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Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy

We report a case of inadvertent hoarseness after surgery for primary pulmonary amyloidosis. A 55-year-old male was transferred to our facility due to a lung mass. Chest computed tomography revealed a solitary pulmonary nodule. Positron emission tomography–computed tomography showed fluorodeoxyglucos...

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Autores principales: Kim, Dohun, Lee, Yong-Moon, Kim, Si-Wook, Kim, Jong-Won, Hong, Jong-Myeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900869/
https://www.ncbi.nlm.nih.gov/pubmed/27298804
http://dx.doi.org/10.5090/kjtcs.2016.49.3.218
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author Kim, Dohun
Lee, Yong-Moon
Kim, Si-Wook
Kim, Jong-Won
Hong, Jong-Myeon
author_facet Kim, Dohun
Lee, Yong-Moon
Kim, Si-Wook
Kim, Jong-Won
Hong, Jong-Myeon
author_sort Kim, Dohun
collection PubMed
description We report a case of inadvertent hoarseness after surgery for primary pulmonary amyloidosis. A 55-year-old male was transferred to our facility due to a lung mass. Chest computed tomography revealed a solitary pulmonary nodule. Positron emission tomography–computed tomography showed fluorodeoxyglucose uptake in the main mass and in the mediastinal lymph nodes. To confirm the pathology of the mass, wedge resection and thorough lymph node dissection were performed via video-assisted thoracic surgery (VATS). No complications except for hoarseness were observed; hoarseness developed soon after surgery and lasted for 3 months. The main mass was diagnosed as amyloidosis, but this was not found in the lymph nodes. In conclusion, VATS wedge resection for peripheral amyloidosis is a feasible and safe procedure. However, mediastinal lymph node dissection is not recommended unless there is evidence of a clear benefit.
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spelling pubmed-49008692016-06-13 Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy Kim, Dohun Lee, Yong-Moon Kim, Si-Wook Kim, Jong-Won Hong, Jong-Myeon Korean J Thorac Cardiovasc Surg Case Report We report a case of inadvertent hoarseness after surgery for primary pulmonary amyloidosis. A 55-year-old male was transferred to our facility due to a lung mass. Chest computed tomography revealed a solitary pulmonary nodule. Positron emission tomography–computed tomography showed fluorodeoxyglucose uptake in the main mass and in the mediastinal lymph nodes. To confirm the pathology of the mass, wedge resection and thorough lymph node dissection were performed via video-assisted thoracic surgery (VATS). No complications except for hoarseness were observed; hoarseness developed soon after surgery and lasted for 3 months. The main mass was diagnosed as amyloidosis, but this was not found in the lymph nodes. In conclusion, VATS wedge resection for peripheral amyloidosis is a feasible and safe procedure. However, mediastinal lymph node dissection is not recommended unless there is evidence of a clear benefit. The Korean Society for Thoracic and Cardiovascular Surgery 2016-06 2016-06-05 /pmc/articles/PMC4900869/ /pubmed/27298804 http://dx.doi.org/10.5090/kjtcs.2016.49.3.218 Text en Copyright © 2016 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Dohun
Lee, Yong-Moon
Kim, Si-Wook
Kim, Jong-Won
Hong, Jong-Myeon
Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title_full Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title_fullStr Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title_full_unstemmed Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title_short Primary Pulmonary Amyloidosis with Mediastinal Lymphadenopathy
title_sort primary pulmonary amyloidosis with mediastinal lymphadenopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900869/
https://www.ncbi.nlm.nih.gov/pubmed/27298804
http://dx.doi.org/10.5090/kjtcs.2016.49.3.218
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