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An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis

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dc.contributor.author Elkıran, Özlem
dc.contributor.author Karakurt, Cemşit
dc.contributor.author İnce, Damla
dc.date.accessioned 2020-07-01T11:47:09Z
dc.date.available 2020-07-01T11:47:09Z
dc.date.issued 2019
dc.identifier.citation Özlem E., Cemsit K., Damla İ. (2019). An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis, Erciyes Medical Journal, İnönü Üniversitesi, Malatya. tr_TR
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/16264
dc.description.abstract Öz:Rhabdomyomas are the most common primary cardiac tumors in infants and children. They are usually associated with tuberous sclerosis (TS). As the tumors tend to regress spontaneously, surgical intervention is not usually performed unless they become obstructive or cause incessant arrhythmias. We report an extremely rare case of rhabdomyoma serving as a substrate for Wolff-Parkinson-White (WPW) syndrome and intractable supraventricular tachycardia accompanied by TS. Our case is particularly interesting because it was diagnosed prenatally. The signs of WPW syndrome disappeared from the electrocardiogram with the regression of the tumor. tr_TR
dc.language.iso en tr_TR
dc.publisher Erciyes Medical Journal tr_TR
dc.subject Genel ve Dahili Tıp tr_TR
dc.title An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis tr_TR
dc.type Article tr_TR


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