Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Hiroshi, Ishitoya"'
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-4 (2020)
Abstract Background Coronary involvement is rare but can be critical in patients with aortitis. Although cardiac ischemia can be resolved by coronary artery bypass grafting (CABG), patients complicated with cardiac ischemia, calcified aorta, and valv
Externí odkaz:
https://doaj.org/article/3d85771196c34e0a9c4acdc3cb9f4cf8
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-3 (2020)
Abstract Background Retroaortic innominate vein is a rare anomaly. It has been reported in patients with congenital anomalies such as Tetralogy of Fallot or right aortic arch. However, isolated retroaortic innominate vein is quite rare. Case presenta
Externí odkaz:
https://doaj.org/article/05cadde5d13b40fab7812d39930d1779
Autor:
Taisuke Nakayama, Mayuko Nakayama, Takashi Harada, Shingo Isshiki, Hideki Sasaki, Hiroshi Ishitoya
Publikováno v:
SAGE Open Medical Case Reports, Vol 7 (2019)
Neurofibromatosis type 1, also called von Recklinghausen’s disease, is a hereditary congenital disorder that affects tissues of neuroectodermal or mesodermal origin. This disease has various manifestations, including pigmented skin lesions, cutaneo
Externí odkaz:
https://doaj.org/article/6f075408426b49089d0bc5fd7bc0e7d2
Autor:
Makana, Inari, Kazuma, Maisawa, Akiko, Yamagata, Takashi, Harada, Ken, Takahashi, Ichiro, Yoshioka, Hiroshi, Ishitoya
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 75(11)
A 73-year-old man after total arch replacement with open stent graft (OSG) technique for Stanford type B aortic dissection was found to have expanding descending aortic aneurysm. Contrast-enhanced computed tomography (CT) showed distal stent graft-in
Publikováno v:
Japanese Journal of Cardiovascular Surgery. 49:58-61
Publikováno v:
Cureus.
Publikováno v:
Journal of Cardiac Surgery. 35:2382-2384
A 72-year-old man was referred to our institution because of an arch aneurysm and acute aortic dissection (thrombosed Stanford type A). Anti-impulse therapy was initiated. He developed a high fever after admission. Blood culture was negative. Five da
Publikováno v:
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-3 (2020)
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-3 (2020)
Background Retroaortic innominate vein is a rare anomaly. It has been reported in patients with congenital anomalies such as Tetralogy of Fallot or right aortic arch. However, isolated retroaortic innominate vein is quite rare. Case presentation A 63
Publikováno v:
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-4 (2020)
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-4 (2020)
Background Coronary involvement is rare but can be critical in patients with aortitis. Although cardiac ischemia can be resolved by coronary artery bypass grafting (CABG), patients complicated with cardiac ischemia, calcified aorta, and valve insuffi
Publikováno v:
Interactive cardiovascular and thoracic surgery. 31(2)
The surgical management for type A acute aortic dissection complicated with carotid artery occlusion remains controversial. Between December 2012 and June 2017, 127 patients who presented with type A acute aortic dissection were operated on in our ho