Two cardiomyopathies in one heart
Yazarlar (1)
Prof. Dr. Onur ŞAHİN Sinop Üniversitesi, Türkiye
Makale Türü Özgün Makale (Uluslararası alan indekslerindeki dergilerde yayınlanan tam makale)
Dergi Adı Echocardiography
Makale Dili Basım Tarihi 01-2006
Cilt / Sayı / Sayfa 23 / 6 / 519–521 DOI
Makale Linki https://www.academia.edu/download/53953745/j.1540-8175.2006.00253.x20170723-2872-xpc2mc.pdf
UAK Araştırma Alanları
Yoğun Madde Fiziği
Özet
A 25-year-old male patient with the diagnosis of arrhythmogenic right ventricular dysplasia (ARVD) and recurrent syncope was referred to our institute for implantation of an implantable cardioverter defibrillator (ICD). Electrocardiography showed T-wave inversion in the right precordial leads and a ventricular premature beat with left bundle branch block morphology (Fig. 1). Holter monitor recordings revealed runs of sustained ventricular tachycardia originating from the right ventricle (RV). Transthoracic echocardiography (TTE) showed RV dilatation with reduced ejection fraction, dyskinesia, and severely attenuated systolic thickening in its free wall. The TTE was also remarkable for the presence of diagnostic features of ventricular noncompaction (VNC), characteristically including a compacted epicardial layer and a noncompacted endocardial layer that consisted of a prominent trabecular meshwork and deep intertrabecular recesses filled with blood from the ventricular cavity in the apical and mid portions of the left ventricle (LV). LV systolic function was preserved. Additionally, an
Anahtar Kelimeler
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Google Scholar 11

Paylaş