Key result
Juvenile neuronal ceroid-lipofuscinosis links to apical LV noncompaction and HCM on echocardiography.
Why the study?
Juvenile neuronal ceroid-lipofuscinosis is a rare progressive hereditary disease in which cardiac involvement is not well known, and longer survival likely increases the incidence of cardiac complications.
Suggests possible echocardiography surveillance in juvenile neuronal ceroid-lipofuscinosis; hypothesis-generating and requires validation in larger cohorts.
We report a 17-year-old female with juvenile neuronal ceroid-lipofuscinosis (NCL) accompanied by hypertrophic cardiomyopathy (HCM) and left ventricular noncompaction (LVNC). Within our knowledge, this is the first reported case of juvenile NCL with LVNC, and the youngest case of HCM diagnosed by ultrasound. Juvenile NCL is a progressive hereditary disease involving multi-organ accumulation of ceroid-lipofuscin; its resulting complications require prompt attention. Due to its relative rarity, its cardiac involvement is not well known. Based on findings from this patient and related juvenile NCL cases, the risk of cardiac involvement tends to increase with age; a high frequency of ventricular hypertrophy has been reported in patients aged older than 20 years of age. Medical progress and comprehensive care have led to longer survival in patients with juvenile NCL, which likely increases the incidence of cardiac involvement. In relation to HCM in other metabolic disorders, attention should be paid to arrhythmias, including repolarization disturbances, sinus node dysfunction and ventricular tachycardia. LVNC is a cardiomyopathy characterized by prominent left ventricular trabeculae and deep intratrabecular recesses, which are associated with diastolic or systolic dysfunction, thromboembolic complications and arrhythmias. From ours and other case reports, we recommend regular follow-up of NCL patients as follows: echocardiography to estimate cardiomyopathy, Holter monitoring to identify arrhythmias, and computed tomography to detect thrombosis from both ventricles. The mechanism of the HCM and LVNC associated with juvenile NCL remains unclear. Our case requires careful follow-up. Prospective studies of the cardiac involvement in juvenile NCL are necessary to further elucidate its pathomechanism.
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Murata et al. (2015) conducted a letter in Juvenile neuronal ceroid-lipofuscinosis with hypertrophic cardiomyopathy and left ventricular noncompaction (n=1). Echocardiography and clinical/family screening was evaluated on Left ventricular noncompaction (NC/C ratio) and cardiac complications. Echocardiography in a juvenile neuronal ceroid-lipofuscinosis patient confirmed apical LV noncompaction (NC/C ratio >=2) and HCM, with no cardiac abnormalities found in family members.
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