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최창휴,김삼현,박성식,류경민,김재현,서필원 대한흉부심장혈관외과학회 2000 Journal of Chest Surgery (J Chest Surg) Vol.33 No.5
Tracheo-innominate artery fistula is a rare, but it is one of the gravest complications next to tracheostromy. Early recognition and prompt surgical management is mandatory. The patient was a 66 year old women with MCA infarct who maintained tracheostomy for lyear. She had respiratory arrest due to the excessive bleeding through the tracheostomy site. We report an successful experience for control of bleeding by an innominate artery fistula division and primay suture closure under direct digital compression.
최창휴,박이태,박성식,류재욱,김재현,김삼현 대한흉부심장혈관외과학회 1999 Journal of Chest Surgery (J Chest Surg) Vol.32 No.3
심내막 심근섬유증은 비교적 드문 형태의 심근병증으로 섬유화와 혈전 등에 의해 심실충만의 제한과 심실강 유입부의 폐쇄를 가져온다. 병이 진행하면 심판막까지 침범해 방실판 역류를 일으킨다. 유일한 치료법은 심내막절제술과 판막대치술 등의 수술적 방법이다. 저자들은 수술적 치료를 시행했던 심내막 심근섬유증을 1례 치험하였다. 이에 관련된 문헌과 함께 보고하는 바이다. Endomyocardial fibrosis(EMF) is an unusual type of cardiomyopathy characterized by a restriction to the ventricular filling and an obliteration of the inflow portion in the ventricular cavity by a fibrosis and often by a thrombus formation. The atrioventricular valve may be involved, resulting in an atrioventricular valvular regurgitation. The only known effective treatments are endomyocardiectomy and replacement of regurgitant AV valves. We report the experience of a case of EMF which required surgical management.
최창휴,박철현,전양빈,이소영,이재익,박국양 대한흉부외과학회 2013 Journal of Chest Surgery (J Chest Surg) Vol.46 No.1
Background: Total arch replacement (TAR) is being more widely performed due to recent advances in operative techniques and cerebral protective strategies. In this study, the authors reviewed the relationship between TAR and early- and mid-term changes of the false lumen after TAR in acute type A aortic dissection. Materials and Methods: Twenty-six patients (aged, 54.7±13.3 years) who underwent TAR for acute type A dissection between June 2004 and February 2012 were reviewed. The relationship between the percentage change in the aortic diameter and the false lumen patency status was assessed by examining the early and late postoperative computed tomography imaging studies. Results: There were two in-hospital mortalities, one late death, and three follow-up loses. The mean follow-up duration for the final 21 patients studied was 54±19.0 months (range, 20 to 82 months). The incidence of false lumen thrombosis within 2 weeks of surgery in the proximal, middle, and distal thoracic aorta, and the suprarenal and infrarenal abdominal aorta were 67%, 38%, 38%, 48%, and 33%, respectively, and 57%, 67%, 52%, 33%, and 33% for those examined at a mean of 49±18 months after surgery, respectively. The false lumen regressed in 11 patients (42.3%). The aortic diameters were larger in the patients with a patent false lumen than those with a thrombosed false lumen at all levels of the descending aorta (p <0.05). Conclusion: TAR and a more complete primary tear-resection can be accomplished with a relatively low-risk of morbidity and mortality. Enlargement of the distal aorta significantly correlated with the false lumen patency status.
최창휴,김웅한,곽재건,김진현,정요천,김동진,오세진,이정렬,김용진,노준량 대한흉부외과학회 2004 Journal of Chest Surgery (J Chest Surg) Vol.37 No.11
Berry syndrome (interrupted aortic arch, aortopulmonary window, and aortic origin of right pulmonary artery with intact interventricular septum) is a very rare and complex cardiac malformation. We report a successful one-stage repair in a 14-day-old neonate without circulatory arrest. 대동맥궁단절과 우폐동맥이 대동맥에서 기시하는 형태의 대동맥폐동맥창의 조합인 Berry증후군은 매우 드문 복합심기형의 하나이다. 14일된 신생아에 있어서 국소순환하에 순환정지 없이 일차완전교정술을 시행하여 좋은 결과를 얻었기에 보고하는 바이다.