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Sinus arrest in a p.Arg160X-DSP-positive patient without evidence of desmoplakin-mediated cardiomyopathy: a case report.
Tan, Nicholas Y; Giudicessi, John R; Harvey, Jason R; Asirvatham, Samuel J; Siontis, Konstantinos C.
Afiliação
  • Tan NY; Department of Cardiovascular Medicine, Mayo Clinic Rochester, Rochester, MN, United States.
  • Giudicessi JR; Department of Cardiovascular Medicine, Mayo Clinic Rochester, Rochester, MN, United States.
  • Harvey JR; Department of Cardiovascular Medicine, Mayo Clinic Rochester, Rochester, MN, United States.
  • Asirvatham SJ; Department of Cardiovascular Medicine, Mayo Clinic Rochester, Rochester, MN, United States.
  • Siontis KC; Department of Cardiovascular Medicine, Mayo Clinic Rochester, Rochester, MN, United States.
Front Cardiovasc Med ; 10: 1328898, 2023.
Article em En | MEDLINE | ID: mdl-38169814
ABSTRACT

Background:

Pathogenic/Likely pathogenic variants in DSP-encoded desmoplakin are strongly associated with arrhythmogenic cardiomyopathy (ACM). However, their contribution towards sinus node dysfunction has not been well-delineated. Case

summary:

A 74-year-old man with a pathogenic variant of DSP-encoded desmoplakin (c.478C >T; p.Arg160X) but no evidence of ACM presented with one episode of syncope in the setting of a gastrointestinal illness. Workup including echocardiography, cardiac magnetic resonance imaging, and Holter monitor did not show evidence of ACM or significant arrhythmias. One month later, he experienced several closely-spaced episodes of syncope associated with long sinus pauses and sinus arrest documented on telemetry. He underwent urgent dual chamber pacemaker implantation, during which a ventricular programmed stimulation study was performed and was negative for sustained ventricular arrhythmias. His syncopal episodes resolved and he had no recurrent events on three-month follow-up.

Discussion:

As highlighted here, DSP-encoded desmoplakin pathogenic/Likely pathogenic variants may contribute to isolated sinus node dysfunction. This clinical link should be further explored in larger studies involving patients with DSP variants.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article