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Arrhythmogenic Noncompaction Cardiomyopathy: Is There an Echocardiographic Phenotypic Overlap of Two Distinct Cardiomyopathies?

The clinical diagnosis of right ventricular (RV) cardiomyopathies is often challenging. It is difficult to differentiate the isolated left ventricular (LV) noncompaction cardiomyopathy (NC) from biventricular NC or from coexisting arrhythmogenic ventricular cardiomyopathy (AC). There are currently f...

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Detalles Bibliográficos
Autores principales: Aras, Dursun, Ozeke, Ozcan, Cay, Serkan, Ozcan, Firat, Baser, Kazım, Dogan, Umuttan, Unlu, Murat, Demirkan, Burcu, Tufekcioglu, Omac, Topaloglu, Serkan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Echocardiography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595707/
https://www.ncbi.nlm.nih.gov/pubmed/26448828
http://dx.doi.org/10.4250/jcu.2015.23.3.186
Descripción
Sumario:The clinical diagnosis of right ventricular (RV) cardiomyopathies is often challenging. It is difficult to differentiate the isolated left ventricular (LV) noncompaction cardiomyopathy (NC) from biventricular NC or from coexisting arrhythmogenic ventricular cardiomyopathy (AC). There are currently few established morphologic criteria for the diagnosis other than RV dilation and presence of excessive regional trabeculation. The gross and microscopic changes suggest pathological similarities between, or coexistence of, RV-NC and AC. Therefore, the term arrhythmogenic right ventricular cardiomyopathy is somewhat misleading as isolated LV or biventricular involvement may be present and thus a broader term such as AC should be preferred. We describe an unusual case of AC associated with a NC in a 27-year-old man who had a history of permanent pacemaker 7 years ago due to second-degree atrioventricular block.