An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis
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 rep...
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2019-03-01
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doaj-432af43e61b343338cb3aaafc212ecee2021-01-24T18:15:54ZengKARE PublishingErciyes Medical Journal2149-22472019-03-0141110811010.14744/etd.2018.18165EMJ-96646An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous SclerosisÖzlem Elkıran0Cemşit Karakurt1Damla İnce2Department of Pediatric Cardiology, İnonu University Faculty of Medicine, Malatya, TurkeyDepartment of Pediatric Cardiology, İnonu University Faculty of Medicine, Malatya, TurkeyDepartment of Pediatric Cardiology, İnonu University Faculty of Medicine, Malatya, TurkeyRhabdomyomas 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.https://jag.journalagent.com/z4/download_fulltext.asp?pdir=erciyesmedj&un=EMJ-96646wolff-parkinson-white syndromechildrhabdomyoma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Özlem Elkıran Cemşit Karakurt Damla İnce |
spellingShingle |
Özlem Elkıran Cemşit Karakurt Damla İnce An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis Erciyes Medical Journal wolff-parkinson-white syndrome child rhabdomyoma |
author_facet |
Özlem Elkıran Cemşit Karakurt Damla İnce |
author_sort |
Özlem Elkıran |
title |
An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis |
title_short |
An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis |
title_full |
An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis |
title_fullStr |
An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis |
title_full_unstemmed |
An Extremely Rare Cause of Wolff-Parkinson-White Syndrome: Rhabdomyoma in Association With Tuberous Sclerosis |
title_sort |
extremely rare cause of wolff-parkinson-white syndrome: rhabdomyoma in association with tuberous sclerosis |
publisher |
KARE Publishing |
series |
Erciyes Medical Journal |
issn |
2149-2247 |
publishDate |
2019-03-01 |
description |
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. |
topic |
wolff-parkinson-white syndrome child rhabdomyoma |
url |
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=erciyesmedj&un=EMJ-96646 |
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