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Aortic coarctation with cardiac fibroma in a young patient: a case report
BACKGROUND: Cardiac fibroma and aortic coarctation are rarely observed concomitantly in the same patient. We report a case of cardiac fibroma with aortic coarctation treated with a hybrid surgical procedure. To the best of our knowledge, this is the first case of these two abnormalities existing in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543761/ https://www.ncbi.nlm.nih.gov/pubmed/34708183 http://dx.doi.org/10.1093/ehjcr/ytab271 |
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author | Shen, Linghong Xu, Ke Kong, Ye He, Ben |
author_facet | Shen, Linghong Xu, Ke Kong, Ye He, Ben |
author_sort | Shen, Linghong |
collection | PubMed |
description | BACKGROUND: Cardiac fibroma and aortic coarctation are rarely observed concomitantly in the same patient. We report a case of cardiac fibroma with aortic coarctation treated with a hybrid surgical procedure. To the best of our knowledge, this is the first case of these two abnormalities existing in one patient. CASE SUMMARY: A 22-year-old female patient visited the clinic with a 10-year history of hypertension. Physical examination revealed blood pressure of the upper extremities 50 mmHg higher than that of the lower extremities. Computed tomography angiography revealed a post-ductal-type aortic coarctation at the beginning segment of the descending aorta along with a 7.7 cm × 5.1 cm left ventricular mass. Transthoracic echocardiogram showed a mass at the middle segments of the lateral wall and apex and posterior wall of the left ventricle. Cardiac magnetic resonance imaging also showed the mass with hypointense signal on T1, hyperintense signal on T2, and intense signal on late gadolinium enhancement. No evidences of metastatic lesions were observed on (18)F-fluorodeoxyglucose positron emission tomography. The patient underwent a hybrid surgery involving aortic stent implantation and complete left ventricular mass removal. The gradient between stenosis returned to <10 mmHg after the procedure. Pathologic findings revealed cardiac fibroma. DISCUSSION: It is rare to encounter a patient suffering from both cardiac fibroma and aortic coarctation. No evidences indicated a single cause or syndrome resulting in the coexistence of these two abnormalities. A hybrid surgery involving aortic stent implantation and complete cardiac mass resection could optimize the treatment in such cases. |
format | Online Article Text |
id | pubmed-8543761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85437612021-10-26 Aortic coarctation with cardiac fibroma in a young patient: a case report Shen, Linghong Xu, Ke Kong, Ye He, Ben Eur Heart J Case Rep Case Report BACKGROUND: Cardiac fibroma and aortic coarctation are rarely observed concomitantly in the same patient. We report a case of cardiac fibroma with aortic coarctation treated with a hybrid surgical procedure. To the best of our knowledge, this is the first case of these two abnormalities existing in one patient. CASE SUMMARY: A 22-year-old female patient visited the clinic with a 10-year history of hypertension. Physical examination revealed blood pressure of the upper extremities 50 mmHg higher than that of the lower extremities. Computed tomography angiography revealed a post-ductal-type aortic coarctation at the beginning segment of the descending aorta along with a 7.7 cm × 5.1 cm left ventricular mass. Transthoracic echocardiogram showed a mass at the middle segments of the lateral wall and apex and posterior wall of the left ventricle. Cardiac magnetic resonance imaging also showed the mass with hypointense signal on T1, hyperintense signal on T2, and intense signal on late gadolinium enhancement. No evidences of metastatic lesions were observed on (18)F-fluorodeoxyglucose positron emission tomography. The patient underwent a hybrid surgery involving aortic stent implantation and complete left ventricular mass removal. The gradient between stenosis returned to <10 mmHg after the procedure. Pathologic findings revealed cardiac fibroma. DISCUSSION: It is rare to encounter a patient suffering from both cardiac fibroma and aortic coarctation. No evidences indicated a single cause or syndrome resulting in the coexistence of these two abnormalities. A hybrid surgery involving aortic stent implantation and complete cardiac mass resection could optimize the treatment in such cases. Oxford University Press 2021-08-12 /pmc/articles/PMC8543761/ /pubmed/34708183 http://dx.doi.org/10.1093/ehjcr/ytab271 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Shen, Linghong Xu, Ke Kong, Ye He, Ben Aortic coarctation with cardiac fibroma in a young patient: a case report |
title | Aortic coarctation with cardiac fibroma in a young patient: a case report |
title_full | Aortic coarctation with cardiac fibroma in a young patient: a case report |
title_fullStr | Aortic coarctation with cardiac fibroma in a young patient: a case report |
title_full_unstemmed | Aortic coarctation with cardiac fibroma in a young patient: a case report |
title_short | Aortic coarctation with cardiac fibroma in a young patient: a case report |
title_sort | aortic coarctation with cardiac fibroma in a young patient: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543761/ https://www.ncbi.nlm.nih.gov/pubmed/34708183 http://dx.doi.org/10.1093/ehjcr/ytab271 |
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