Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report

Abstract Introduction Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complications. We herein describe an individualized treat...

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Main Authors: Jiayu Shen, Changping Gan, R. D. T. Rajaguru, Dou Yuan, Zhenghua Xiao
Format: Article
Language:English
Published: BMC 2020-09-01
Series:Journal of Cardiothoracic Surgery
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13019-020-01304-x
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spelling doaj-9eb97cdbd0ee405e848001cbe846bc722020-11-25T03:42:33ZengBMCJournal of Cardiothoracic Surgery1749-80902020-09-011511510.1186/s13019-020-01304-xManagement of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case reportJiayu Shen0Changping Gan1R. D. T. Rajaguru2Dou Yuan3Zhenghua Xiao4Department of Cardiovascular Surgery, West China Hospital of Sichuan UniversityDepartment of Cardiovascular Surgery, West China Hospital of Sichuan UniversityDepartment of Cardiovascular Surgery, West China Hospital of Sichuan UniversityDepartment of Cardiovascular Surgery, West China Hospital of Sichuan UniversityDepartment of Cardiovascular Surgery, West China Hospital of Sichuan UniversityAbstract Introduction Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complications. We herein describe an individualized treatment decision-making process for a 23-year-old male with MFS, suffering from a giant but stable aortic root aneurysm which is extremely rare at his age. Case The patient, a 23-year-old male with a family history of MFS, presented to our cardiovascular department because of progressive exertional chest distress, fatigue and occasional precordial pain. Physical examinations revealed 190.5 cm of height, high myopia, and a diastolic murmur at the aortic valve area. Laboratory examinations for systemic vasculitis and infectious diseases were negative. Transthoracic echocardiography and enhanced thoracic computed tomography (CT) scan revealed the existence of a giant aortic root aneurysm (125.1 mm in short-axis), severe aortic valve regurgitation, cardiac dilatation (LV; 99 mm in diastolic diameter) and a poor ejection fraction (EF; 18%). Considering the risk of rupture or dissection of the dilated aortic root, we performed Bentall procedure based on the results of multidisciplinary team discussion and intraoperative exploration. Postoperative thoracic CT scan revealed a normal sized reconstructed aortic root, and the patient was discharged uneventfully 7 days later. Conclusion It is extremely rare to report such a giant aortic root aneurysm in a young patient. In the treatment decision-making process, the patient’s specific situation should be taken into consideration. A mechanical Bentall procedure seems to be an acceptable option for some selected cases.http://link.springer.com/article/10.1186/s13019-020-01304-xAortic aneurysmCardiac surgeryDilated aortic rootMarfan syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Jiayu Shen
Changping Gan
R. D. T. Rajaguru
Dou Yuan
Zhenghua Xiao
spellingShingle Jiayu Shen
Changping Gan
R. D. T. Rajaguru
Dou Yuan
Zhenghua Xiao
Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
Journal of Cardiothoracic Surgery
Aortic aneurysm
Cardiac surgery
Dilated aortic root
Marfan syndrome
author_facet Jiayu Shen
Changping Gan
R. D. T. Rajaguru
Dou Yuan
Zhenghua Xiao
author_sort Jiayu Shen
title Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
title_short Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
title_full Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
title_fullStr Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
title_full_unstemmed Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
title_sort management of a giant aortic root aneurysm in a young patient with marfan syndrome: a case report
publisher BMC
series Journal of Cardiothoracic Surgery
issn 1749-8090
publishDate 2020-09-01
description Abstract Introduction Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complications. We herein describe an individualized treatment decision-making process for a 23-year-old male with MFS, suffering from a giant but stable aortic root aneurysm which is extremely rare at his age. Case The patient, a 23-year-old male with a family history of MFS, presented to our cardiovascular department because of progressive exertional chest distress, fatigue and occasional precordial pain. Physical examinations revealed 190.5 cm of height, high myopia, and a diastolic murmur at the aortic valve area. Laboratory examinations for systemic vasculitis and infectious diseases were negative. Transthoracic echocardiography and enhanced thoracic computed tomography (CT) scan revealed the existence of a giant aortic root aneurysm (125.1 mm in short-axis), severe aortic valve regurgitation, cardiac dilatation (LV; 99 mm in diastolic diameter) and a poor ejection fraction (EF; 18%). Considering the risk of rupture or dissection of the dilated aortic root, we performed Bentall procedure based on the results of multidisciplinary team discussion and intraoperative exploration. Postoperative thoracic CT scan revealed a normal sized reconstructed aortic root, and the patient was discharged uneventfully 7 days later. Conclusion It is extremely rare to report such a giant aortic root aneurysm in a young patient. In the treatment decision-making process, the patient’s specific situation should be taken into consideration. A mechanical Bentall procedure seems to be an acceptable option for some selected cases.
topic Aortic aneurysm
Cardiac surgery
Dilated aortic root
Marfan syndrome
url http://link.springer.com/article/10.1186/s13019-020-01304-x
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