Atrioventricular septal defect associated with noncompacted myocardium

doi:10.15406/jccr.2015.02.00083

Journal of

eISSN: 2373-4396

Cardiology & Current Research

Case Report Volume 2 Issue 6

Atrioventricular septal defect associated with noncompacted myocardium

Silvia Iancovici,¹

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George Giannakoulas,² Stelios Paraskevaidis,² George Spanos,³ Haralambos Karvounis²

¹Cardiology Department, Clinic Emergency Hospital of Bucharest, Romania
²Cardiology Department, AHEPA University Hospital, Greece
³Radiology Department, Greece

Correspondence: Silvia Iancovici, Cardiology Department, Clinic Emergency Hospital of Bucharest, Calea Floreasca No. 8, Sector 1, 014461 Bucharest, Romania, Tel 004021 5992300

Received: February 25, 2015 | Published: June 1, 2015

Citation: Iancovici S, Giannakoulas G, Paraskevaidis S, et al. Atrioventricular septal defect associated with noncompacted myocardium. J Cardiol Curr Res. 2015;2(6):119-122. DOI: 10.15406/jccr.2015.02.00083

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Abstract

The presented case conveys two significant clinical messages. Firstly, the embolic risk for patients with non-compacted myocardium is high and anticoagulants should be prescribed in case of left ventricular dysfunction or atrial fibrillation even if the CHA2DS2-VASc score is low. Secondly, the presence of ventricular arrhythmias in a patient with congenital heart disease and preserved biventricular function should lead to search for other causes of enhanced arrhythmic substrate, such as non-compacted myocardium.

Keywords: non-compacted myocardium, ventricular arrhythmias

Case study

A 41 year-old-woman was admitted to our hospital for symptomatic complete atrioventricular block and atrial fibrillation. The patient had previously been diagnosed during childhood with partial atrioventricular septal defect and pulmonary valve stenosis; she had undergone at age 19 patch closure of primum ASD, repair of the left atrioventricular valve and open pulmonary valvotomy. She had a history of embolism in her right popliteal artery 10 years before admission for which she has been treated with oral anticoagulation. At admission, blood analyses including electrolytes were normal. Transthoracic echocardiography revealed a normal-sized left ventricle with good systolic function, increased left ventricular wall thickness and typical prominent trabeculations and intertrabecular recesses in the mid and apical segments of lateral and inferior wall pathognomonic for non-compacted myocardium (Figure 1A). Color Doppler imaging of the loosened myocardium demonstrated blood flow throughout the trabeculations (Figure 1B). Right ventricle was also mildly trabeculated with normal dimensions and preserved systolic function. There was no residual atrial shunt and there was mild left atrioventricular valve regurgitation and mild pulmonary valve stenosis. Cardiac MRI confirmed the diagnosis of left ventricular non-compaction with preserved left ventricular function, but also demonstrated the significant involvement of right ventricular myocardium (Figure 2).

Figure 1A Four-chamber echocardiographic view showing increased wall thickness in the left ventricular apical segments.

Figure 1B Parasternal short-axis echocardiographic view showing the typical prominent trabeculations and intertrabecular recesses (left) and how the color enters the intertrabecular recesses (right, white arrows).

Figure 2 Four-chamber steady-state free precession (SSFP) cine image showing biventricular noncompaction at mid and apical levels.

A 24-hour Holter monitoring performed 3 months before admission documented episodes of non-sustained ventricular tachycardia and, therefore, she underwent an electrophysiological study before the implantation of a cardioverter-defibrillator (ICD). A ventricular tachycardia followed by ventricular fibrillation was induced and an ICD was implanted. Two years after ICD implantation the patient experienced an episode of sustained ventricular tachycardia converted with antitachycardia pacing (Figure 3). Noncompaction of the left ventricular myocardium is a rare condition thought to be determined by intrauterine arrest of compaction of the loose interwoven meshwork that gives rise to the fetal myocardial fibers.¹ The disease uniformly affects the left ventricle, but biventricular involvement has frequently been reported. Noncompaction of the left ventricle has been described as an isolated cardiomyopathy but may also be encountered in association with other abnormalities, such as congenital heart disease and neuromuscular disease.² Left or right ventricular outflow tract obstruction, atrioventricular valve abnormalities and conotruncal lesions are the most common congenital heart lesions that are associated with non-compacted myocardium.³ The main clinical manifestations of non-compacted myocardium are arrhythmias, heart failure due to left ventricular systolic dysfunction and embolism.^3,4 Management of these patients should be tailored based on these complications.

Figure 3 ICD recording showing the episode of ventricular tachycardia. Both channels record ventricular (V) electrograms. ATP: Antitachycardia pacing.