Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Radiological insights into fibromuscular dysplasia unveiled by intracranial aneurysms and iliac vein hypoplasia in suspected DVT.
Radiol Case Rep
March 2025
Radiology Department, University Hospital Center of Souss Massa, Faculty of Medicine and Pharmacy, Ibn Zohr Agadir University, Agadir, Morocco.
Fibromuscular Dysplasia (FMD) is a nonatherosclerotic, noninflammatory vascular disorder predominantly affecting women aged 18 to 65 years. This case report highlights a 74-year-old female diagnosed with FMD incidentally during evaluation for deep vein thrombosis (DVT). Imaging revealed significant vascular anomalies, including a giant intracranial carotid aneurysm and a hypoplastic iliac vein with extensive collateral formation.
View Article and Find Full Text PDFPreoperative Computed Tomography Virtual Simulation for HeartMate 3 Implantation in Small Children.
Ann Thorac Surg Short Rep
September 2024
Department of Cardiovascular Surgery, Tokyo Women's Medical University, The Heart Institute of Japan, Tokyo, Japan.
An implantable ventricular assist device became smaller and has been used for small body size patients. However, it is still challenging to determine whether it is implantable for pediatric patients. The preoperative computed tomography virtual simulation provided spatial information among the pump, intracardiac structures, and extracardiac structures, which was very useful to assess the implantability for borderline children.
View Article and Find Full Text PDFIntraoperative Type B Aortic Dissection With Malperfusion in a Patient With Marfan Syndrome.
Ann Thorac Surg Short Rep
June 2024
Department of Cardiothoracic Surgery, St Francis Hospital, Roslyn, New York.
We present the case of a 72-year-old man diagnosed with an aortic root aneurysm who was then diagnosed with Marfan syndrome. The patient suffered an intraoperative type B dissection with lower extremity malperfusion managed with an axillary-bifemoral extra-anatomic bypass.
View Article and Find Full Text PDFOrthotopic Heart Transplantation in a Patient With Hypertrophic Cardiomyopathy and Marfan Syndrome.
Ann Thorac Surg Short Rep
June 2024
Division of Cardiac Surgery, Northwestern University Feinberg School of Medicine and Northwestern Medicine, Chicago, Illinois.
A 24-year-old man with Marfan syndrome and heart failure from hypertrophic cardiomyopathy was referred to our institution in cardiogenic shock for advanced therapies. He was supported by a femoral intra-aortic balloon pump, then bridged to orthotopic heart transplantation. This is a report of an orthotopic heart transplantation in a patient with both Marfan syndrome and heart failure from hypertrophic cardiomyopathy.
View Article and Find Full Text PDFBentall Procedure in a Marfan Syndrome Patient With Reduced Ejection Fraction: A Case Report.
Cureus
December 2024
Department of Cardiac Surgery, King Fahad University Hospital, Dammam, SAU.
Article Synopsis
- Marfan syndrome (MFS) is a genetic disorder that affects connective tissue and often results in serious heart issues like aortic dilation and aneurysms.
- A 35-year-old woman from Bangladesh with MFS experienced severe chest pain and had a significant aortic root aneurysm, leading to a dangerously low ejection fraction of 20%-25%.
- An urgent Bentall procedure was performed to address the aortic dilation, which improved her condition, as her ejection fraction increased to 25% by the time she was discharged.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!