Chino M, Kawaguchi T, Sakai T, Okuno T
Department of Cardiology, Ashikaga Red Cross Hospital, Japan.
Angiology. 1991 Mar;42(3):256-60. doi: 10.1177/000331979104200311.
A patient who had high-output heart failure resulting from anastomosis of the intercostal and bronchial arteries to the right pulmonary artery is reported. The patient was a fifty-one year-old man who was admitted to our hospital with left heart failure. A radionuclide angiocardiogram revealed blood flow from the aorta to the right pulmonary artery. A descending aortogram revealed abnormally dilated right intercostal and bronchial arteries, which formed the anastomosis. The right pulmonary artery was visualized via that anastomosis. Tuberculous pleurisy in the patient's history was considered to be the cause of the anastomosis. The therapeutic procedure used was embolization via a catheter for the anastomosis, but most anastomoses could not be embolized. The present report is considered the first on anastomosis of the intercostal artery to the pulmonary artery to the extent that high-output heart failure occurs.
本文报道了一例因肋间动脉和支气管动脉与右肺动脉吻合导致高输出量心力衰竭的患者。该患者为一名51岁男性,因左心衰竭入院。放射性核素血管造影显示有血液从主动脉流向右肺动脉。降主动脉造影显示右肋间动脉和支气管动脉异常扩张,形成了吻合口。通过该吻合口可观察到右肺动脉。患者既往有结核性胸膜炎病史,被认为是吻合口形成的原因。所采用的治疗方法是通过导管对吻合口进行栓塞,但大多数吻合口无法栓塞。本报告被认为是关于肋间动脉与肺动脉吻合导致高输出量心力衰竭的首例报告。