Literature DB >> 9453364

The formal pathogenesis of isolated common carotid or innominate arteries: the concept of malseptation of the aortic sac.

J Männer1, W Seidl, G Steding.   

Abstract

Deficient connections (= isolation) of the innominate artery or the common carotid artery to the aorta are rare congenital anomalies of the human aortic arch complex that are usually associated with a patent vascular connection between the isolated artery and a pulmonary artery. In the present study we demonstrate chick fetuses with a corresponding anomaly, the isolation of the brachiocephalic artery. In our chick fetuses the left brachiocephalic artery did not arise from the aortic arch, but was connected to the pulmonary trunk proximal (upstream) to the patent left and right ductus arteriosus. These cases are of interest because the presence of a congenital pulmonary-systemic arterial connection proximal (upstream) to the ductus arteriosus cannot be explained by the traditional concept of the morphogenesis of the aortic arch complex. The development of the normal and abnormal branching patterns of the aortic arch arteries is traditionally explained by transformation of the primitive embryonic pharyngeal arch arterial system due to obliteration of some of its vascular segments. Based on this concept, the isolation of an aortic arch artery can be explained by obliteration of vascular segments proximal and distal to this artery, whereas its connection to a pulmonary artery can be explained only by deficient obliteration (persistence) of the distal portion of the right or left sixth pharyngeal arch artery. The connecting "vascular segment" between an isolated aortic arch artery and the pulmonary circulation, therefore, is traditionally interpreted as a patent ductus arteriosus. The formal pathogenesis of congenital pulmonary-systemic arterial connections proximal (upstream) to the ductus arteriosus is discussed. The presented cases of isolation of the brachiocephalic artery are explained by disturbances in the partition of the embryonic aortic sac, possibly due to abnormal development of the "cardiac" neural crest.

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Year:  1997        PMID: 9453364     DOI: 10.1007/s004290050111

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  5 in total

1.  An isolated left common carotid artery from the main pulmonary artery: possible malseptation of the truncoaortic sac.

Authors:  N Kaushik; Z Saba; H Rosenfeld; H T Patel; K Martin; O Reinhartz; J J Lamberti
Journal:  Pediatr Cardiol       Date:  2005 Sep-Oct       Impact factor: 1.655

2.  Isolation of right internal carotid artery, persistent proatlantal 1 artery and rete mirabile in a child with 22q11 deletion syndrome.

Authors:  Flavio Requejo; Florencia Romina Strawich; Diana Mariela Mouratian; Timo Krings
Journal:  Childs Nerv Syst       Date:  2018-07-16       Impact factor: 1.475

3.  Isolated left brachiocephalic artery with the right aortic arch: A rare differential of large patent ductus arteriosus.

Authors:  Gajendra Dubey; Saurabh Kumar Gupta; Shyam Sundar Kothari
Journal:  Ann Pediatr Cardiol       Date:  2017 Jan-Apr

4.  Isolation of Left Common Carotid Artery with Its Origin Proximal to Patent Ductus Arteriosus Presenting in Adult Age.

Authors:  Anagha R Joshi; Saurabh Joshi; Kiran Kale; Rahul Jain; Jernail Singh Bava
Journal:  Case Rep Radiol       Date:  2016-04-26

5.  External surface anatomy of the postfolding human embryo: Computer-aided, three-dimensional reconstruction of printable digital specimens.

Authors:  Jon Jatsu Azkue
Journal:  J Anat       Date:  2021-07-18       Impact factor: 2.610

  5 in total

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