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Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature
BACKGROUND: Spindle cell sarcomas of the right atrium are extremely rare primary cardiac tumours, with very few cases reported in the medical literature. Pseudoaneurysms caused by cardiac spindle cell sarcoma have never been reported worldwide. CASE PRESENTATION: A 32-year-old woman was referred to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980566/ https://www.ncbi.nlm.nih.gov/pubmed/33741020 http://dx.doi.org/10.1186/s13019-021-01404-2 |
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author | Wang, Xiaofang Dong, Aiqiang Yang, Weijun Duan, Qunjun |
author_facet | Wang, Xiaofang Dong, Aiqiang Yang, Weijun Duan, Qunjun |
author_sort | Wang, Xiaofang |
collection | PubMed |
description | BACKGROUND: Spindle cell sarcomas of the right atrium are extremely rare primary cardiac tumours, with very few cases reported in the medical literature. Pseudoaneurysms caused by cardiac spindle cell sarcoma have never been reported worldwide. CASE PRESENTATION: A 32-year-old woman was referred to our hospital for recurrent pericardial haemorrhagic effusion and pleural effusion. Three-dimensional transthoracic echocardiogram, contrast chest CT, and contrast MRI revealed a pseudoaneurysm on the right side of the right atrium with a thrombus. There was a defect between the pseudoaneurysm and the right atrium. PET-CT suggested that FDG metabolism inhomogeneity increased in the mass in the right atrium. Exfoliative cytology detection of massive pericardial effusion and pleural effusion revealed no tumour cells. Spindle cell sarcoma of the right atrium was not confirmed until the patient underwent right thoracic exploration and biopsy. Before a confirmed diagnosis, symptomatic treatment, such as chest effusion and pericardium effusion drainage, and transfusion of red blood cells were mainly used to relieve the patient’s symptoms. Unfortunately, the patient was lost to optimal treatments and passed away 20 days after the pathological diagnosis was made. CONCLUSION: The prognosis of spindle cell sarcomas remains poor due to delays in diagnosis, early metastasis and few available therapeutic options. Recurrent pericardial effusion and pleural effusion, especially in the nature of haemorrhagic effusion, and/or right atrial pseudoaneurysm shown on the transthoracic echocardiogram must be considered and highly suspected as malignancy by patients and physicians. If the diagnosis cannot be confirmed, histopathology should be performed as soon as possible to avoid losing the best treatment opportunity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13019-021-01404-2. |
format | Online Article Text |
id | pubmed-7980566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79805662021-03-22 Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature Wang, Xiaofang Dong, Aiqiang Yang, Weijun Duan, Qunjun J Cardiothorac Surg Case Report BACKGROUND: Spindle cell sarcomas of the right atrium are extremely rare primary cardiac tumours, with very few cases reported in the medical literature. Pseudoaneurysms caused by cardiac spindle cell sarcoma have never been reported worldwide. CASE PRESENTATION: A 32-year-old woman was referred to our hospital for recurrent pericardial haemorrhagic effusion and pleural effusion. Three-dimensional transthoracic echocardiogram, contrast chest CT, and contrast MRI revealed a pseudoaneurysm on the right side of the right atrium with a thrombus. There was a defect between the pseudoaneurysm and the right atrium. PET-CT suggested that FDG metabolism inhomogeneity increased in the mass in the right atrium. Exfoliative cytology detection of massive pericardial effusion and pleural effusion revealed no tumour cells. Spindle cell sarcoma of the right atrium was not confirmed until the patient underwent right thoracic exploration and biopsy. Before a confirmed diagnosis, symptomatic treatment, such as chest effusion and pericardium effusion drainage, and transfusion of red blood cells were mainly used to relieve the patient’s symptoms. Unfortunately, the patient was lost to optimal treatments and passed away 20 days after the pathological diagnosis was made. CONCLUSION: The prognosis of spindle cell sarcomas remains poor due to delays in diagnosis, early metastasis and few available therapeutic options. Recurrent pericardial effusion and pleural effusion, especially in the nature of haemorrhagic effusion, and/or right atrial pseudoaneurysm shown on the transthoracic echocardiogram must be considered and highly suspected as malignancy by patients and physicians. If the diagnosis cannot be confirmed, histopathology should be performed as soon as possible to avoid losing the best treatment opportunity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13019-021-01404-2. BioMed Central 2021-03-19 /pmc/articles/PMC7980566/ /pubmed/33741020 http://dx.doi.org/10.1186/s13019-021-01404-2 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Wang, Xiaofang Dong, Aiqiang Yang, Weijun Duan, Qunjun Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title | Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title_full | Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title_fullStr | Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title_full_unstemmed | Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title_short | Spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
title_sort | spindle cell sarcoma of the right atrium causing right atrial pseudoaneurysm: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980566/ https://www.ncbi.nlm.nih.gov/pubmed/33741020 http://dx.doi.org/10.1186/s13019-021-01404-2 |
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