A 53-year-old male presented with chest wall pain. He underwent chest CT scan with 5-mm section thicknesses using a multidetector CT scanner (Aquilion 64, Toshiba Medical Systems, Tokyo, Japan). The images were acquired within a single breath hold after injection of the contrast medium (Iobrix 350; injection rate, 2.2 mL/sec; volume, 100 mL).

The CT scan revealed lung cancer in the right upper lobe. Incidentally, the CT identified an ALBCV that was divided into two branches at the level of the aortic arch (Fig. 1). The anterior branch was above the aortic arch and coursed anterior to the left common carotid artery and brachiocephalic artery, before draining into the superior vena cava (SVC). The posterior branch was below the aortic arch and coursed posterior to the ascending aorta. Both branches drained into the SVC separately and no other cardiovascular anomaly was noted. The patient refused further evaluation and operation.

The brachiocephalic veins are two large vessels at the junction of the neck and thorax, which result from union of the internal jugular and subclavian veins in the superior mediastinum. The LBCV begins behind the sternal end of the clavicle and ends at upper half of the manubrium sterni, and ultimately uniting with the right brachiocephalic vein to form the SVC. The LBCV usually courses obliquely downward and to the right, passing superior and anterior to the aortic arch and anterior to the left subclavian, left common carotid, and brachiocephalic arteries (1). Rarely, this vein follows an anomalous course. Kerschner described the first case of an anomalous brachiocephalic vein beneath the aortic arch more than 100 years ago (2). Takata reported eight cases of LBCV in an anomalous position in 1992. Six cases were single aberrant LBCV, and two cases were double brachiocephalic veins (3).

In the embryonic stage (approx. 4 weeks), the primordium of the systemic veins appears as paired precardinal and postcardinal veins that unite on each side to form the common cardinal vein which opens into the primitive sinus venosus. At 8 weeks, between the right and left precardinal veins, a new transverse anatomic channel (i.e. the upper transverse capillary plexus), develops and forms the LBCV. The portion above the anastomosis and the LBCV of the right precardinal vein become the right brachiocephalic vein. The distal portion of the right precardinal vein and the right common cardinal vein become the SVC. Subsequently, the subcardinal vein atrophies are replaced by the supracardinal vein. At term, the right azygos represents the site of the right postcardinal vein, and the azygos vein orifice marks the junction of the precardinal vein and common cardinal venous components of the SVC (4567). The exact cause of ALBCV is unknown. Normal precardinal anastomosis develops ventrally to the arterial structures. But, ALBCV is thought to result from the precardinal anastomosis being situated posterior to the truncus arteriosus, and the double LBCV is the consequence of both ventral and dorsal precardinal anastomosis (8).

Takada et al. (3) reported four major patterns of ALBCV. The report only described various types of single brachiocephalic veins: a, ALBCV crossing the midline above aortic arch and behind its major cephalic branch; b, ALBCV crossing the midline beneath the aortic arch, above the pulmonary artery, and in front of the patent ductal arteriosus; a+b, hybrid patterns of a and b, c, ALBCV crossing the midline beneath the aortic arch, above the pulmonary artery, and behind the patent ductal arteriosus; d, ALBCV crossing the midline below the pulmonary arterial trunk. However, there are only a few reports of double LBCV (39). Yigit et al. (9) reported a case of double ALBCV. In this anomaly, the anterior branch was above the aortic arch and behind the truncus brachiocephalicus, and finally drained into the superior vena cava. The posterior branch coursed posterior to the trachea and esophagus, and joined with the azygos vein before draining into the SVC. Takada et al. (3) reported cases of double ALBCVs, in which the posterior branch courses inferior to the aortic arch, behind the ascending arch and anterior to the trachea, and finally draining into the SVC without joining with the azygos vein. We believe that the circumaortic type is different from the case reported by Yigit et al. (i.e. retrotracheal).

ALBCV causes no subjective symptoms and the diagnosis is incidental in most cases. Although an ALBCV by itself seems to be of no functional importance, we assessed its importance in terms of associated conditions and its possible relevance to subsequent operations.

The most frequent cardiac defects associated with ALBCV were tetralogy of Fallot and a ventricular septal defect with pulmonary atresia (10). This anomaly is also important when performing central venous catheters or cardiac surgeries. This may cause difficulties in introducing left-sided central lines unless they know the anatomy. Surgeons may not identify the anomalous course if they are not informed beforehand, which can significantly alter their surgical approach.

Moreover, recognition of this aberrant variation of the LBCV is of clinical importance to the radiologist, since a retro-aortic or subaortic segment of the ALBCV may mimic an enlarged lymph node and could be misinterpreted as an enlarged lymph node on non-contrast CT scans (9) (Fig. 2). Contrast-enhanced CT scans help in distinguishing aberrant vessels and lymph nodes. In this report, we describe the radiologic findings of a circumaortic ALBCV. It is important for radiologists to be familiar with the CT appearance of these ALBCVs.