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A Case of Right Sided Aortic Arch Combined with Atrial Septal Defect
하근진,성명준,이영수,이진배,류재근,이섭,최지용,권오천,장성국,김기식 한국심초음파학회 2011 Journal of Cardiovascular Imaging (J Cardiovasc Im Vol.19 No.1
Right sided aortic arch is an uncommon congenital anomaly. It can be classified into three types, depending on the left aortic arch’s degenerating pattern and the branching pattern of the great vessels. It can be associated with major congenital heart disease, depending on the type of right sided aortic arch. We report a case of an 18-years-old female who has right sided aortic arch with atrial septal defect (ASD). In our case, the patient had a right sided aortic arch and aberrant left subclavian artery, also she had ASD (ostium secundum) and moderate tricuspid regurgitation with pulmonary hypertension. The patient was successfully performed patch closure of ASD and tricuspid valve annuloplasty via midline sternotomy. The patient had uneventful postoperative course.
김정현,하근진,성명준,정진욱,김소연,문성희,이영수 대한심장학회 2011 Korean Circulation Journal Vol.41 No.10
Coronary artery anomalies are diagnosed in 0.6 to 1.5% of patients who undergo coronary angiography (CAG). They may present with life threatening conditions but are generally asymptomatic. Recognition and adequate visualization of the anomaly is essential for correct management of the condition. However, in some cases the exact orifice and course of an anomalous coronary vessel cannot be selectively identified by CAG. In this report, a 54-year-old man was admitted to the hospital with acute inferior myocardial infarction and had an anomalous origin of the left circumflex coronary artery (LCX) from the first diagonal branch (D1). In CAG, the right CAG showed no significant stenosis and fortunately we found an anomalous origin of the LCX from the D1. The course of LCX was precisely established by 64-slice multi-detector computed tomography.
배경륜,이영수,김병규,하근진,김소연,최지용,김기식 대한심장학회 2010 Korean Circulation Journal Vol.40 No.1
Coronary embolism is an uncommon cause of myocardial infarction. A 48-year-old male presented with typical chest pain of an MI. There was no definite ST segment change on electrocardiogram (ECG) and no elevation of myocardial enzymes. Coronary angiography (CAG) revealed occlusion of the distal left anterior descending coronary artery (dLAD), the distal left circumflex coronary artery (dLCX), the diagonal branch (D) and the obtuse marginal branch (OM), with a large filling defect in the left main coronary artery (LMA) that caused the myocardial infarction. We considered the possibility that coronary embolization was caused by the migration of a thrombus in the LMA during CAG. We did balloon angioplasty in the dLAD, dLCX, OM and D and treated the patient with glycoprotein IIb/IIIa receptor antagonist. However, thrombi remained in the dLAD, OM, and dLCX. After 3 days of anti-thrombotic treatment, follow-up CAG revealed only slight resolution of thrombi in the LAD. After triple antiplatelet agent medication for 1 year, a follow-up CAG showed a resolution of the thrombi in all coronary arteries.
이승준,김지연,박정규,김성우,김지헌,김태원,하근진,손호상,정의달,원규장 영남대학교 의과대학 2010 Yeungnam University Journal of Medicine Vol.27 No.2
Primary thyroidlymphomaisarelatively rarethyroidtumorandusually anon-Hodgkin type.Its mostcommon histologic typeis the diffuselarge B celllymphoma followed by mucosa-associated lymphoid tissue(MALT).Itisknown to befrequently associated with autoimmune thyroiditis such as Hashimoto's thyroiditis.We reportthree cases ofthyroid lymphomaatasingleinstitutionwithareview oftheliterature.