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Background: Atrial standstill is a rare pathologic phenomenon characterized by absence of electrical and mechanical activity of one or both atria. SCN5A gene mutations are associated with a myriad of clinical cardiac phenotypes including sinus node dysfunction and atrial standstill.
Case Summary: We present a case of a 14-year-old boy who suffered acute embolic stroke in the setting of SNC5A-associated atrial standstill. The patient required thrombolysis and interventional thrombectomy, after which he recovered completely.
Discussion: To our knowledge, this is the first report of acute embolic stroke as the initial presentation of SCN5A-associated partial atrial standstill in the pediatric population. SCN5A-associated atrial standstill carries a significant risk of stroke and mortality in pediatric patients who are not identified and managed appropriately.
Take-home Messages: Atrial standstill can present with serious cardioembolic complications in pediatric patients. Prevention using oral anticoagulation should be considered in patients with partial atrial standstill, especially when associated with SCN5A variants and in the absence of atrial pacing.
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http://dx.doi.org/10.1016/j.jaccas.2025.104144 | DOI Listing |
JACC Case Rep
August 2025
Department of Research, Centre for Inherited Cardiovascular Diseases, IRCCS Foundation, University Hospital Policlinico San Matteo, Pavia, Italy.
Background: Atrial standstill is a rare arrhythmogenic disorder characterized by complete atrial electrical and mechanical inactivity. We report the 15th documented case of atrial dilated cardiomyopathy associated with the homozygous c.449G>A (p.
View Article and Find Full Text PDFJACC Case Rep
July 2025
Minneapolis Heart Institute, Allina Health, Minneapolis, Minnesota, USA.
Background: Atrial standstill is a rare pathologic phenomenon characterized by absence of electrical and mechanical activity of one or both atria. SCN5A gene mutations are associated with a myriad of clinical cardiac phenotypes including sinus node dysfunction and atrial standstill.
Case Summary: We present a case of a 14-year-old boy who suffered acute embolic stroke in the setting of SNC5A-associated atrial standstill.
JACC Case Rep
July 2025
Department of Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria. Electronic address:
Background: Myocarditis typically affects ventricles, whereas isolated atrial myocarditis is rare, causing conduction abnormalities, atrial standstill, and right heart failure.
Case Summary: Two weeks after a respiratory infection, a 35-year-old man developed dyspnea, leg edema, and bradycardia. Electrocardiogram revealed a narrow QRS escape rhythm without P waves, and N-terminal pro-B-type natriuretic peptide was elevated.
JACC Clin Electrophysiol
June 2025
Department of Cardiovascular Medicine, Institute of Science Tokyo, Tokyo, Japan.
Indian J Radiol Imaging
July 2025
Department of Imaging Sciences and Interventional Radiology, Sree Chitra Institute of Medical Sciences, Trivandrum, Kerala, India.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare inherited syndrome that affects muscles, joints, and the heart. The classic clinical triad includes early joint contractures, slowly progressive muscle weakness, and cardiac abnormalities. The common cardiac manifestations include conduction disturbances, systolic dysfunction, and dilated cardiomyopathy and may be associated with left ventricular noncompaction with an increased risk of thromboembolic events.
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