Although anomalous LBCV courses are very rare before delivery, they have been reported given the widespread use of fetal echocardiography [4,5,6,7,8,9]. The 3VT view is the most important view for the diagnosis of anomalous LBCV courses because the 3VT view can show fetal blood vessels, cardiac vessels, and the thymus [3, 10, 11]. Normally, the 3VT view is slightly deflected to the head of the fetus, and the LBCV can be displayed above the aortic arch and behind the thymus [5]. In previous studies, fetal retroesophageal LBCV had been reported [4, 7, 8]. Very few studies have also used STIC technology to describe retroesophageal LBCV in fetuses7. Prenatal diagnosis of subaortic LBCV and intrathymic LBCV were rarely reported, mainly in children or adults with CT and magnetic resonance imaging (MRI) findings [1, 12]. This study shows that the HD-flow combined with STIC can help show the adjacent relationship between the LBCV and aortic arch, and it has high clinical application value for accurately diagnosing the anomalous LBCV courses in fetuses.
The retroesophageal LBCV in the 3VT view can show that the transverse LBCV runs behind the aorta and trachea and then enters the RSVC through the azygous vein. Retroesophageal LBCV can form a “U”-shaped structure with the aortic arch. However, the color Doppler ultrasound image shows that the “U”-shaped structure has a different color, which needs to be distinguished from the right aortic arch (RAA). The RAA shows a U-shaped vascular ring of the same color. In addition, spectral Doppler ultrasonography can be used to observe the low-velocity venous blood flow spectrum instead of the arterial spectrum with retroesophageal LBCV. This study shows that HD-flow combined with STIC technology can intuitively display the retroesophageal LBCV finally flowing into the RSVC through the azygous vein.
When the LBCV runs inside the thymus, the LBCV is in a more forward position, partly curved, and merges into the RSVC from left to right. Ultrasound images showed an increase in the distance between the LBCV and the left brachiocephalic artery (LBCA) in the 3VT view. It is defined by the presence of thymic tissues between the LBCV and LBCA. A few studies have reported about the fetal intrathymic LBCV. Some studies have shown that the intrathymic LBCV may be more common in neonates. The main reason is that most intrathymic LBCV cases are isolated and easily missed. This study shows that the use of HD-flow combined with STIC can display the relationship between the LBCV and the thymus, and it can assist in diagnosing intrathymic LBCV in fetuses. When thymic surgery is required after birth, injuries to the LBCV and adverse outcomes should be monitored.
Subaortic LBCV is also known as LBCV in a low position. In this case, the LBCV runs under the aortic arch and enters the RSVC. This type is also rarely reported before delivery. Subaortic LBCV is often associated with conus trunk and aortic arch malformation. With the gradual application of imaging techniques such as CTA and MRI in clinical examinations, the subaortic LBCV is more commonly found in children and adults. Because the subaortic LBCV is often missed, its incidence may be underestimated. In our study, only three cases of isolated subaortic LBCV were identified, which was lower than the cases with cardiac malformations. The most common cardiac malformations of subaortic LBCV are RAA with aberrant left subclavian artery (ALSA) and cervical aortic arch (CAA). The RAA with ALSA and CAA can closely related to 22q11.2 chromosome microdeletion. Therefore, in fetuses having an RAA with ALSA or CAA, subaortic LBCV should be excluded and chromosomal copy number variants should be detected. In addition, subaortic LBCV, right pulmonary artery, and trachea can be displayed under the aortic arch in the long-axis view of the aortic arch, which is important to determine subaortic LBCV, but it is not easy to show in every case.
After anomalous LBCV courses are confirmed prenatally, comprehensive prenatal ultrasonography and fetal echocardiography are necessary to detect fetal abnormalities in extracardiac or intracardiac structures. If necessary, chromosome analysis is required. A study reported that anomalous LBCV courses are not clearly related to chromosomal abnormalities [13]. Most cases of isolated anomalous LBCV courses are not associated with the presence of other malformations, and in these cases, chromosomal alterations are not usually present [3]. Isolated anomalous LBCV courses have a better clinical prognosis because of less compression of the trachea or esophagus, which can be considered as a normal variant. In a fetus with an anomalous LBCV course, the cardiologist should be reminded about this anomaly because it may affect the centerline or heart surgery method [14]. HD-flow render mode and STIC can more clearly and intuitively display the adjacent relationship between the aortic arch and the LBCV, and it can better display the entire drainage route of the LBCV than 2D image. With this method, we cannot only explain the anatomical variation of the anomalous LBCV course to the pregnant woman, but also mention that it has certain guiding significance for making decisions about cardiac malformation surgery and potential cardiac interventional surgery in the future. In this study, although most fetuses with anomalous LBCV courses can be diagnosed by 3VT view combined with color blood flow before childbirth, HD-flow combined with STIC can dynamically better display the anomalous LBCV course and make a clear classification than 2D image. In addition, the STIC image of anomalous LBCV courses is highly consistent with the postpartum ultrasound images or CTA. HD-flow combined with STIC presents an intuitive 3D structure of the anomalous LBCV courses, which is helpful for the accurate diagnosis of the anomalous LBCV course before delivery.
Obtaining 3D images of the anomalous LBCV course in fetuses may be affected by factors such as fetal movement. Therefore, images may be obtained while the fetus is in a quiet state. In addition, sufficient patience is necessary to obtain a satisfactory STIC image of the anomalous LBCV course in fetuses. Finally, due to the small sample size in this study, a larger-scale prospective evaluation and analysis should be carried out in the future to obtain more objective indicators and information to guide clinical practice.