4 results match your criteria: "University of Padua. valeria.pergola@gmail.com.[Affiliation]"
Monaldi Arch Chest Dis
September 2023
The Heart Centre, King Faisal Specialist Hospital and Research Center, Riyadh; College of Medicine, Alfaisal University, Riyadh.
Nowadays, the diagnosis of cardiac myxomas (CM), particularly the histological types, remains a challenge. Two-dimensional (2D) transthoracic (TT) and transesophageal (TEE) echocardiography (ECHO) represent the first steps in the imaging pathway. 3D ECHO, implemented in imaging practice, appears to be an emerging diagnostic technique that overcomes some of the limitations of 2D ECHO while integrating the information provided by magnetic resonance (MRI).
View Article and Find Full Text PDFMonaldi Arch Chest Dis
August 2023
Heart Center, King Faisal Specialist Hospital and Research Center, Riyadh.
The authors report a case of a patient with a history of immunoglobulin A nephropathy who, during the admission for pneumonia, had an incidental finding of a huge mitral valve (MV) mass on transthoracic echocardiography. The differential diagnosis was challenging because the clinical scenario raised the suspicion of possible infective endocarditis, and the imaging features were suggestive of a myxoma or vegetation. The patient underwent urgent excision of the mass with MV replacement due to the high risk of embolism.
View Article and Find Full Text PDFMonaldi Arch Chest Dis
October 2021
Department of Medicine, Institute of Radiology, University of Padua.
SCA from the right sinus is the rarest coronary anomaly. We describe 2 cases: 1 with SCA type-1RI; 2 with SCA type-2RII-A. Appropriate and successful treatment (CABG in case-1; PTCA in case-2) was chosen relying on accurate morphological description provided by MDCT, in order to recognize all the possible mechanisms of myocardial ischemia.
View Article and Find Full Text PDFMonaldi Arch Chest Dis
August 2021
Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua.
Mucopolysaccharidoses, a rare inherited disorder of lysosomal storage, account for less than 0.1% of all genetic diseases. The penetrance is highly variable and clinically it varies from severe fetal-neonatal forms to attenuated diseases diagnosed in adult individuals.
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