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Case Reports
. 2024 Feb 14;16(2):e54222.
doi: 10.7759/cureus.54222. eCollection 2024 Feb.

Late-Onset Dilated Cardiomyopathy in Auto Immune-Mediated Complete Congenital Heart Block: A Case Report

Affiliations
Case Reports

Late-Onset Dilated Cardiomyopathy in Auto Immune-Mediated Complete Congenital Heart Block: A Case Report

Amulya Dharmagadda et al. Cureus. .

Abstract

Complete congenital heart block (CHB), a rare and fatal bradyarrhythmia observed in children, carries significant mortality and morbidity. When congenital heart block occurs in isolation with a structurally normal heart, it prompts suspicion of an autoimmune etiology, wherein maternal antibodies are transmitted transplacentally, impacting the fetal conducting system. The manifestation of congenital complete atrioventricular block (CCAVB) can lead to complications such as dilated cardiomyopathies, arrhythmias, and fibroelastosis in certain cases. Notably, dilated cardiomyopathy is a significant prognostic factor in children diagnosed with congenital heart block. Pathological investigations have revealed the presence of antibodies, complements, and indicators of inflammation or fibrosis across the myocardium, emphasizing the shared molecular mechanisms between CCAVB and the development of dilated cardiomyopathy (DCM). This article presents the case of a one-year-old female child who presented with signs of dilated cardiomyopathy, later identified through retrospective evaluation as having autoimmune congenital heart block. The mother of the child was diagnosed with Sjogren's syndrome, characterized by positive anti-RO titers. Remarkably, the child remained asymptomatic for a year without the need for pacing intervention. The child's condition was successfully stabilized with appropriate treatment, and plans for pacemaker insertion will be considered once specific criteria are met. The onset of cardiomyopathy in a known case of CCAVB should serve as a crucial alert for prognostic considerations and the potential necessity for early-pacing intervention.

Keywords: atrioventricular block; congenital heart block; dilated cardiomyopathy; pediatrics & neonatology; sjogren's.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. ECG showing complete congenital heart block
Black arrows indicate P waves, and orange arrows indicate QRS complexes, which are independent of P waves.

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References

    1. Congenital and childhood atrioventricular blocks: pathophysiology and contemporary management. Baruteau AE, Pass RH, Thambo JB, et al. Eur J Pediatr. 2016;175:1235–1248. - PMC - PubMed
    1. Congenital heart block: development of late-onset cardiomyopathy, a previously underappreciated sequela. Moak JP, Barron KS, Hougen TJ, et al. J Am Coll Cardiol. 2001;37:238–242. - PubMed
    1. Congenital heart block in neonatal lupus: the pediatric cardiologist's perspective. Friedman DM, Rupel A, Glickstein J, Buyon JP. Indian J Pediatr. 2002;69:517–522. - PubMed
    1. Pregnancy outcomes in patients with autoimmune diseases and anti-Ro/SSA antibodies. Brucato A, Cimaz R, Caporali R, Ramoni V, Buyon J. Clin Rev Allergy Immunol. 2011;40:27–41. - PMC - PubMed
    1. Kashou AH, Goyal A, Nguyen T, Ahmed I, Chhabra L. Kashou AH, Goyal A, Nguyen T, Ahmed I, Treasure Island (FL): StatPearls Publishing; 2023. Atrioventricular Block; p. 2023.

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