Acherman Ruben J, Evans William N, Galindo Alvaro, Collazos Juan C, Rothman Abraham, Mayman Gary A, Luna Carlos F, Rollins Robert, Kip Katrinka T, Berthody Dean P, Restrepo Humberto
Fetal Cardiology Program, Children's Heart Center, Las Vegas, NV 89109, USA.
J Ultrasound Med. 2007 Aug;26(8):1077-82. doi: 10.7863/jum.2007.26.8.1077.
The purpose of this series was to assess the incidence, anatomic variants, and implications of an absent ductus venosus (ADV) in patients referred for fetal echocardiography.
We searched our fetal cardiology database for diagnoses of ADV from May 2003 to December 2006.
During the study period, we performed 1328 fetal echocardiographic examinations in 990 fetuses. We found 6 cases of ADV (6/1000). Indications for fetal echocardiography were cardiomegaly, dilated umbilical or systemic veins, and extracardiac abnormalities. We identified 5 anatomic variants of ADV. In 2 patients, the umbilical vein connected to the systemic venous circulation by way of the portal sinus: via an abnormal venous channel from the portal sinus to the right atrium (case 1) and presumably via hepatic sinusoids to the hepatic veins (case 2). In the remaining 4 patients, the umbilical vein bypassed the portal sinus and the liver and connected to the systemic venous circulation via an abnormal venous channel: from the umbilical vein to the right atrium (case 3), from the umbilical vein to the inferior vena cava (cases 4 and 5), and from the umbilical vein to the right iliac vein (case 6). All patients survived; 2 required cardiovascular intervention. No intervention was required in 3 patients.
An ADV should be ruled out in a fetus with unexplained cardiomegaly or dilatation of the umbilical vein, systemic veins, or portal sinus. To our knowledge, prenatal diagnosis of an ADV with an abnormal communication between the portal sinus and the right atrium has not been reported previously. The portosystemic communication persisted after birth and required device occlusion.
本系列研究旨在评估接受胎儿超声心动图检查的患者中静脉导管缺如(ADV)的发生率、解剖变异及其影响。
我们在胎儿心脏病数据库中搜索2003年5月至2006年12月期间ADV的诊断情况。
在研究期间,我们对990例胎儿进行了1328次胎儿超声心动图检查。我们发现6例ADV(6/1000)。胎儿超声心动图检查的指征为心脏扩大、脐静脉或体静脉扩张以及心外异常。我们确定了ADV的5种解剖变异。在2例患者中,脐静脉通过门静脉窦与体静脉循环相连:通过从门静脉窦到右心房的异常静脉通道(病例1),可能通过肝血窦到肝静脉(病例2)。在其余4例患者中,脐静脉绕过门静脉窦和肝脏,通过异常静脉通道与体静脉循环相连:从脐静脉到右心房(病例3),从脐静脉到下腔静脉(病例4和5),以及从脐静脉到右髂静脉(病例6)。所有患者均存活;2例需要心血管介入治疗。3例患者无需干预。
对于原因不明的心脏扩大或脐静脉、体静脉或门静脉窦扩张的胎儿,应排除ADV。据我们所知,以前尚未报道过门静脉窦与右心房之间存在异常交通的ADV的产前诊断。出生后门体分流持续存在,需要使用装置封堵。