Occlusion of the Right Coronary, Artery as Sequelae of Kawasaki Disease: The Clinical Features of 9 Cases

Cardiology ◽  
1995 ◽  
Vol 86 (3) ◽  
pp. 207-210
Author(s):  
Noboru Takahashi ◽  
Junichiro Fukushige ◽  
Takayuki Hijii ◽  
Hisaji Igarashi ◽  
Akio Ooshima ◽  
...  
2017 ◽  
Vol 8 (5) ◽  
pp. 600-604 ◽  
Author(s):  
Samuel E. Ramírez-Marroquín ◽  
Alejandra Iturriaga-Hernández ◽  
Juan Calderón-Colmenero ◽  
Antonio Benita-Bordes ◽  
Jorge L. Cervantes-Salazar

Background: The indications for pediatric coronary revascularization are diverse. There are a large proportion of patients with sequelae of severe inflammatory diseases such as Kawasaki disease, and other less common causes. Methods: Retrospective review of ten pediatric patients undergoing coronary artery bypass surgery from January 2004 to December 2016. Results: Ten children and adolescents ranging in age from 2 to 17 (median, 6) years at operation were followed up for as long as 13 years with a median follow-up of 2 years. The surgical indications include ischemia symptoms and/or coronary stenosis angiographically documented. Diagnoses include Kawasaki disease, anomalous origin of the left coronary artery from the pulmonary artery, and iatrogenic lesion of the right coronary artery. All the surgical procedures were performed with cardiopulmonary bypass with crystalloid cardioplegic arrest. The number of distal anastomoses was 1.6 per patient, and the left internal thoracic artery was used in one patient, the right internal thoracic artery in four patients, bilateral internal thoracic artery in four patients, and bilateral internal thoracic artery plus left radial artery in one patient, most frequently for right coronary artery revascularization. The patients underwent noninvasive diagnostic study during follow-up to evaluate their coronary status. The ten patients had no symptoms, and there was no mortality. Conclusions: Although survival was excellent after pediatric coronary bypass in our center, we need to continue the follow-up. Coronary revascularization by means of arterial grafting is a safe and reliable surgical modality for coronary disease in children.


2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Alejandra Peña-Juárez ◽  
Miguel Angel Medina-Andrade ◽  
Itzel Estefani Ríos Olivares ◽  
José Luis Colín-Ortíz ◽  
Marco Antonio Yamazaki-Nakashimada ◽  
...  

2010 ◽  
Vol 10 (2) ◽  
pp. 317-318 ◽  
Author(s):  
Madhankumar Kuppuswamy ◽  
Philemon Gukop ◽  
George Sutherland ◽  
Chandrasekaran Venkatachalam

1979 ◽  
Vol 43 (6) ◽  
pp. 1103-1108 ◽  
Author(s):  
Michele A. Codini ◽  
Philip W. Hassan ◽  
Robert G. Hauser ◽  
Marshall D. Goldin ◽  
Joseph V. Messer

2019 ◽  
Vol 25 (2) ◽  
pp. 137
Author(s):  
E. V. Rosseĭkin ◽  
V. V. Bazylev ◽  
E. E. Kobzev ◽  
A. B. Voevodin ◽  
P. A. Batrakov ◽  
...  

2007 ◽  
Vol 10 (4) ◽  
pp. E325-E328 ◽  
Author(s):  
Ali Gürbüz ◽  
Ufuk Yetkin ◽  
Ömer Tetik ◽  
Mert Kestelli ◽  
Murat Yesil

2015 ◽  
Vol 18 (6) ◽  
pp. 253
Author(s):  
Renyuan Li ◽  
Yiming Ni ◽  
Peng Teng ◽  
Weidong Li

<p>Coronary artery fistula (CAF) is a rare entity. Sometimes it may associate with mild diffuse or segmental coronary ectasia. CAF with giant coronary artery is exceptionally rare. We present a unique case of a 49-year-old female patient with a giant right coronary artery of diffuse ectasia coexisting with a fistula draining into the right ventricle. To our best knowledge, CAF with diffuse coronary ectasia of such giant size has never been reported. The patient was treated successfully by resection of the dilated right coronary artery, fistula closure, and coronary artery bypass grafting.</p>


2014 ◽  
Vol 17 (4) ◽  
pp. 196
Author(s):  
Erhan Kaya ◽  
Halit Yerebakan ◽  
Daniel Spielman ◽  
Omer Isik ◽  
Cevat Yakut

Occlusion of a coronary artery by an acute type A aortic dissection presents a life-threatening emergency that is rarely seen and easy to misdiagnose. We present the case of a 75-year-old male who experienced sudden onset of severe left-sided chest pain due to an acute type A aortic dissection that obstructed the right coronary artery. Following an initial misdiagnosis of acute coronary syndrome, imaging revealed the presence of an aortic dissection. An emergency modified Bentall procedure was performed, in which the damaged aorta and aortic valve were replaced.


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