首页> 外文期刊>Pediatric cardiology >Prenatal Ultrasonic Diagnosis and Prognostic Analysis of Isolated Left Subclavian Artery (ILSCA) and Left Brachiocephalic Trunk (ILBCT) Malformation
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Prenatal Ultrasonic Diagnosis and Prognostic Analysis of Isolated Left Subclavian Artery (ILSCA) and Left Brachiocephalic Trunk (ILBCT) Malformation

机译:孤立左侧亚克拉夫动脉(ILSCA)和左心血管躯干(ILBCT)畸形的产前超声诊断及预后分析

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The purpose of the study was to explore the prognosis, as well as antenatal ultrasonic features of isolated left subclavian artery (ILSCA) and isolated left brachiocephalic trunk (ILBCT) malformations, in order to improve prognosis and provide guidance for prenatal diagnosis. The origin and routing of cephalic and cervical vessels were observed in patients diagnosed with right aortic arch or right arterial duct arch in our hospital from March 2015 to March 2017, and the spectrum features related to ILSCA and ILBCT were analyzed. Fetuses diagnosed as ILSCA, or, and ILBCT were followed up for 3?months after birth. At the same time, a literature review was carried out for ILBCT and ILSCA in Pubmed. In our study, two cases with ILSCA and ILBCT were both diagnosed prenatally. They are not accompanied by other congenital malformations or chromosome abnormalities. No abnormality was found during postnatal follow-up except that left radial pulsation was weakened and blood pressure of the left upper limb decreased in baby with ILSCA. In baby with ILBCT, in addition to these abnormal changes, the left common carotid artery pulse disappearance too. In pubmed, three of 12 ILSCA or ILBCT did not have other congenital malformation or chromosome abnormalities. They were not diagnosed until the age of 3, 10, and 47 because of school exams or atypical symptoms, such as headaches, chest pain. Symptom of ILBCT or ILSCA without other abnormality is silent, and therefore they cannot be diagnosed timely after birth prenatal diagnosis is necessary for they can be treated in time.
机译:该研究的目的是探讨分离的左亚克拉夫动脉(ILSCA)的预后,以及分离的左右脑膜躯干(ILBCT)畸形的产前超声特征,以改善预后并为产前诊断提供指导。从2015年3月到2017年3月诊断患有右侧主动脉弓或右动脉管拱门的患者的患者中观察到头孢菌和宫颈血管的起源和路由,分析了与ILSCA和ILBCT相关的频谱特征。诊断为ILSCA的胎儿,出生后3个月,随访3个月。与此同时,在PubMed中对ILBCT和ILSCA进行了文献综述。在我们的研究中,两种患有ILSCA和ILBCT的病例均在预先诊断出来。它们不伴随着其他先天性畸形或染色体异常。在出生后随访期间没有发现异常,除了左径向脉动被削弱,左上肢的血压在婴儿用ILSCA减少。在婴儿用ILBCT,除了这些异常变化外,左侧颈动脉脉冲脉冲消失。在pubmed中,12种Ilsca或Ilbct中的三种没有其他先天性畸形或染色体异常。由于学校考试或非典型症状,它们未被诊断为3,10和47岁,例如头痛,胸痛。 ILBCT或ILSCA的症状没有其他异常的沉默是沉默的,因此它们不能在出生后诊断后及时诊断,它们可以及时处理。

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