Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Channabasavaraj S Hiremath"'
Autor:
Channabasavaraj S Hiremath, Utkarsh Sanghavi, Aditya N Doddamane, Anuradha Kamath, Shekhar Rao
Publikováno v:
Annals of Pediatric Cardiology, Vol 13, Iss 2, Pp 160-162 (2020)
Lymphangiomas are relatively uncommon lesions of the lymphatic channels which can arise in virtually any part of the body. Although the most common site is the head/neck region, they could be found in the mediastinum. If mediastinal lymphangiomas are
Externí odkaz:
https://doaj.org/article/d5453ea2eea24b81ad8b4f6e603c159d
Autor:
Anitha Diwakar, Sathya Swaroop Patnaik, Channabasavaraj S Hiremath, Kolli S Chalam, Parvatkumar Dash
Publikováno v:
Annals of Cardiac Anaesthesia, Vol 22, Iss 1, Pp 24-29 (2019)
Background: We reviewed our experience with ruptured sinus of Valsalva aneurysms (RSOV) to determine a correlation with preexisting heart failure (HF) and coexisting cardiac lesions (aortic regurgitation [AR] and ventricular septal defect [VSD]) to p
Externí odkaz:
https://doaj.org/article/0e1df5d11afb4c04b4449cdd5dbb2c0b
Publikováno v:
Annals of Cardiac Anaesthesia, Vol 23, Iss 1, Pp 98-99 (2020)
Aorto-left ventricular tunnel (ALVT) is a rare congenital anomaly with extracardiac channel connecting ascending aorta to the ventricle. It presents early in life due to congestive cardiac failure. We present a case of ALVT with unusual morphology in
Externí odkaz:
https://doaj.org/article/6b9dcdbd4d434e6495372343a064e496
Publikováno v:
Cardiology in the Young. :1-3
Transcatheter device closure has emerged as the preferred treatment for ostium secundum atrial septal defects with adequate margins, occasionally requiring surgical intervention to manage complications. We report a case of a young female patient who
Publikováno v:
Journal of Cardiac Surgery. 37:3016-3025
Patient prosthesis mismatch is a real problem observed in patients receiving aortic valves too small for their body surface area. This situation is entirely preventable with the apt use of root augmentation procedures. This study aims to evaluate and
Publikováno v:
European Journal of Cardio-Thoracic Surgery. 63
Publikováno v:
Cardiology in the Young. 31:1502-1503
Publikováno v:
Annals of Cardiac Anaesthesia
Annals of Cardiac Anaesthesia, Vol 23, Iss 1, Pp 98-99 (2020)
Annals of Cardiac Anaesthesia, Vol 23, Iss 1, Pp 98-99 (2020)
Aorto-left ventricular tunnel (ALVT) is a rare congenital anomaly with extracardiac channel connecting ascending aorta to the ventricle. It presents early in life due to congestive cardiac failure. We present a case of ALVT with unusual morphology in
Publikováno v:
Interactive CardioVascular and Thoracic Surgery. 29:805-807
We describe a case of a 46-year-old man with calcified amorphous tumour in the right atrium and significant coronary artery disease. Preoperative investigations revealed a polypoid oscillating mass arising from the interatrial septum and attached to
Autor:
Channabasavaraj S Hiremath, Anuradha Kamath, Siddharth Amboli, Yatindra U. Ashtaputre, Krishna Manohar
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 11:NP210-NP212
Partial anomalous pulmonary venous return is a congenital anomaly in which some of the pulmonary veins drain into the right atrium or one of its venous tributaries. Although excellent long-term results have been described for the classic two-patch te