A report study of successful surgical treatment of an aorto-left ventricular tunnel in a 5-year-old boy: differential diagnosis from other congenital heart diseases with similar clinical symptoms.

Alireza Yaghoubi Golverdi, Amirhossein Jalali, Mohammad Mahdavi, Seyed Salaheddin Nabavi, Mahmoud Ganjifard, Maryam Bahramian, Mozhgan Bahramian, Seyed Shervin Shafiei
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Abstract

Background: Aorto-left ventricular tunnel (ALVT) is a rare congenital anomaly. In this condition, the aorto-ventricular tunnel is a congenital extracardiac channel that connects the ascending aorta to the left ventricle above the sinotubular junction.

Case presentation: A 5-year-old boy presented with fatigue during physical activity, leading to visiting a pediatric specialist. Upon examination, a continuous murmur, predominantly diastolic, was detected. Suspecting aortic insufficiency, the patient was referred for further evaluation. Transthoracic echocardiography revealed a congenital ALVT.

Conclusion: Although congenital ALVT is a rare congenital heart disease, its clinical symptoms may overlap with other congenital heart diseases, such as tetralogy of Fallot without pulmonary stenosis and patent ductus arteriosus. Differential diagnosis, such as the absence of a wide pulse pressure, can be helpful in distinguishing between these conditions.

一例5岁男童成功手术治疗主动脉-左心室隧道:与其他具有相似临床症状的先天性心脏病的鉴别诊断
背景:主动脉-左心室隧道(ALVT)是一种罕见的先天性异常。在这种情况下,主动脉-心室隧道是一条先天性的心外通道,连接升主动脉和左心室,位于窦小管交界处上方。病例介绍:一名5岁男孩在体育活动中出现疲劳,导致去儿科专家就诊。经检查,发现持续的杂音,以舒张期为主。怀疑主动脉功能不全,患者转介进一步评估。经胸超声心动图显示先天性ALVT。结论:先天性ALVT虽然是一种罕见的先天性心脏病,但其临床症状可能与其他先天性心脏病重叠,如无肺狭窄的法洛四联症、动脉导管未闭等。鉴别诊断,如没有宽脉压,可以帮助区分这些情况。
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