scholarly journals VENTRICULAR SEPTAL DEFECT WITH SEVERE AORTIC REGURGITATION, SUB AORTIC STENOSIS, AORTIC AND PULMONARY ROOTS DILATION IN AN ADULT: A CASE REPORT

2020 ◽  
Vol 53 (1) ◽  
Author(s):  
Deebaj Nadeem ◽  
Abdul Mueed ◽  
Parveen Akhtar
Keyword(s):  
Case Report ◽  
Aortic Stenosis ◽  
Ventricular Septal Defect ◽  
Aortic Regurgitation ◽  
Septal Defect ◽  
Severe Aortic Regurgitation

scholarly journals Redo Bentall’s Procedure for Annuloaortic Ectasia with Severe Aortic Regurgitation: A Video Presentation

2019 ◽  
Vol 03 (01) ◽  
pp. 39-41
Author(s):  
Lakshmi Kumari Sankhyan ◽  
Ujjwal K. Chowdhury ◽  
Niwin George ◽  
Sukhjeet Singh ◽  
Vasubabu Gudala ◽  
...  
Keyword(s):  
Ventricular Septal Defect ◽  
Aortic Regurgitation ◽  
Aortic Root ◽  
Septal Defect ◽  
Mechanical Valve ◽  
Composite Graft ◽  
Aortic Root Replacement ◽  
Annuloaortic Ectasia ◽  
Video Presentation ◽  
Severe Aortic Regurgitation

AbstractA 25-year old female patient with repaired ventricular septal defect and aortic valvular reconstruction underwent successful aortic root replacement using a composite graft with mechanical valve.

scholarly journals Unruptured Aneurysm of Sinus of Valsalva Coexisting with the Large Ventricular Septal Defect and Severe Aortic Regurgitation in a Young Man

2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Pouya Nezafati ◽  
Mohammad Hassan Nezafati ◽  
Hamid Hoseinikhah
Keyword(s):  
Ventricular Septal Defect ◽  
Aortic Regurgitation ◽  
Septal Defect ◽  
Mechanical Valve ◽  
Valve Prosthesis ◽  
Sinus Of Valsalva ◽  
Severe Aortic Regurgitation ◽  
Risk Of Mortality ◽  
Limb Edema

Introduction. Unruptured sinus of valsalva aneurysm (SVA) is a rare congenital anomaly, particularly, when it coexists with a ventricular septal defect (VSD) and aortic regurgitation due to the prolapse of the elongated aortic cusp into the VSD. In this report, we present the case of a 19-year-old young man with VSD challenging in spite of dyspnea and lower limb edema.Presentation of Case. Its diagnosis was made on the basis of transthoracic echocardiography results. Surgical management consisted of replacing the SVA with mechanical valve prosthesis. A Gore-Tex patch repaired the VSD.Discussion. In the follow-up periods, clinical and echocardiographic tests showed that the patient was in excellent status.Conclusion. SVA requires a surgical procedure due to its high risk of mortality in unoperated patients and a good safety of surgery.

scholarly journals Takotsubo syndrome after palliative transcatheter treatment of acquired aortic stenosis in patient with congenital ventricular septal defect. Case report

2021 ◽  
Vol 93 (9) ◽  
pp. 1078-1085
Author(s):  
Alexey E. Komlev ◽  
Marina D. Muksinova ◽  
Marina A. Saidova ◽  
Ella V. Kurilina ◽  
Timur E. Imaev
Keyword(s):  
Case Report ◽  
Aortic Valve ◽  
Aortic Stenosis ◽  
Ventricular Septal Defect ◽  
Transcatheter Aortic Valve Replacement ◽  
Clinical Case ◽  
Septal Defect ◽  
Severe Aortic Stenosis ◽  
Takotsubo Syndrome ◽  
Transcatheter Aortic Valve

The authors report the clinical case of secondary Takotsubo syndrome developed after transcatheter aortic valve replacement that was performed in compassionate manner in female patient with combination of congenital ventricular septal defect and acquired severe aortic stenosis. In the teams view, Takotsubo syndrome was triggered with profound changes of intracardial hemodynamics subsequent to iatrogenic impairment of preexisting interventricular shunt.

Management of Platelets in a Persian Girl with the Tetralogy_Pantalogy of Fallot (Tof_Pof): A Case Report Study

2020 ◽  
Author(s):  
Bahram Alamdary Badlou
Keyword(s):  
Case Report ◽  
Ventricular Septal Defect ◽  
Atrial Septal Defect ◽  
Sleep Disorders ◽  
Social Life ◽  
Rare Case ◽  
Septal Defect ◽  
Old Persian ◽  
Underlying Mechanisms ◽  
The Relationship

We report a rare case of unrepaired Tetralogy_Pantalogy of Fallot (TOF_POF) in a 20 years old Persian girl Mrs Zeynab S., who presented with cyanotic finger tops appearance, ongoing chronic thrombolytic destruction processes, and remarkable thrombocytopenia [1,2], heart ventricular septal defect (VSD), and might atrial septal defect (ASD), anxiety, sleep disorders, nightmares, and limited social life. Additionally, the relationship between underlying mechanisms, possible treatments of the thrombocytopenia, erythrocytosis, and unrepaired cardiovascular leakages remains unknown.

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