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首页> 外文期刊>American Journal of Perinatology Reports >Fetal Heterotaxy with Tricuspid Atresia, Pulmonary Atresia, and Isomerism of the Right Atrial Appendages at 22 Weeks
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Fetal Heterotaxy with Tricuspid Atresia, Pulmonary Atresia, and Isomerism of the Right Atrial Appendages at 22 Weeks

机译:胎儿异位症与三尖瓣闭锁,肺闭锁和右心耳附件在第22周的异构现象。

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摘要

We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex cardiac abnormality, ventriculoarterial discordance, juxtaposition of the aorta and the inferior vena cava to the right side, pulmonary atresia, and anomalous pulmonary venous return to the morphological right atrium. Tricuspid atresia, which is an extremely rare lesion within heterotaxy spectrum disorders, was present. Postnatal investigations confirmed all prenatally diagnosed abnormalities, with additional findings of pulmonary atresia with discontinuous pulmonary arteries and bilateral arterial ducts, asplenia, and bilateral eparterial bronchi. To our knowledge, tricuspid atresia in the setting of isomerism of the right atrial appendages has not previously been diagnosed or reported prenatally. Because of the complexity of cardiac lesions that may be present in cases of atrial isomerism, these disorders should be considered even if sonographic findings are uncommon or atypical.
机译:我们报告与三尖瓣闭锁相关的右心房异构妊娠22周时的准确的产前诊断。该胎儿存在右房耳异构现象的几个独特的超声特征:复杂的心脏异常,心室动脉不协调,主动脉与右侧下腔静脉的并置,肺动脉闭锁和肺静脉异常返回形态右中庭。存在三尖瓣闭锁,这是异源性光谱疾病中极为罕见的病变。产后调查证实了所有产前诊断的异常,另外发现肺动脉闭锁伴不连续的肺动脉和双侧动脉导管,无力和双侧心支气管。据我们所知,产前未诊断或报道右房附肢异构性情况下的三尖瓣闭锁。由于在心房异构症中可能存在心脏病变的复杂性,因此即使超声检查结果不常见或不典型,也应考虑这些疾病。

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