Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?

Arrhythmogenic cardiomyopathy is a biventricular disease in which the effect on the left ventricle can be either equivalent to or more severe than that on the right ventricle. It is a rare disease due to its low reported prevalence and typically becomes clinically evident during the second to fourth...

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Main Authors: Santiago Luna-Alcala, MD, Mauricio Garcia-Cardenas, MD, Enrique C. Guerra, MD, Pavel Martinez-Dominguez, MD, Aldo Cabello-Ganem, MD, Leonardo Proaño-Bernal, MD, Cristian A. Chava-Ponte, MD, Arturo Hernandez-Pacherres, MD, Nilda Espinola-Zavaleta, MD, PhD
Format: Article
Language:English
Published: Elsevier 2024-06-01
Series:Radiology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043324002206
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author Santiago Luna-Alcala, MD
Mauricio Garcia-Cardenas, MD
Enrique C. Guerra, MD
Pavel Martinez-Dominguez, MD
Aldo Cabello-Ganem, MD
Leonardo Proaño-Bernal, MD
Cristian A. Chava-Ponte, MD
Arturo Hernandez-Pacherres, MD
Nilda Espinola-Zavaleta, MD, PhD
author_facet Santiago Luna-Alcala, MD
Mauricio Garcia-Cardenas, MD
Enrique C. Guerra, MD
Pavel Martinez-Dominguez, MD
Aldo Cabello-Ganem, MD
Leonardo Proaño-Bernal, MD
Cristian A. Chava-Ponte, MD
Arturo Hernandez-Pacherres, MD
Nilda Espinola-Zavaleta, MD, PhD
author_sort Santiago Luna-Alcala, MD
collection DOAJ
description Arrhythmogenic cardiomyopathy is a biventricular disease in which the effect on the left ventricle can be either equivalent to or more severe than that on the right ventricle. It is a rare disease due to its low reported prevalence and typically becomes clinically evident during the second to fourth decade of life. It represents 4% of sudden cardiac death cases referred for autopsy and 10% of cases of unexplained cardiac arrest. We present a challenging case report of a 68-year-old man who arrived at the emergency room with chest discomfort, palpitations, and light-headedness before a syncopal episode with urinary incontinence. During monitoring, ventricular tachycardia was detected and was treated with cardioversion. However, a follow-up electrocardiogram revealed low QRS voltages in limb leads and T-wave inversion in the left precordial leads. The patient underwent a transthoracic echocardiogram and a gadolinium-based magnetic resonance imaging study to evaluate the possibility of acute decompensated heart failure. Both imaging studies revealed low ejection fraction and systolic dysfunction in both right and left ventricles. Furthermore, in the late gadolinium enhancement study, extensive left ventricular subepicardial enhancement with septal predominance in a ring pattern and an irregular morphology of the right ventricular free wall were observed. A diagnosis of biventricular arrhythmogenic cardiomyopathy was established based on the 2020 Padua Criteria. Although there is not a recognized classification within these criteria to establish its subtype, in our case there was a left ventricular predominance due to the presence of additional left ventricular categories.
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spelling doaj.art-3fac2276e4304982b56399d4a2b852e52024-03-30T04:39:01ZengElsevierRadiology Case Reports1930-04332024-06-0119624572463Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?Santiago Luna-Alcala, MD0Mauricio Garcia-Cardenas, MD1Enrique C. Guerra, MD2Pavel Martinez-Dominguez, MD3Aldo Cabello-Ganem, MD4Leonardo Proaño-Bernal, MD5Cristian A. Chava-Ponte, MD6Arturo Hernandez-Pacherres, MD7Nilda Espinola-Zavaleta, MD, PhD8Department of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, MexicoDepartment of Magnetic Resonance, San Pablo Clinic, Lima, PeruDepartment of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, Mexico; MD–PhD (PECEM) Program, School of Medicine, National Autonomous University of Mexico, Mexico City, MexicoDepartment of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, MexicoDepartment of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, MexicoDepartment of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, MexicoDepartment of Cardiology, Hipolito Unanue National Hospital, Lima, PeruDepartment of Cardiology, Hipolito Unanue National Hospital, Lima, PeruDepartment of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Mexico City, Mexico; Corresponding author.Arrhythmogenic cardiomyopathy is a biventricular disease in which the effect on the left ventricle can be either equivalent to or more severe than that on the right ventricle. It is a rare disease due to its low reported prevalence and typically becomes clinically evident during the second to fourth decade of life. It represents 4% of sudden cardiac death cases referred for autopsy and 10% of cases of unexplained cardiac arrest. We present a challenging case report of a 68-year-old man who arrived at the emergency room with chest discomfort, palpitations, and light-headedness before a syncopal episode with urinary incontinence. During monitoring, ventricular tachycardia was detected and was treated with cardioversion. However, a follow-up electrocardiogram revealed low QRS voltages in limb leads and T-wave inversion in the left precordial leads. The patient underwent a transthoracic echocardiogram and a gadolinium-based magnetic resonance imaging study to evaluate the possibility of acute decompensated heart failure. Both imaging studies revealed low ejection fraction and systolic dysfunction in both right and left ventricles. Furthermore, in the late gadolinium enhancement study, extensive left ventricular subepicardial enhancement with septal predominance in a ring pattern and an irregular morphology of the right ventricular free wall were observed. A diagnosis of biventricular arrhythmogenic cardiomyopathy was established based on the 2020 Padua Criteria. Although there is not a recognized classification within these criteria to establish its subtype, in our case there was a left ventricular predominance due to the presence of additional left ventricular categories.http://www.sciencedirect.com/science/article/pii/S1930043324002206Biventricular cardiomyopathyLeft ventricleFibrosisImplantable cardioverter defibrillatorSudden cardiac deathVentricular tachycardia
spellingShingle Santiago Luna-Alcala, MD
Mauricio Garcia-Cardenas, MD
Enrique C. Guerra, MD
Pavel Martinez-Dominguez, MD
Aldo Cabello-Ganem, MD
Leonardo Proaño-Bernal, MD
Cristian A. Chava-Ponte, MD
Arturo Hernandez-Pacherres, MD
Nilda Espinola-Zavaleta, MD, PhD
Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
Radiology Case Reports
Biventricular cardiomyopathy
Left ventricle
Fibrosis
Implantable cardioverter defibrillator
Sudden cardiac death
Ventricular tachycardia
title Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
title_full Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
title_fullStr Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
title_full_unstemmed Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
title_short Ventricular predominance in biventricular arrhythmogenic cardiomyopathy: Should new subtype criteria be recognized?
title_sort ventricular predominance in biventricular arrhythmogenic cardiomyopathy should new subtype criteria be recognized
topic Biventricular cardiomyopathy
Left ventricle
Fibrosis
Implantable cardioverter defibrillator
Sudden cardiac death
Ventricular tachycardia
url http://www.sciencedirect.com/science/article/pii/S1930043324002206
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