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Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review
BACKGROUND: Azygos vein aneurysms (AVAs) are extremely rare. The majority of patients have no obvious clinical symptoms, so they are found by physical examination or by chance. There is limited clinical treatment experience that can be referred to, and there are no clear guidelines or research evide...
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/PMC9844024/ https://www.ncbi.nlm.nih.gov/pubmed/36647165 http://dx.doi.org/10.1186/s13019-023-02143-2 |
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author | Yao, Yi Hu, Qiuxia Xie, Xiaoyang Liu, Caiyang Lei, Yu Li, Xiaoliang Wang, Yi Liu, Gaohua Yang, Yanhui Luo, Lei Li, Ji |
author_facet | Yao, Yi Hu, Qiuxia Xie, Xiaoyang Liu, Caiyang Lei, Yu Li, Xiaoliang Wang, Yi Liu, Gaohua Yang, Yanhui Luo, Lei Li, Ji |
author_sort | Yao, Yi |
collection | PubMed |
description | BACKGROUND: Azygos vein aneurysms (AVAs) are extremely rare. The majority of patients have no obvious clinical symptoms, so they are found by physical examination or by chance. There is limited clinical treatment experience that can be referred to, and there are no clear guidelines or research evidence standardizing the surgical and interventional therapy. Here, we report a patient with idiopathic AVA whose three-dimensional reconstruction of the tumor was completed before surgery. On the basis of three-dimensional reconstruction, single-port thoracoscopic resection of the AVA was successfully completed and reported for the first time. The previously reported cases are summarized to provide guidance for the diagnosis and treatment of patients with AVAs. CASE PRESENTATION: A 56-year-old man was transferred to our hospital due to “dysphagia”. The diagnosis of AVA was made after enhanced computed tomography, gastroscopy, fiberoptic bronchoscopy, and three-dimensional reconstruction. Congenital weakness or degenerative changes causes the vein walls to be extremely thin that the AVA had the risk of ruptur. Furthermore, the patient had symptoms of dysphagia, he received single-port thoracoscopic surgery. After the operation, his dysphagia disappeared. The postoperative pathology confirmed hemangioma. The patient was discharged 3 days after surgery without any complications. CONCLUSIONS: AVAs are rare. Preoperative three-dimensional reconstruction can greatly help surgeons clarify the disease diagnosis, formulate the surgical plan, avoid damage to the surrounding vital organs, and reduce intraoperative bleeding. Thoracoscopic surgery to remove AVAs is difficult and has a high risk of bleeding, while more minimally invasive single-port thoracoscopic surgery is also safe and effective for the treatment of AVAs. |
format | Online Article Text |
id | pubmed-9844024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98440242023-01-18 Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review Yao, Yi Hu, Qiuxia Xie, Xiaoyang Liu, Caiyang Lei, Yu Li, Xiaoliang Wang, Yi Liu, Gaohua Yang, Yanhui Luo, Lei Li, Ji J Cardiothorac Surg Case Report BACKGROUND: Azygos vein aneurysms (AVAs) are extremely rare. The majority of patients have no obvious clinical symptoms, so they are found by physical examination or by chance. There is limited clinical treatment experience that can be referred to, and there are no clear guidelines or research evidence standardizing the surgical and interventional therapy. Here, we report a patient with idiopathic AVA whose three-dimensional reconstruction of the tumor was completed before surgery. On the basis of three-dimensional reconstruction, single-port thoracoscopic resection of the AVA was successfully completed and reported for the first time. The previously reported cases are summarized to provide guidance for the diagnosis and treatment of patients with AVAs. CASE PRESENTATION: A 56-year-old man was transferred to our hospital due to “dysphagia”. The diagnosis of AVA was made after enhanced computed tomography, gastroscopy, fiberoptic bronchoscopy, and three-dimensional reconstruction. Congenital weakness or degenerative changes causes the vein walls to be extremely thin that the AVA had the risk of ruptur. Furthermore, the patient had symptoms of dysphagia, he received single-port thoracoscopic surgery. After the operation, his dysphagia disappeared. The postoperative pathology confirmed hemangioma. The patient was discharged 3 days after surgery without any complications. CONCLUSIONS: AVAs are rare. Preoperative three-dimensional reconstruction can greatly help surgeons clarify the disease diagnosis, formulate the surgical plan, avoid damage to the surrounding vital organs, and reduce intraoperative bleeding. Thoracoscopic surgery to remove AVAs is difficult and has a high risk of bleeding, while more minimally invasive single-port thoracoscopic surgery is also safe and effective for the treatment of AVAs. BioMed Central 2023-01-16 /pmc/articles/PMC9844024/ /pubmed/36647165 http://dx.doi.org/10.1186/s13019-023-02143-2 Text en © The Author(s) 2023 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, Yi Hu, Qiuxia Xie, Xiaoyang Liu, Caiyang Lei, Yu Li, Xiaoliang Wang, Yi Liu, Gaohua Yang, Yanhui Luo, Lei Li, Ji Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title | Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title_full | Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title_fullStr | Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title_full_unstemmed | Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title_short | Single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
title_sort | single-port thoracoscopic removal of an azygos vein aneurysm: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844024/ https://www.ncbi.nlm.nih.gov/pubmed/36647165 http://dx.doi.org/10.1186/s13019-023-02143-2 |
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