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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,...

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Autores principales: Maffei, Rafael Tuzino Leite Neves, Fortuna, Giulio de los Santos, Rosso, Luca Campolino, Pires, Pedro Dragone, Rondelli, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2020
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.
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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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