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Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report
BACKGROUND: Intrathoracic Solitary Fibrous Tumors (SFT) mainly arise from the pleura; however, these tumors may also originate from the mediastinum. We present a rare case of posterior SFT extending to several mediastinal sites and with an unusual large size, successfully treated with surgical resec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518089/ https://www.ncbi.nlm.nih.gov/pubmed/37742027 http://dx.doi.org/10.1186/s13019-023-02366-3 |
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author | Mardani, Parviz Nekooeian, Mohammad Zangeneh, Saba Kamran, Hooman Shahriarirad, Reza Anbardar, Mohammad Hossein Amirian, Armin Vafabin, Masoud |
author_facet | Mardani, Parviz Nekooeian, Mohammad Zangeneh, Saba Kamran, Hooman Shahriarirad, Reza Anbardar, Mohammad Hossein Amirian, Armin Vafabin, Masoud |
author_sort | Mardani, Parviz |
collection | PubMed |
description | BACKGROUND: Intrathoracic Solitary Fibrous Tumors (SFT) mainly arise from the pleura; however, these tumors may also originate from the mediastinum. We present a rare case of posterior SFT extending to several mediastinal sites and with an unusual large size, successfully treated with surgical resection. CASE PRESENTATION: A 66-year-old female presented with an initial manifestation of ambiguous pain in the chest and dysphagia and later developed pitting edema in both lower extremities and cachexia five months before admission. Chest imaging confirmed a mediastinal mass (17 × 15 × 8 cm) which was surgically removed. Immunohistochemistry confirmed the diagnosis of a solitary fibrous tumor with positive B-cell lymphoma 2, STAT6, and CD99, negative S100 and smooth muscle actin, and low levels of Ki67 (5–7%). The patient’s follow-up course was unremarkable. CONCLUSION: Mediastinal SFTs may grow extremely huge, with the potential to invade multiple adjacent sites. Surgical removal of the tumor remains the mainstay of treatment in these cases. |
format | Online Article Text |
id | pubmed-10518089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105180892023-09-25 Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report Mardani, Parviz Nekooeian, Mohammad Zangeneh, Saba Kamran, Hooman Shahriarirad, Reza Anbardar, Mohammad Hossein Amirian, Armin Vafabin, Masoud J Cardiothorac Surg Case Report BACKGROUND: Intrathoracic Solitary Fibrous Tumors (SFT) mainly arise from the pleura; however, these tumors may also originate from the mediastinum. We present a rare case of posterior SFT extending to several mediastinal sites and with an unusual large size, successfully treated with surgical resection. CASE PRESENTATION: A 66-year-old female presented with an initial manifestation of ambiguous pain in the chest and dysphagia and later developed pitting edema in both lower extremities and cachexia five months before admission. Chest imaging confirmed a mediastinal mass (17 × 15 × 8 cm) which was surgically removed. Immunohistochemistry confirmed the diagnosis of a solitary fibrous tumor with positive B-cell lymphoma 2, STAT6, and CD99, negative S100 and smooth muscle actin, and low levels of Ki67 (5–7%). The patient’s follow-up course was unremarkable. CONCLUSION: Mediastinal SFTs may grow extremely huge, with the potential to invade multiple adjacent sites. Surgical removal of the tumor remains the mainstay of treatment in these cases. BioMed Central 2023-09-23 /pmc/articles/PMC10518089/ /pubmed/37742027 http://dx.doi.org/10.1186/s13019-023-02366-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Mardani, Parviz Nekooeian, Mohammad Zangeneh, Saba Kamran, Hooman Shahriarirad, Reza Anbardar, Mohammad Hossein Amirian, Armin Vafabin, Masoud Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title | Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title_full | Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title_fullStr | Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title_full_unstemmed | Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title_short | Surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
title_sort | surgical removal of an unusual huge solitary fibrous tumor in the mediastinum: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518089/ https://www.ncbi.nlm.nih.gov/pubmed/37742027 http://dx.doi.org/10.1186/s13019-023-02366-3 |
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