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Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report
BACKGROUND: Marfan syndrome (MFS) is a connective tissue disorder involving multiple organs. The most severe complications include aortic root dilatation and dissection. In the present report, we provide an uncommon case of acute aortic Stanford type A dissection (AADA) repair with severe scoliosis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652535/ https://www.ncbi.nlm.nih.gov/pubmed/36388824 http://dx.doi.org/10.21037/atm-22-4302 |
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author | Huang, Shengbo Yang, Xiaorong Liu, Daxing Tang, Quan Guo, Ke Zhang, Jian |
author_facet | Huang, Shengbo Yang, Xiaorong Liu, Daxing Tang, Quan Guo, Ke Zhang, Jian |
author_sort | Huang, Shengbo |
collection | PubMed |
description | BACKGROUND: Marfan syndrome (MFS) is a connective tissue disorder involving multiple organs. The most severe complications include aortic root dilatation and dissection. In the present report, we provide an uncommon case of acute aortic Stanford type A dissection (AADA) repair with severe scoliosis in an MFS patient and it is even more rare for such surgical treatment to be successfully completed along with holistic management that enables the patient to recover successfully. We offer a reference for future surgical therapy since the specific surgical treatment methods in this case have not been reported in the literature. CASE DESCRIPTION: A 40-year-old Chinese female with MFS was rushed to our surgical clinic due to the sudden onset of intense chest pain. Physical examination revealed a diastolic murmur at the aortic valve area, increased arm and pectus carinatum deformity, severe scoliosis, acromicria, arachnodactyly, and planovalgus foot. Subsequently, AADA was discovered through computed tomography scan. In addition, echocardiogram revealed moderate aortic regurgitation and hydropericardium in small amount. Based on revised Ghent criteria, the patient was diagnosed with MFS complicated with aortic dissection. Emergency surgery was successfully performed for repair of the patient’s aortic dissection and the diseased aortic valve. Postoperatively, the patient presented with a degree of respiratory insufficiency. However, the respiratory function was not greatly impaired, with good early intervention, such as taking deep breaths and coughing fully, active sputum suction, effective analgesia, ambulation and treadmill exercise. The patient finally recovered completely and was discharged 3 weeks later. CONCLUSIONS: We reported on a patient with severe scoliosis who successfully underwent surgical repair of AADA. Our report shows that the application of standard median sternotomy for repairing AADA offers the feasibility of implementation, on the basis of effectively solving various practical problems in the surgery brought about by scoliosis. It has been thoroughly assessed and addressed how the postoperative condition of such patients affects subsequent respiratory function and postoperative recovery. This report further provides a successful clinical reference for the implementation of this type of surgery and the postoperative management of respiratory function. |
format | Online Article Text |
id | pubmed-9652535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-96525352022-11-15 Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report Huang, Shengbo Yang, Xiaorong Liu, Daxing Tang, Quan Guo, Ke Zhang, Jian Ann Transl Med Case Report BACKGROUND: Marfan syndrome (MFS) is a connective tissue disorder involving multiple organs. The most severe complications include aortic root dilatation and dissection. In the present report, we provide an uncommon case of acute aortic Stanford type A dissection (AADA) repair with severe scoliosis in an MFS patient and it is even more rare for such surgical treatment to be successfully completed along with holistic management that enables the patient to recover successfully. We offer a reference for future surgical therapy since the specific surgical treatment methods in this case have not been reported in the literature. CASE DESCRIPTION: A 40-year-old Chinese female with MFS was rushed to our surgical clinic due to the sudden onset of intense chest pain. Physical examination revealed a diastolic murmur at the aortic valve area, increased arm and pectus carinatum deformity, severe scoliosis, acromicria, arachnodactyly, and planovalgus foot. Subsequently, AADA was discovered through computed tomography scan. In addition, echocardiogram revealed moderate aortic regurgitation and hydropericardium in small amount. Based on revised Ghent criteria, the patient was diagnosed with MFS complicated with aortic dissection. Emergency surgery was successfully performed for repair of the patient’s aortic dissection and the diseased aortic valve. Postoperatively, the patient presented with a degree of respiratory insufficiency. However, the respiratory function was not greatly impaired, with good early intervention, such as taking deep breaths and coughing fully, active sputum suction, effective analgesia, ambulation and treadmill exercise. The patient finally recovered completely and was discharged 3 weeks later. CONCLUSIONS: We reported on a patient with severe scoliosis who successfully underwent surgical repair of AADA. Our report shows that the application of standard median sternotomy for repairing AADA offers the feasibility of implementation, on the basis of effectively solving various practical problems in the surgery brought about by scoliosis. It has been thoroughly assessed and addressed how the postoperative condition of such patients affects subsequent respiratory function and postoperative recovery. This report further provides a successful clinical reference for the implementation of this type of surgery and the postoperative management of respiratory function. AME Publishing Company 2022-10 /pmc/articles/PMC9652535/ /pubmed/36388824 http://dx.doi.org/10.21037/atm-22-4302 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Huang, Shengbo Yang, Xiaorong Liu, Daxing Tang, Quan Guo, Ke Zhang, Jian Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title | Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title_full | Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title_fullStr | Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title_full_unstemmed | Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title_short | Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report |
title_sort | successful management of stanford type a aortic dissection with severe scoliosis in the setting of marfan syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652535/ https://www.ncbi.nlm.nih.gov/pubmed/36388824 http://dx.doi.org/10.21037/atm-22-4302 |
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