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Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report

BACKGROUND: Intercostal artery pseudoaneurysm is rare and at the risk of rupture. The aetiology is always reported to be iatrogenic and traumatic injury. Embolisation is the most common therapeutic method. Here, we report a case of spontaneous intercostal artery pseudoaneurysm and cured by combining...

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Autores principales: Liu, Caiyang, Ran, Ran, Li, Xiaoliang, Liu, Gaohua, Wang, Chuanxi, Li, Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166138/
https://www.ncbi.nlm.nih.gov/pubmed/34059107
http://dx.doi.org/10.1186/s13019-021-01548-1
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author Liu, Caiyang
Ran, Ran
Li, Xiaoliang
Liu, Gaohua
Wang, Chuanxi
Li, Ji
author_facet Liu, Caiyang
Ran, Ran
Li, Xiaoliang
Liu, Gaohua
Wang, Chuanxi
Li, Ji
author_sort Liu, Caiyang
collection PubMed
description BACKGROUND: Intercostal artery pseudoaneurysm is rare and at the risk of rupture. The aetiology is always reported to be iatrogenic and traumatic injury. Embolisation is the most common therapeutic method. Here, we report a case of spontaneous intercostal artery pseudoaneurysm and cured by combining covered stent grafting and surgical management. CASE PRESENTATION: A 60-year-old man complained of acute right back pain for 5 h. Computed tomography showed right massive hemothorax and a giant mass with distinct feeding vessel originated from the thoracic aorta within the right hemithorax. Thoracocentesis was performed, and then a covered stent was positioned across the origin of the feeding vessel. The patient was diagnosed with intercostal artery pseudoaneurysm. Finally, we successfully resected the pseudoaneurysm and ligated the proximal part of the artery. Histologic examination have proved the diagnosis. The postoperative course was uneventful, and the patient was discharged on postoperative day 10. There is no recurrence reported during follow-up. CONCLUSIONS: Spontaneous intercostal artery pseudoaneurysm is extremly rare. Delayed hemothorax due to rupture of the pseudoaneurysm may occur years after the formation. Early diagnosis is important and a combined treatment of endovascular intervention and surgical management is feasible, especially for the case of ruptured large tumour-like mass presentation of the pseudoaneurysm.
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spelling pubmed-81661382021-06-02 Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report Liu, Caiyang Ran, Ran Li, Xiaoliang Liu, Gaohua Wang, Chuanxi Li, Ji J Cardiothorac Surg Case Report BACKGROUND: Intercostal artery pseudoaneurysm is rare and at the risk of rupture. The aetiology is always reported to be iatrogenic and traumatic injury. Embolisation is the most common therapeutic method. Here, we report a case of spontaneous intercostal artery pseudoaneurysm and cured by combining covered stent grafting and surgical management. CASE PRESENTATION: A 60-year-old man complained of acute right back pain for 5 h. Computed tomography showed right massive hemothorax and a giant mass with distinct feeding vessel originated from the thoracic aorta within the right hemithorax. Thoracocentesis was performed, and then a covered stent was positioned across the origin of the feeding vessel. The patient was diagnosed with intercostal artery pseudoaneurysm. Finally, we successfully resected the pseudoaneurysm and ligated the proximal part of the artery. Histologic examination have proved the diagnosis. The postoperative course was uneventful, and the patient was discharged on postoperative day 10. There is no recurrence reported during follow-up. CONCLUSIONS: Spontaneous intercostal artery pseudoaneurysm is extremly rare. Delayed hemothorax due to rupture of the pseudoaneurysm may occur years after the formation. Early diagnosis is important and a combined treatment of endovascular intervention and surgical management is feasible, especially for the case of ruptured large tumour-like mass presentation of the pseudoaneurysm. BioMed Central 2021-05-31 /pmc/articles/PMC8166138/ /pubmed/34059107 http://dx.doi.org/10.1186/s13019-021-01548-1 Text en © The Author(s) 2021 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
Liu, Caiyang
Ran, Ran
Li, Xiaoliang
Liu, Gaohua
Wang, Chuanxi
Li, Ji
Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title_full Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title_fullStr Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title_full_unstemmed Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title_short Massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
title_sort massive hemothorax caused by intercostal artery pseudoaneurysm:a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166138/
https://www.ncbi.nlm.nih.gov/pubmed/34059107
http://dx.doi.org/10.1186/s13019-021-01548-1
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