Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up

We present a 15-year follow-up after aorto-aortic bypass surgery in a 7-month-old infant with middle aortic syndrome and confirmed Marfan syndrome. In anticipation of her growth, the length of the graft was adjusted to the anticipated length of the narrowed aorta in her adolescence. In addition, her...

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Autores principales: Heck, Roland, Fischer-Zirnsak, Björn, Photiadis, Joachim, Horn, Denise, Gehle, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Congenital Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931065/
https://www.ncbi.nlm.nih.gov/pubmed/36802262
http://dx.doi.org/10.1093/icvts/ivad011
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author Heck, Roland
Fischer-Zirnsak, Björn
Photiadis, Joachim
Horn, Denise
Gehle, Petra
author_facet Heck, Roland
Fischer-Zirnsak, Björn
Photiadis, Joachim
Horn, Denise
Gehle, Petra
author_sort Heck, Roland
collection PubMed
description We present a 15-year follow-up after aorto-aortic bypass surgery in a 7-month-old infant with middle aortic syndrome and confirmed Marfan syndrome. In anticipation of her growth, the length of the graft was adjusted to the anticipated length of the narrowed aorta in her adolescence. In addition, her height was controlled by oestrogen, and her growth was stopped at 178 cm. To date, the patient is free from aortic reoperation and lower limb malperfusion.
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spelling pubmed-99310652023-02-16 Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up Heck, Roland Fischer-Zirnsak, Björn Photiadis, Joachim Horn, Denise Gehle, Petra Interdiscip Cardiovasc Thorac Surg Congenital Disease We present a 15-year follow-up after aorto-aortic bypass surgery in a 7-month-old infant with middle aortic syndrome and confirmed Marfan syndrome. In anticipation of her growth, the length of the graft was adjusted to the anticipated length of the narrowed aorta in her adolescence. In addition, her height was controlled by oestrogen, and her growth was stopped at 178 cm. To date, the patient is free from aortic reoperation and lower limb malperfusion. Oxford University Press 2023-01-19 /pmc/articles/PMC9931065/ /pubmed/36802262 http://dx.doi.org/10.1093/icvts/ivad011 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Congenital Disease
Heck, Roland
Fischer-Zirnsak, Björn
Photiadis, Joachim
Horn, Denise
Gehle, Petra
Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title_full Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title_fullStr Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title_full_unstemmed Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title_short Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
title_sort aorto-aortic bypass in an infant with middle aortic syndrome and marfan syndrome: a 15-year follow-up
topic Congenital Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931065/
https://www.ncbi.nlm.nih.gov/pubmed/36802262
http://dx.doi.org/10.1093/icvts/ivad011
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