nowicki, Michael
Synovial sarcoma leading to a paraesophageal abscess in a child
title Synovial sarcoma leading to a paraesophageal abscess in a child
title_full Synovial sarcoma leading to a paraesophageal abscess in a child
title_fullStr Synovial sarcoma leading to a paraesophageal abscess in a child
title_full_unstemmed Synovial sarcoma leading to a paraesophageal abscess in a child
title_short Synovial sarcoma leading to a paraesophageal abscess in a child
title_sort synovial sarcoma leading to a paraesophageal abscess in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616142/
https://www.ncbi.nlm.nih.gov/pubmed/23569508
http://dx.doi.org/10.12659/AJCR.883234
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