Isolation of a subclavian artery

Nath, P. H.; Castańeda-Zúńiga, W R; Zollikofer, Ch. L.; Delany, David J.; Fulton, Richard E.; Amplatz, Kurt; Edwards, Jan

doi:10.2214/ajr.137.4.683

Cited by 53 publications

(26 citation statements)

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“…Most subclavian isolation was associated with intracardiac [4,[7][8][9][10], aortic arch (interrupted arch [11] or bilateral ductus [12]), or great vessels anomalies [13], most frequently tetralogy of Fallot. All our four patient presented with associated cardiac lesions.…”

Section: Discussionmentioning

confidence: 99%

Isolation of the subclavian artery: 4 cases report and literature review

Chen

Cheng

Lin

et al. 2006

Int J Cardiovasc Imaging

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Section: Discussionmentioning

confidence: 99%

Isolation of the subclavian artery: 4 cases report and literature review

Chen

Cheng

Lin

et al. 2006

Int J Cardiovasc Imaging

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“…In previous case reports, however, (D'Cruz et al 1966;Levine et al 1966;Shaher et al 1972;Pantke et al 1975;Edwards 1977;Karczenski and Wozniewicz 1978;Martin et al 1979;Park 1979;Crump et al 1981;Nath et al 1981;Garti and Aygen 1982;Fong and Venables 1987;Tozzi et al 1989;Ghalili et al 1990;Huang and Wu 1996;Papagiannis et al 1996) the connecting vascular segment between a pulmonary artery and the isolated left common carotid or left innominate artery was interpreted as the left ductus arteriosus (Fig. 1C, D).…”

Section: Chicken Cases Of Isolation Of the Brachiocephalic Arterymentioning

confidence: 91%

“…Among the known congenital anomalies of the aortic arch arteries, a deficient connection (= isolation) of the common carotid or innominate artery to the aorta is rarely found in man. Based on the literature, only four cases with an isolated common carotid artery (Fong and Venables 1987;Tozzi et al 1989;Ghalili et al 1990;Huang and Wu 1996), and twelve cases with an isolated innominate artery (D'Cruz et al 1966;Levine et al 1966;Shaher et al 1972;Pantke et al 1975;Edwards 1977;Karczenski and Wozniewicz 1978;Martin et al 1979;Park 1979;Crump et al 1981;Nath et al 1981;Garti and Aygen 1982;Fong and Venables 1987;Papagiannis et al 1996) are known to us. The analysis of the published data (Table 1) shows three morphological characteristics: (1) If connected to the aorta, the isolated artery would have been the first branch of the aortic arch.…”

Section: Introductionmentioning

confidence: 99%

“…1). Based on these schemes, the isolation of a systemic arch artery from the definitive aorta is explained by abnormal obliterations of specific vascular segments proximal and distal to the respective artery, and connections between a systemic and pulmonary artery are explained by deficient obliteration (persistence) of a right or left ductus arteriosus (D'Cruz et al 1966;Levine et al 1966;Shaher et al 1972;Pantke et al 1975;Edwards 1977;Karczenski and Wozniewicz 1978;Martin et al 1979;Park 1979;Crump et al 1981;Nath et al 1981;Garti and Aygen 1982;Fong and Venables 1987;Tozzi et al 1989;Ghalili et al 1990;Huang and Wu 1996;Papagiannis et al 1996;Fig. 1C, D).…”

Section: Introductionmentioning

confidence: 99%

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

Männer

Seidl

Steding

1997

Anatomy and Embryology

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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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“…Here the LSCA originates from the Left Pulmonary Artery (LPA) rather than the Aortic arch through the ductus arteriosus whether closed or patent [1].…”

Section: Introductionmentioning

confidence: 99%

Isolation of Left Subclavian Artery with Tetralogy of Fallot—A Case Report

Agarwal¹,

Raja²,

Chauhan³

et al. 2017

WJCS

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Background: Isolation of Left Subclavian Artery (LSCA) is a rare subset of Right Aortic Arch (RAA). It is diagnosed as nonvisualization of LSCA in catheterization study. Case Presentation: Here we report an unusual case of Tetralogy of Fallot (TOF) with right aortic arch with isolation of left subclavian artery (LSCA). Here LSCA originated from left pulmonary artery (LPA) through an atretic patent ductus arteriosus (PDA). There was nonvisualization of LSCA in catheterization study and it was confirmed by Computed Tomography (CT) angiography. Re-implantation of LSCA was done to left common carotid artery (LCCA) so that the left upper arm maintains a better flow in the future. Conclusion: Isolation of LSCA especially with TOF is a very rare entity. Re-implantation of LSCA to LCCA was done in view of weak pulses in left upper limb. Results were satisfactory in the follow up period.

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Isolation of a subclavian artery

Cited by 53 publications

References 0 publications

Isolation of the subclavian artery: 4 cases report and literature review

Isolation of the subclavian artery: 4 cases report and literature review

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

Isolation of Left Subclavian Artery with Tetralogy of Fallot—A Case Report

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