nomalous origin of the right coronary artery (RCA) from the left coronary sinus is a rare congenital abnormality, with an estimated incidence of 0.3-1.3%, [1][2][3][4] in which the RCA consequently courses between the aorta and pulmonary trunk. Enlargement of the aorta and pulmonary trunk because of aging and exercise may compress the RCA, which causes myocardial ischemia, including acute myocardial infarction, angina pectoris and sudden death. [5][6][7][8][9][10] In cases manifesting as myocardial ischemia, surgical treatment is usually indicated. [8][9][10] We describe a 55-year-old woman with such an anomaly, in whom an unusual biventricular myocardial infarction occurred, closely associated with pulmonary thromboembolism (PTE).
Case ReportA 55-year-old Japanese woman with a 5-month history of precordial oppression and dyspnea was admitted to hospital in March 1993. The aortic artery blood pressure was 90/50 mmHg and the pulse rate was regular at 92 beats/min. Arterial blood gases with room air showed a partial pressure of oxygen of 61.2 mmHg, partial pressure of carbon dioxide 29.2 mmHg, and pH 7.456. Roentgenogram of the chest disclosed cardiac enlargement and a decreased vascular shadow in the right lower lung field. An electrocardiogram (ECG) showed ST-elevation in leads II,
Circulation Journal Vol.68, September 2004III, aVF, V3R and V4R, and T-wave inversion in the precordial leads (Fig 1). An echocardiogram depicted a markedly dilated right ventricle (RV), and displacement of the interventricular septum toward the left ventricle (LV) during systole. Emergency cardiac catheterization revealed that the RCA originated from the left coronary sinus, and that the proximal portion was compressed from the outside and the distal portion had collaterals from septal branches of the left anterior descending artery (Fig 2). Hemodynamic studies revealed elevation of the pulmonary artery pressure (55/34 mmHg), right pulmonary capillary wedge pressure (25 mmHg), and RV pressure at end-diastole (19 mmHg), which indicated pulmonary hypertension with a low cardiac index (1.97 L路min -1 路m -2 ). Pulmonary arteriography showed multiple intraluminal filling defects and dilatation of the proximal pulmonary arteries. The concentration of creatine kinase was elevated to 1,876 U/L with an MB band of 13%. The serum concentrations of aspartate aminotransferase (461 U/L) and lactic dehydrogenase (2,260 U/L) were also elevated. Acute deterioration of chronic PTE associated with myocardial infarction was strongly suspected. A perfusion lung scan showed multiple segmental defects, affecting the right lung more severely than the left (Fig 3A). Thallium-201 and technetium-99m-pyrophosphate dual isotope emission computed tomography depicted uptake of both isotopes (overlap) in the LV infero-posterior region, and significant technetium-99m-pyrophosphate accumulation was observed in the markedly thickened and dilated RV (Fig 4).Recent 3-dimensional imaging studies of the patient in October 2001 using computed tomographic and transesophage...