A5077492710- Cardiac Structural Anomalies and Repair
- Mechanical Circulatory Support Devices
- Cardiac Valve Diseases and Treatments
- Neurofibromatosis and Schwannoma Cases
- Sarcoma Diagnosis and Treatment
- Diabetic Foot Ulcer Assessment and Management
- Soft tissue tumor case studies
- Cardiac Imaging and Diagnostics
- RNA regulation and disease
University of Insubria
2022-2024
University of Parma
2023
Background Left ventricular free-wall rupture (LVFWR) is a catastrophic complication of acute myocardial infarction (AMI). Historically, cardiac surgery considered the treatment choice. However, because rarity this entity, little known regarding efficacy and safety surgical for post-infarction LVFWR. The aim study was to report single-center experience in field over period 30 years. Methods Patients who developed LVFWR following AMI underwent repair at our Institution from January 1990...
The finding of variants uncertain significance (VUS) in the activity a diagnostic genetic laboratory is common issue, which however provisional and needs to be periodically re-evaluated, due continuous advancements our knowledge diseases. Neurofibromatosis type 1, caused by occurrence heterozygous pathogenic NF1 variants, good model for studying evolution VUS, widespread use testing disease, constant enrichment international databases with full adult penetrance makes genotyping parents...
Left atrial dissection (LatD) is an exceedingly rare but serious complication of cardiac surgery. Its clinical presentation very different in individual cases. Surgical treatment for LatD often selected when the patient hemodynamically unstable; conservative treatments are commonly employed under stable conditions. We report a case after mitral valve replacement that was treated surgically with creation fenestration.
The finding of variants uncertain significance (VUS) in the activity a diagnostic genetic laboratory is common issue, which however provisional and needs to be periodically re-evaluated, due continuous advancements our knowledge diseases. Neurofibromatosis type 1, caused by occurrence heterozygous pathogenic NF1 variants, good model for studying evolution VUS, widespread use testing disease, constant enrichment international databases with full adult penetrance makes genotyping parents...