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Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review

BACKGROUND: Solitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor that arises at various sites and typically originates from the pleura. Most patients with SFTPs are asymptomatic, unless the tumor is large. Approximately 20% of SFTP cases are malignant. There are few reports on ima...

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Autores principales: Yao, Kelin, Zhu, Lvcong, Wang, Liang, Xia, Ruiming, Yang, Jianfeng, Hu, Wenbin, Yu, Zhongqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9158379/
https://www.ncbi.nlm.nih.gov/pubmed/35641960
http://dx.doi.org/10.1186/s13019-022-01881-z
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author Yao, Kelin
Zhu, Lvcong
Wang, Liang
Xia, Ruiming
Yang, Jianfeng
Hu, Wenbin
Yu, Zhongqiang
author_facet Yao, Kelin
Zhu, Lvcong
Wang, Liang
Xia, Ruiming
Yang, Jianfeng
Hu, Wenbin
Yu, Zhongqiang
author_sort Yao, Kelin
collection PubMed
description BACKGROUND: Solitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor that arises at various sites and typically originates from the pleura. Most patients with SFTPs are asymptomatic, unless the tumor is large. Approximately 20% of SFTP cases are malignant. There are few reports on imaging diagnoses and interventional treatments of SFTP. Here, we report a case of a giant SFTP that exhibited malignant behavior and underwent successful resection after embolization of the main supply artery of the tumor. CASE PRESENTATION: We report a clinical case of a giant SFTP in a 66-year-old Chinese female patient complaining of chest tightness and cough for more than 2 months. Ten years ago, the patient had undergone a chest CT scan at a local hospital for cough. Computed tomography (CT) had revealed a mass in the right thoracic region, which was misdiagnosed as a pulmonary abscess by CT-guided biopsy. Therefore, the patient did not receive appropriate/complete treatment at that time. She was hospitalized again, because CT showed significant enlargement of the right thoracic mass, which caused her obvious symptoms of discomfort. The pathological results of CT-guided biopsy at our hospital confirmed SFTP. Considering the large size of the tumor and the rich blood supply, some of the main blood vessels were treated with embolization before surgical resection. A large tumor, about 23 cm × 16 cm × 15 cm in size, was then successfully removed by thoracic surgery. The diagnosis of malignant SFTP was confirmed by surgical pathology and immunohistochemistry. CONCLUSION: Imaging findings of SFTPs are not characteristic, especially when a tumor is large, the diagnosis is difficult, and the final diagnosis still depends on histological and immunohistochemical examinations. The two-stage surgical treatment described here, which involves first embolization of the main supplying artery of the large tumor and then complete surgical resection, is effective and safe for SFTPs. Whether needle biopsy or vascular embolization is performed, intervention plays a crucial role in the diagnosis and treatment of patients with SFTPs.
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spelling pubmed-91583792022-06-02 Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review Yao, Kelin Zhu, Lvcong Wang, Liang Xia, Ruiming Yang, Jianfeng Hu, Wenbin Yu, Zhongqiang J Cardiothorac Surg Case Report BACKGROUND: Solitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor that arises at various sites and typically originates from the pleura. Most patients with SFTPs are asymptomatic, unless the tumor is large. Approximately 20% of SFTP cases are malignant. There are few reports on imaging diagnoses and interventional treatments of SFTP. Here, we report a case of a giant SFTP that exhibited malignant behavior and underwent successful resection after embolization of the main supply artery of the tumor. CASE PRESENTATION: We report a clinical case of a giant SFTP in a 66-year-old Chinese female patient complaining of chest tightness and cough for more than 2 months. Ten years ago, the patient had undergone a chest CT scan at a local hospital for cough. Computed tomography (CT) had revealed a mass in the right thoracic region, which was misdiagnosed as a pulmonary abscess by CT-guided biopsy. Therefore, the patient did not receive appropriate/complete treatment at that time. She was hospitalized again, because CT showed significant enlargement of the right thoracic mass, which caused her obvious symptoms of discomfort. The pathological results of CT-guided biopsy at our hospital confirmed SFTP. Considering the large size of the tumor and the rich blood supply, some of the main blood vessels were treated with embolization before surgical resection. A large tumor, about 23 cm × 16 cm × 15 cm in size, was then successfully removed by thoracic surgery. The diagnosis of malignant SFTP was confirmed by surgical pathology and immunohistochemistry. CONCLUSION: Imaging findings of SFTPs are not characteristic, especially when a tumor is large, the diagnosis is difficult, and the final diagnosis still depends on histological and immunohistochemical examinations. The two-stage surgical treatment described here, which involves first embolization of the main supplying artery of the large tumor and then complete surgical resection, is effective and safe for SFTPs. Whether needle biopsy or vascular embolization is performed, intervention plays a crucial role in the diagnosis and treatment of patients with SFTPs. BioMed Central 2022-05-31 /pmc/articles/PMC9158379/ /pubmed/35641960 http://dx.doi.org/10.1186/s13019-022-01881-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Yao, Kelin
Zhu, Lvcong
Wang, Liang
Xia, Ruiming
Yang, Jianfeng
Hu, Wenbin
Yu, Zhongqiang
Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title_full Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title_fullStr Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title_full_unstemmed Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title_short Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
title_sort resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9158379/
https://www.ncbi.nlm.nih.gov/pubmed/35641960
http://dx.doi.org/10.1186/s13019-022-01881-z
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