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Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report

The association of Standford type A acute aortic dissection with situs inversus totalis (SIT) is extremely rare and only a few cases are reported in the literature to date. Due to the particular rarity, this unusual condition, if not diagnosed quickly and correctly, can generate both clinical and su...

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Autores principales: De Masi De Luca, Gabriele, Nicolardi, Salvatore, Mangia, Federica, Zaccaria, Salvatore, Palamà, Zefferino, Tridici, Maurizio, Papadia, Paola, De Masi De Luca, Giuseppe, Accogli, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205311/
https://www.ncbi.nlm.nih.gov/pubmed/37228910
http://dx.doi.org/10.1097/MS9.0000000000000647
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author De Masi De Luca, Gabriele
Nicolardi, Salvatore
Mangia, Federica
Zaccaria, Salvatore
Palamà, Zefferino
Tridici, Maurizio
Papadia, Paola
De Masi De Luca, Giuseppe
Accogli, Michele
author_facet De Masi De Luca, Gabriele
Nicolardi, Salvatore
Mangia, Federica
Zaccaria, Salvatore
Palamà, Zefferino
Tridici, Maurizio
Papadia, Paola
De Masi De Luca, Giuseppe
Accogli, Michele
author_sort De Masi De Luca, Gabriele
collection PubMed
description The association of Standford type A acute aortic dissection with situs inversus totalis (SIT) is extremely rare and only a few cases are reported in the literature to date. Due to the particular rarity, this unusual condition, if not diagnosed quickly and correctly, can generate both clinical and surgical difficulties. CASE PRESENTATION: We describe the case of a male Caucasian patient with SIT and aortic dissection type A, who occurred to our Emergency Department with a severe clinical condition of shock. Using the fast diagnostic approach with chest X-Ray and echocardiography followed by computed tomography investigation, a Standford type A acute aortic dissection and the presence of SIT were detected. The patient was subjected to surgical treatment with optimal results in a short time. CLINICAL DISCUSSION AND CONCLUSION: The event of aortic dissection is an extremely serious condition and the simultaneous presence of a critical clinical presentation with an unusual congenital anomaly could condition a correct and rapid diagnostic process. Only an accurate diagnostic investigation can give a quick diagnosis and useful elements for a correct therapeutic approach.
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spelling pubmed-102053112023-05-24 Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report De Masi De Luca, Gabriele Nicolardi, Salvatore Mangia, Federica Zaccaria, Salvatore Palamà, Zefferino Tridici, Maurizio Papadia, Paola De Masi De Luca, Giuseppe Accogli, Michele Ann Med Surg (Lond) Case Reports The association of Standford type A acute aortic dissection with situs inversus totalis (SIT) is extremely rare and only a few cases are reported in the literature to date. Due to the particular rarity, this unusual condition, if not diagnosed quickly and correctly, can generate both clinical and surgical difficulties. CASE PRESENTATION: We describe the case of a male Caucasian patient with SIT and aortic dissection type A, who occurred to our Emergency Department with a severe clinical condition of shock. Using the fast diagnostic approach with chest X-Ray and echocardiography followed by computed tomography investigation, a Standford type A acute aortic dissection and the presence of SIT were detected. The patient was subjected to surgical treatment with optimal results in a short time. CLINICAL DISCUSSION AND CONCLUSION: The event of aortic dissection is an extremely serious condition and the simultaneous presence of a critical clinical presentation with an unusual congenital anomaly could condition a correct and rapid diagnostic process. Only an accurate diagnostic investigation can give a quick diagnosis and useful elements for a correct therapeutic approach. Lippincott Williams & Wilkins 2023-04-18 /pmc/articles/PMC10205311/ /pubmed/37228910 http://dx.doi.org/10.1097/MS9.0000000000000647 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/) License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Case Reports
De Masi De Luca, Gabriele
Nicolardi, Salvatore
Mangia, Federica
Zaccaria, Salvatore
Palamà, Zefferino
Tridici, Maurizio
Papadia, Paola
De Masi De Luca, Giuseppe
Accogli, Michele
Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title_full Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title_fullStr Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title_full_unstemmed Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title_short Standford type A aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
title_sort standford type a aortic dissection in a patient with situs inversus totalis, with critical clinical presentation: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205311/
https://www.ncbi.nlm.nih.gov/pubmed/37228910
http://dx.doi.org/10.1097/MS9.0000000000000647
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