Anomalous Origin of Bilateral Vertebral Arteries with Retroesophageal Right Subclavian Artery: A Rare Anomaly with Associated Fetal Origin of Bilateral Posterior Cerebral Arteries

2021 ◽  
Vol 69 (6) ◽  
pp. 1844
Author(s):  
ChiragK Ahuja ◽  
Sandeep Moudgil ◽  
Niranjan Khandelwal
Keyword(s):  
Subclavian Artery ◽  
Cerebral Arteries ◽  
Anomalous Origin ◽  
Vertebral Arteries ◽  
Rare Anomaly ◽  
Fetal Origin

Republished: Multiple anomalies in the origin and course of vertebral arteries and aberrant right subclavian artery in a child with moyamoya syndrome

2018 ◽  
Vol 10 (6) ◽  
pp. e14-e14
Author(s):  
Pınar Beyaz ◽  
Nadia Khan ◽  
Gerasimos Baltsavias
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Subclavian Artery ◽  
Anomalous Origin ◽  
Aberrant Right Subclavian Artery ◽  
Moyamoya Syndrome ◽  
Vertebral Arteries ◽  
The Common ◽  
The Right ◽  
First Time

Here we report, for the first time, a combination of five-vessel aortic arch, anomalous origin of the right vertebral artery (VA) from the common carotid artery (CCA), an aberrant right subclavian artery (SCA), and bilateral symmetrical segmental agenesis of VAs.In this case report, we present a patient with moyamoya syndrome (MMS) and Down syndrome (DS) who has bilateral symmetrical segmental agenesis of VAs, left VA originating from aortic arch and anomalous origin of right VA arising from CCA in combination with an aberrant right SCA. Therefore, five vessels are originating from aortic arch. Here, we report, for the first time, a combination of five-vessel aortic arch with an aberrant right SCA and symmetrical segmental agenesis of both VAs. The possible embryological mechanisms of the anomalies as well as an relation with MMS and DS are discussed.

Prenatal diagnosis of anomalous origin of the right pulmonary artery from the ascending aorta

2002 ◽  
Vol 12 (2) ◽  
pp. 186-188 ◽  
Author(s):  
Mi-Jin Jung ◽  
Shi-Joon Yoo
Keyword(s):  
Prenatal Diagnosis ◽  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Fetal Ultrasound ◽  
Cardiac Screening ◽  
Rare Anomaly ◽  
Right Pulmonary Artery ◽  
The Right

We report a case of anomalous origin of the right pulmonary artery from the ascending aorta that was diagnosed by fetal ultrasound at 21 weeks of gestation. The clue to the diagnosis was present in the three-vessel view, this being one of the views that we use for fetal cardiac screening. The anomaly was corrected surgically at 11 days of age. We discuss the importance of prenatal diagnosis in the management of this rare anomaly.

An anomalous origin of the subclavian artery

1915 ◽  
Vol 9 (10) ◽  
pp. 785-789 ◽  
Author(s):  
George Bevier
Keyword(s):  
Subclavian Artery ◽  
Anomalous Origin

scholarly journals Cervical origin of left subclavian artery: A rare anomaly

2014 ◽  
Vol 7 (3) ◽  
pp. 227 ◽  
Author(s):  
PonnusamyShunmuga Sundaram ◽  
Kiron Sukulal ◽  
Sasidharan Bijulal ◽  
JaganmohanA Tharakan
Keyword(s):  
Subclavian Artery ◽  
Left Subclavian Artery ◽  
Rare Anomaly

FEATURES OF HEMODYNAMICS IN HEAD MAGISTRAL AND CEREBRAL ARTERIES IN THE PATIENTS WITH MIGRAINE

2021 ◽  
Vol 74 (10) ◽  
pp. 2489-2493
Author(s):  
Valeriy I. Kalashnikov ◽  
Alexander N. Stoyanov ◽  
Alexander R. Pulyk ◽  
Iryna K. Bakumenko ◽  
Tamara А. Andreeva ◽  
...  
Keyword(s):  
Migraine With Aura ◽  
Migraine Without Aura ◽  
Cerebral Arteries ◽  
Young Patients ◽  
Postgraduate Education ◽  
External Carotid ◽  
Control Group ◽  
Vertebral Arteries ◽  
Hemodynamic Pattern ◽  
Middle Cerebral Arteries

The aim of the study was to Doppler sonography study of the structural and functional state of head magistral arteries (HMA) and cerebral arteries in the patients with various forms of migraine. Materials and methods: We conducted the clinical Doppler examination of 124 young patients (18-45 years old), including 55 men and 69 women in the conditions of the clinical base of the Kharkiv Medical Academy of Postgraduate Education in 2017-2019. The criteria for involvement of patients in the study were: migraine without aura (group 1 – 63 patients), migraine with aura (group 2 – 61 patients) The control group consisted of 45 patients of the corresponding gender and age. The condition of HMA and cerebral arteries was studied using the ultrasound device. Results: The presence of extravasal compressions of vertebral arteries (VA) is typical for the patients with migraine, as well as for some cases of the hypoplasia of the VA in the group of the patients with migraine with aura. In the patients with migraine with aura, there was a decrease in the velocity values in the extracranial VA segments. The velocity values in the external carotid arteries (ECA) were slightly reduced in both groups. The most significant were the changes in the hemodynamics in the middle cerebral arteries (MCA), which were manifested by the pattern of the excessive perfusion in the patients of the migraine without aura and the pattern of the hampered perfusion in the MCA in the patients of the migraine with aura. Conclusions: 1. In the patients with migraine with aura, a decrease in the velocity values in the extracranial segments of the VA was observed, in some cases combined with the hypoplasia of the vertebral artery, the hampered perfusion in middle cerebral arteries. 2. The excessive perfusion in middle cerebral arteries is the most critical hemodynamic pattern in the patients with migraine without aura. 3. The extravasal compression of vertebral arteries, combined with the hyperperfusion in posterior cerebral arteries, is a typical hemodynamic pattern both in the group of the patients with migraine with aura, and in the group of the patients with migraine without aura.

scholarly journals Surgical correction of coarctation of the aorta featuring an incomplete circle of Willis

2020 ◽  
Vol 30 (5) ◽  
pp. 794-795
Author(s):  
Aiko Sonobe ◽  
Hideyuki Kato ◽  
Bryan J Mathis ◽  
Yuji Hiramatsu
Keyword(s):  
Subclavian Artery ◽  
Coarctation Of The Aorta ◽  
Circle Of Willis ◽  
Surgical Correction ◽  
Surgical Strategy ◽  
Aberrant Right Subclavian Artery ◽  
Coarctation Of Aorta ◽  
Rare Anomaly ◽  
Cerebral Malperfusion

Abstract Although devastating complications during simple coarctation of aorta repair now occur less frequently, some unique cases still require extra caution. Here, we report a case of coarctation of the aorta with a rare anomaly in the circle of Willis and an aberrant right subclavian artery, which required a thorough surgical strategy that prevented cerebral malperfusion.

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