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Hydrops Fetalis Secondary to Left Ventricle Diastolic Collapse Caused by Giant Rhabdomyoma: Utility of 4D STIC and Fetal Heart Quantification Techniques.
Echocardiography
March 2025
Department of Obstetrics & Gynaecology, Annai Velankanni Multispeciality Hospital, Tirunelveli, Tamilnadu, India.
This case image illustrates the utility of fetal HQ and 4D STIC echocardiography in a 24-week gestation fetus in understanding the hemodynamics responsible for the fetal heart failure due to LV rhabdomyoma.
View Article and Find Full Text PDFASSESSMENT OF ECHOCARDIOGRAPHIC PARAMETERS IN HEALTHY FREE-RANGING GIANT ANTEATERS ().
J Zoo Wildl Med
March 2025
Faculdade de Medicina Veterinária (FAVET), Universidade Federal de Mato Grosso (UFMT), Brazil.
The aim of this study was to conduct Doppler echocardiography on healthy free-ranging anteaters () and to evaluate the relationship between echocardiographic parameters of diagnostic importance and animal body weight (BW). This work utilized 8 anesthetized adult animals and 4 manually restrained pups. The echocardiographic examinations were performed with the animal in left lateral recumbency.
View Article and Find Full Text PDFSolitary Fibrous Tumor of the Pleura: A Clinical Case of a Giant Malignant Tumor With Post-surgical Recurrence.
Cureus
February 2025
Thoracic Surgery, Mohammed VI University Hospital, Marrakesh, MAR.
Solitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor, making up a small fraction of primary pleural tumors. It is typically benign but can display malignant features. This case presents a 59-year-old patient with a giant malignant SFTP located in the right posterior inferior mediastinum, which caused significant compression of adjacent structures, including the lung, heart, and esophagus.
View Article and Find Full Text PDFCoronary Arteries Involvement in Giant Cell Arteritis Diagnosis Using 2-[18F]FDG-PET/CT.
Clin Nucl Med
March 2025
Nantes Université, Univ Angers, CHU Nantes, INSERM, CNRS, CRCI2NA, Médecine Nucléaire.
Coronary artery involvement in giant cell arteritis (GCA) is rare but can lead to severe complications, including myocardial infarction and death. We present unique 2-[18F]fluorodeoxyglucose positron emission tomography/computed tomography (2-[18F]FDG-PET/CT) findings in a 91-year-old woman with GCA. In addition to typical aortic and supra-aortic involvement, this scan revealed intense FDG uptake in the coronary arteries, including the left main trunk, left anterior descending, circumflex, and right coronary arteries.
View Article and Find Full Text PDFMarfan syndrome cardiomyocytes show excess of titin isoform N2BA and extended sarcomeric M-band.
J Gen Physiol
May 2025
Department of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Marfan syndrome (MFS) is an autosomal dominant disease caused by mutations in the gene (FBN1) of fibrillin-1, a major determinant of the extracellular matrix (ECM). Functional impairment in the cardiac left ventricle (LV) of these patients is usually a consequence of aortic valve disease. However, LV passive stiffness may also be affected by chronic changes in mechanical load and ECM dysfunction.
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