“…Many authors include some embryological aspects of the BCT in their descriptions, some discrepancies appearing among those who state that the BCT and the subclavian artery originate from the 4 th aortic arch (Savastano et al, 2002;Smith Agreda et al, 1992;Williams and Warwick, 1992) and others who associate their origin with the aortic sac (Moore, 1982;Sadler and Langman, 2005). Embryological features determine anatomical variations and anomalies that often occur in the BCT : 1) at its origin, such as a common origin with the left common carotid artery (Chahwan et al, 2006;Jakanani and Adair, 2010;Katz et al, 2006;Moskowitz and Topaz, 2003;Turgut et al, 2001), coming from any of the pulmonary arteries (Gil-Jaurena et al, 2011;Martin et al, 2006) or absence (Chaoui et al, 2005;McDowell et al, 1980;Natsis et al, 2011), 2) in length and anatomical relations (Hori et al, 2004;Maldjian et al, 2007;Ozlugedik et al, 2005;Racic et al, 2005), 3) in its branching, such as the observed origination of a coronary artery (Davies and Lie, 1977;Duran et al, 2008), a pulmonary artery (Hung et al, 2001;Tsutsumi et al, 1991), a thyroidea ima artery (Yilmaz et al, 1993) and others. Most of the BCT-related publications are case reports, usually on anatomic anomalies with clinical consequences, or on diagnostic and surgical findings.…”