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Cardiomyopathy as the first manifestation of Friedreich's ataxia
We present the case of a female patient diagnosed in childhood with Friedreich Ataxia (FA). At the age of 6, she developed left congestive heart failure with cardiomyopathy, as evident on echocardiogram. Neurologic signs only appeared at age 7, including marked loss of muscle mass, gait instability,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
São Paulo, SP: Universidade de São Paulo, Hospital Universitário
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703435/ https://www.ncbi.nlm.nih.gov/pubmed/33344308 http://dx.doi.org/10.4322/acr.2020.204 |
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author | Maffei, Rafael Tuzino Leite Neves Fortuna, Giulio de los Santos Rosso, Luca Campolino Pires, Pedro Dragone Rondelli, Ivan |
author_facet | Maffei, Rafael Tuzino Leite Neves Fortuna, Giulio de los Santos Rosso, Luca Campolino Pires, Pedro Dragone Rondelli, Ivan |
author_sort | Maffei, Rafael Tuzino Leite Neves |
collection | PubMed |
description | We present the case of a female patient diagnosed in childhood with Friedreich Ataxia (FA). At the age of 6, she developed left congestive heart failure with cardiomyopathy, as evident on echocardiogram. Neurologic signs only appeared at age 7, including marked loss of muscle mass, gait instability, muscle clonus, and Babinski's signal. At age 27, she had a stroke and was hospitalized; a few days later, she had a cardiorespiratory arrest with asystole, leading to death. The autopsy disclosed severe cardiomyopathy and significant myocardial replacement with fibrosis; therefore, the cause of death was assumed to be heart failure. Compared to the literature, our case has some unique features, such as cardiac disease as the presenting manifestation instead of gait instability, which is the major initial sign in most FA cases. Since our patient was submitted to an autopsy, it was an opportunity to retrieve important data to confirm the diagnosis and to evaluate the pathophysiology of this entity, such as myocardium fibrosis and cerebellar degeneration. In summary, our case demonstrates that cardiac disease can be the first manifestation of FA, with eventual diagnostic and prognostic implications. In addition, the autopsy provided findings of severe cardiomyopathy associated with FA. |
format | Online Article Text |
id | pubmed-7703435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | São Paulo, SP: Universidade de São Paulo, Hospital Universitário |
record_format | MEDLINE/PubMed |
spelling | pubmed-77034352020-12-18 Cardiomyopathy as the first manifestation of Friedreich's ataxia Maffei, Rafael Tuzino Leite Neves Fortuna, Giulio de los Santos Rosso, Luca Campolino Pires, Pedro Dragone Rondelli, Ivan Autops Case Rep Autopsy Case Report We present the case of a female patient diagnosed in childhood with Friedreich Ataxia (FA). At the age of 6, she developed left congestive heart failure with cardiomyopathy, as evident on echocardiogram. Neurologic signs only appeared at age 7, including marked loss of muscle mass, gait instability, muscle clonus, and Babinski's signal. At age 27, she had a stroke and was hospitalized; a few days later, she had a cardiorespiratory arrest with asystole, leading to death. The autopsy disclosed severe cardiomyopathy and significant myocardial replacement with fibrosis; therefore, the cause of death was assumed to be heart failure. Compared to the literature, our case has some unique features, such as cardiac disease as the presenting manifestation instead of gait instability, which is the major initial sign in most FA cases. Since our patient was submitted to an autopsy, it was an opportunity to retrieve important data to confirm the diagnosis and to evaluate the pathophysiology of this entity, such as myocardium fibrosis and cerebellar degeneration. In summary, our case demonstrates that cardiac disease can be the first manifestation of FA, with eventual diagnostic and prognostic implications. In addition, the autopsy provided findings of severe cardiomyopathy associated with FA. São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2020-09-10 /pmc/articles/PMC7703435/ /pubmed/33344308 http://dx.doi.org/10.4322/acr.2020.204 Text en Copyright: © 2020 The Authors. https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Autopsy Case Report Maffei, Rafael Tuzino Leite Neves Fortuna, Giulio de los Santos Rosso, Luca Campolino Pires, Pedro Dragone Rondelli, Ivan Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title | Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title_full | Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title_fullStr | Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title_full_unstemmed | Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title_short | Cardiomyopathy as the first manifestation of Friedreich's ataxia |
title_sort | cardiomyopathy as the first manifestation of friedreich's ataxia |
topic | Autopsy Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703435/ https://www.ncbi.nlm.nih.gov/pubmed/33344308 http://dx.doi.org/10.4322/acr.2020.204 |
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