Double Outlet Right Ventricle with Discordant Atrioventricular Connections in a Newborn:Case Report and Brief Overview of the Literature
Küçük Resim Yok
Tarih
2016
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Çift çıkışlı sağ ventrikül bütün doğumsal kalp defektlerinin nadir bir kardiyak malformasyondur. Anormal ventriküloarteryal bağlantıların heterojen bir grubudur. Her iki büyük arter (pulmoner arter ve aorta) esas olarak morfolojik sağ ventrikülden çıkmaktadır. Diskordan atriyoventriküler bağlantılı çift çıkışlı sağ ventrikül ve hipoplazik pulmoner arterleri olan bir yenidoğanı sunmaktayız. Ekokardiyografi ile tanı konulan nadir karmaşık bir kardiyak malformasyonu bildirdik. Ekokardiyografi ile segmental yaklaşım ve kardiyak segmentlerin ardışık analizi karmaşık kardiyak malformasyonların tanısında ipucudur.
Double outlet right ventricle is a rare cardiac malformation of all congenital cardiac defects. It is a heterogeneous group of abnormal ventriculoarterial connections. Both great arteries (pulmonary artery and aorta) arise primarily from the morphological right ventricle. Double outlet right ventricle with discordant atrioventricular connections have been reported rarely in the literature. We report a newborn with double outlet right ventricle with discordant atrioventricular connections and hypoplastic pulmonary arteries. We reported a rare complex cardiac malformation diagnosed by echocardiography. Segmental approach and sequential analysis of cardiac segments by echocardiography are the clue for diagnosis of complex cardiac malformations.
Double outlet right ventricle is a rare cardiac malformation of all congenital cardiac defects. It is a heterogeneous group of abnormal ventriculoarterial connections. Both great arteries (pulmonary artery and aorta) arise primarily from the morphological right ventricle. Double outlet right ventricle with discordant atrioventricular connections have been reported rarely in the literature. We report a newborn with double outlet right ventricle with discordant atrioventricular connections and hypoplastic pulmonary arteries. We reported a rare complex cardiac malformation diagnosed by echocardiography. Segmental approach and sequential analysis of cardiac segments by echocardiography are the clue for diagnosis of complex cardiac malformations.
Açıklama
Anahtar Kelimeler
Genel ve Dahili Tıp
Kaynak
Journal of Clinical and Analytical Medicine
WoS Q Değeri
Scopus Q Değeri
Cilt
7
Sayı
1