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Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction
Primary synovial sarcoma is a soft tissue tumor which originates from synovial‐like undeveloped mesenchymal structures. Here, we report the case of a giant mediastinal sarcoma in a 41‐year‐old female patient. After diagnosis, she underwent neoadjuvant chemotherapy. Due to its low efficacy, we colleg...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262890/ https://www.ncbi.nlm.nih.gov/pubmed/32329211 http://dx.doi.org/10.1111/1759-7714.13452 |
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author | Frasca, Luca Longo, Filippo Tacchi, Giovanni Stilo, Francesco Zito, Anna Brunetti, Beniamino Depalma, Massimiliano Crucitti, Pierfilippo |
author_facet | Frasca, Luca Longo, Filippo Tacchi, Giovanni Stilo, Francesco Zito, Anna Brunetti, Beniamino Depalma, Massimiliano Crucitti, Pierfilippo |
author_sort | Frasca, Luca |
collection | PubMed |
description | Primary synovial sarcoma is a soft tissue tumor which originates from synovial‐like undeveloped mesenchymal structures. Here, we report the case of a giant mediastinal sarcoma in a 41‐year‐old female patient. After diagnosis, she underwent neoadjuvant chemotherapy. Due to its low efficacy, we collegially decided to undergo cytoreductive debulking surgery. The mass invaded the phrenic nerve bilaterally and its excision caused a severe lesion of the left nerve and a partial impairment of the right one. Thus, plastic surgeons decided to reconstruct the right phrenic nerve employing the contralateral remaining fibers. The invasiveness of this tumor, its difficult removal, histological profile and the peculiar technique to preserve diaphragmatic function classify this case as very rare. The therapeutic strategy was based on interdisciplinary teamwork which comprised several specialists' opinions. Our strategy allowed us to pursue the challenging objective to give a young woman with a severe diagnosis the best possible chance of achieving a good quality of life. To the best of our knowledge, this phrenic nerve reconstructive technique is very rare and has not previously been reported in the literature. The report emphasizes that it is possible to deal with an apparently impossible case through a collaborative approach involving several different medical specialist professionals. |
format | Online Article Text |
id | pubmed-7262890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72628902020-06-01 Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction Frasca, Luca Longo, Filippo Tacchi, Giovanni Stilo, Francesco Zito, Anna Brunetti, Beniamino Depalma, Massimiliano Crucitti, Pierfilippo Thorac Cancer Case Reports Primary synovial sarcoma is a soft tissue tumor which originates from synovial‐like undeveloped mesenchymal structures. Here, we report the case of a giant mediastinal sarcoma in a 41‐year‐old female patient. After diagnosis, she underwent neoadjuvant chemotherapy. Due to its low efficacy, we collegially decided to undergo cytoreductive debulking surgery. The mass invaded the phrenic nerve bilaterally and its excision caused a severe lesion of the left nerve and a partial impairment of the right one. Thus, plastic surgeons decided to reconstruct the right phrenic nerve employing the contralateral remaining fibers. The invasiveness of this tumor, its difficult removal, histological profile and the peculiar technique to preserve diaphragmatic function classify this case as very rare. The therapeutic strategy was based on interdisciplinary teamwork which comprised several specialists' opinions. Our strategy allowed us to pursue the challenging objective to give a young woman with a severe diagnosis the best possible chance of achieving a good quality of life. To the best of our knowledge, this phrenic nerve reconstructive technique is very rare and has not previously been reported in the literature. The report emphasizes that it is possible to deal with an apparently impossible case through a collaborative approach involving several different medical specialist professionals. John Wiley & Sons Australia, Ltd 2020-04-23 2020-06 /pmc/articles/PMC7262890/ /pubmed/32329211 http://dx.doi.org/10.1111/1759-7714.13452 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Frasca, Luca Longo, Filippo Tacchi, Giovanni Stilo, Francesco Zito, Anna Brunetti, Beniamino Depalma, Massimiliano Crucitti, Pierfilippo Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title | Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title_full | Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title_fullStr | Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title_full_unstemmed | Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title_short | Importance of muldisciplinary management of giant mediastinal sarcoma: A case report with phrenic nerve reconstruction |
title_sort | importance of muldisciplinary management of giant mediastinal sarcoma: a case report with phrenic nerve reconstruction |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262890/ https://www.ncbi.nlm.nih.gov/pubmed/32329211 http://dx.doi.org/10.1111/1759-7714.13452 |
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