Roman Sekelyk, Maksym Delikatnyi, Dmytro Kozhokar, Ibrahim Yusifli, Danylo Shypov, Andrii Kurkevych, Illya Yemets
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引用次数: 0
摘要
右锁骨下动脉(AORSA)起源于右肺动脉异常是一种罕见的先天性畸形,通常通过计算机断层扫描、磁共振成像或血管造影术确诊。我们介绍了一个非常罕见的病例,该病例在新生儿出生后数小时内诊断出 AORSA,并通过手术矫正了同时存在的大动脉 d 型横位。由于当地医院和患者条件十分危急,无法进行额外的横断面成像检查。通过临床症状怀疑诊断,经胸超声心动图确诊,患者被紧急送入手术室。我们讨论了这名患有大动脉d横位和右肺动脉AORSA的患儿的临床和超声心动图征象。
Anomalous Origin of the Right Subclavian Artery from the Right Pulmonary Artery in a Patient with d-Transposition of the Great Arteries: Diagnosis and Surgical Treatment.
Anomalous origin of the right subclavian artery (AORSA) from the right pulmonary artery is a rare congenital anomaly usually diagnosed by computed tomography, magnetic resonance imaging, or angiography. We present a very rare case of diagnosis and surgical correction of AORSA coexisting with d-transposition of the great arteries in a newborn's first hours of life. Due to the critical local hospital and patient conditions, additional cross-sectional imaging was not feasible. The diagnosis was suspected by clinical signs, confirmed by transthoracic echocardiogram, and the patient was urgently taken to the operating room. We discuss clinical and echocardiographic signs of this child with d-transposition of the great arteries and AORSA from the right pulmonary artery.