Objective: To study the diagnostic significance of computed tomography (CT) in atrial isomerism.
Method: In one of the 2 cases of left atrial isomerism, abdominal CT scan with and without contrast enhancement were both performed, the other had plain thoraco-abdominal CT scan, and another case of right atrial isomerism received thoraco-abdominal contrast enhanced scan and thin-slice scan of the trachea. The diagnoses of all the 3 cases were surgically and pathologically confirmed.
Result: In the CT images of the 2 cases of left atrial isomerism, some typical features were identified including bilaterally symmetric bronchi, levoversion of the heart, horizontally positioned liver, absence of hepatic segment of the inferior vena cava and dilated azygos, short pancreas and double spleen, and mirror image isomerism of the major arteries and abdominal organs. The case of right atrial isomerism had bilateral upper lobe tracheal bronchus, mirror image isomerism of the heart and abdominal organs, short pancreas, translocation of the inferior vena cava to the left of the abdominal aorta, both of which were on the left of the spine.
Conclusions: CT have distinct diagnostic value in revealing thoraco-abdominal organs and major vessels, which can be crucial in the diagnosis and surgical management of patients with atrial isomerism.
Download full-text PDF |
Source |
---|
Cardiol Young
November 2024
Department of Paediatric Cardiology, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Aim: This study aims to evaluate the clinical characteristics and outcomes of children diagnosed with sinus node dysfunction.
Methods: This was a retrospective review of patients diagnosed with sinus node dysfunction in two tertiary paediatric cardiology centres in Turkey from January 2011 to June 2022.
Results: In all, 77 patients (50, 64.
Cureus
October 2024
Anesthesiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Dr. D.Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Coarctation of the aorta (CoA) accounts for a small percentage of all congenital heart diseases (CHD) and occurs with a rare incidence in live births. It is a frequently diagnosed cardiac defect in infancy, though some patients present later with severe complications and reduced life expectancy. Heterotaxy syndrome is marked by abnormal lateralization of abdominal and thoracic organs, including the cardiac atria.
View Article and Find Full Text PDFPacing Clin Electrophysiol
December 2024
Department of Pediatric Electrophysiology, Osaka City General Hospital, Miyakojima-ku, Osaka, Japan.
J Ultrasound Med
October 2024
Division of Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Objective: This study compared the accuracy of prenatal congenital heart disease (CHD) diagnosed by maternal-fetal medicine specialists (MFMs) and pediatric cardiologists (PCs), using postnatal cardiac findings as the reference standard.
Methods: This retrospective analysis at Siriraj Hospital, Bangkok, Thailand, involved 125 pregnancies with fetal CHD diagnosed by MFMs and evaluated by PCs later. Prenatal CHD diagnoses by either MFM or PC were compared with postnatal diagnoses obtained through echocardiography, cardiac surgery/catheterization, or autopsy.
Asian Cardiovasc Thorac Ann
November 2024
Department of Cardiovascular Surgery, Miyagi Children's Hospital, Sendai, Japan.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!