European journal of pediatrics · 2013
Persistent multifocal atrial tachycardia in infant with encephalocraniocutaneous lipomatosis: a case report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Pregowska Katarzyna, Jurkiewicz Elzbieta, Miszczak-Knecht Maria, Turska-Kmiec Anna, Bieganowska Katarzyna
Аннотация
UNLABELLED: Encephalocraniocutaneous lipomatosis (ECCL, Haberland syndrome, Fishman syndrome) is a very rare congenital disorder, involving skin, eye, bone and central nervous system malformations. In this paper we present a case of a 2-month-old boy with encephalocraniocutaneous lipomatosis diagnosed on the basis of characteristic clinical manifestations and neuroimaging findings. Neurologically, the child presented only with mild physical and mental retardation. 24-h Holter monitoring revealed asymptomatic multifocal atrial tachycardia. Initial therapy with digoxin and metoprolol was not effective. Introduction of propafenone resulted in supression of supraventricular arrhythmia. During the 3- years follow-up, sinus rhythm persisted, but neurological status deteriorated.
CONCLUSION: Supraventricular arrhythmia may be associated with Haberland syndrome. It seems that propafenone is most effective in this condition.
CONCLUSION: Supraventricular arrhythmia may be associated with Haberland syndrome. It seems that propafenone is most effective in this condition.