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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...

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Autores principales: Mardani, Parviz, Nekooeian, Mohammad, Zangeneh, Saba, Kamran, Hooman, Shahriarirad, Reza, Anbardar, Mohammad Hossein, Amirian, Armin, Vafabin, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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.
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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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