scholarly journals A rare case of concomitant aortic regurgitation and coronary ostial stenosis due to cardiovascular syphilis

2021 ◽  
Vol 5 (3) ◽  
Author(s):  
Daichi Fujimoto ◽  
Takayoshi Toba ◽  
Kenji Okada ◽  
Ken-Ichi Hirata
1998 ◽  
Vol 37 (1) ◽  
pp. 56-59 ◽  
Author(s):  
Hiroki AIZAWA ◽  
Akira HASEGAWA ◽  
Masashi ARAI ◽  
Fumio NAGANUMA ◽  
Masako HATORI ◽  
...  

2017 ◽  
Vol 46 (5) ◽  
pp. 255-259
Author(s):  
Mari Sakai ◽  
Saori Nagura ◽  
Masaya Aoki ◽  
Shigeki Yokoyama ◽  
Katsunori Takeuchi ◽  
...  

2012 ◽  
Vol 6 (6) ◽  
pp. e173-e175 ◽  
Author(s):  
Katsuhiko Matsuyama ◽  
Masahiko Kuinose ◽  
Yasunari Iida ◽  
Toru Iwahashi ◽  
Katsutoshi Sato ◽  
...  

1995 ◽  
Vol 24 (3) ◽  
pp. 175-177 ◽  
Author(s):  
Yasushi Sato ◽  
Susumu Ishikawa ◽  
Akio Ohtaki ◽  
Kazuhiro Sakata ◽  
Yoshimi Otani ◽  
...  

2017 ◽  
Vol 34 (1) ◽  
pp. 81-84
Author(s):  
Mohit Sharma ◽  
Sunil Dixit ◽  
Anil Sharma ◽  
Parth Vaghela ◽  
Jai Kishan Suthar

2014 ◽  
Vol 8 (1) ◽  
pp. 23-25 ◽  
Author(s):  
Pankaj Garg ◽  
Hazlyna Kamaruddin ◽  
Rachel Orme ◽  
Victoria Watt

Congenital quadricuspid aortic valve (QAV) is a rare cardiac anomaly. Several different anatomical variations of a quadricuspid aortic valve have been described. Aortic regurgitation is the predominant valvular dysfunction associated with QAV and patients tend to present in their 5th or 6th decade of life. This anomaly is rarely picked up by transthoracic echocardiogram (TTE). A comprehensive transoesophageal echocardiography (TOE) study is more likely to diagnose it. We describe a very rare type of QAV – Type F in a 52-year-old lady who presented with symptoms of shortness of breath and pre-syncope. We include TOE images and intra-operative valve images.


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