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A rare case of right aortic arch with mirror-image branching and vascular ring in an adult patient [PDF]

open access: yesRadiology Case Reports
A right-sided aortic arch with mirror-image branching is a rare vascular anomaly, often associated with congenital heart defects. However, its occurrence with a vascular ring in the absence of cardiac abnormalities is extremely rare.
Salma El Aouadi   +5 more
doaj   +7 more sources

Right aortic arch with mirror image branching found incidentally during coronary surgery [PDF]

open access: yesSAGE Open Medical Case Reports, 2021
Right aortic arch with a left innominate (brachiocephalic) artery with mirror image branching (RAMI) is a rare congenital anomaly, and it is unusual to diagnose it in adulthood.
Girish N Rao   +5 more
doaj   +5 more sources

Right aortic arch with mirror image branching pattern and isolated left brachiocephalic artery: A case report [PDF]

open access: yesRadiology Case Reports, 2020
We present a very rare case of right aortic arch with an isolated left brachiocephalic artery in a 35-year-old female. This entity is an extremely uncommon aortic arch anomaly which has associated multisystem symptoms. We briefly discuss the hypothetical
Ayman Nada, MD, PhD   +3 more
doaj   +6 more sources

Transcatheter aortic valve replacement in right aortic arch with mirror image branching [PDF]

open access: yesBMC Cardiovascular Disorders
Background A right aortic arch withmirror-image branching is a rare congenital anomaly resulting from the abnormal regression ofthe embryonic left aortic arch.
Prem Patel   +2 more
doaj   +5 more sources

Right-sided aortic arch with mirror image branching and situs solitus: a case of a 79 years old woman [PDF]

open access: yesRadiology Case Reports, 2019
Right aortic arch with mirror image branching (RAMI) is a rare congenital defect of the aorta. The exact incidence of RAMI in the general population is unclear. In RAMI the first branch arising from the arch is the left innominate artery, followed by the
Daniele Morosetti, MD   +7 more
doaj   +6 more sources

Imaging findings in the right aortic arch with mirror image branching of arch vessels: An unusual cause of dysphagia

open access: yesMedical Journal of Dr. D.Y. Patil University, 2015
We report a case of a 72-year-old female with a right aortic arch with mirror-image branching of arch vessels presenting with dysphagia, and characteristic images on barium esophagogram, contrast-enhanced computed tomography scan, and magnetic resonance ...
Guneet Singh   +3 more
doaj   +3 more sources

A Rare Vascular Ring Malformation Formed by Right Aortic Arch With Mirror Image Branching Causing Dysphagia: Case Report [PDF]

open access: yesClinical Case Reports
A right‐sided aortic arch, a congenital anomaly of the aortic arch, was initially described by Fioratti and Aglietti in 1963. This condition, associated with formation of a vascular ring, can constrict mediastinal organs such as the trachea and esophagus.
Md. Deluwar Hussen   +5 more
doaj   +3 more sources

A Rare Case of Right-Sided Aortic Arch With Mirror-Image Branching and Congenital Absence of the Left Pulmonary Artery [PDF]

open access: yesCureus, 2023
Both the right-sided aortic arch with mirror-image branching (RAMI) and the congenital absence of the left pulmonary artery are sporadic congenital defects. Both diseases are typically diagnosed in childhood, but occasionally asymptomatic cases may be incidentally detected through imaging in adulthood.
Shtembari, Jurgen   +3 more
openaire   +3 more sources

Complete Vascular Ring Caused by Kommerell's Diverticulum and Right Aortic Arch with Mirror Image Branching [PDF]

open access: yesThe Korean Journal of Thoracic and Cardiovascular Surgery, 2012
Vascular ring, caused by Kommerell's diverticulum and ligamentum arteriosum, in a patient with right aortic arch and mirror image branching is extremely rare. A 10-month-old boy with coughing and stridor was diagnosed as having tracheo-esophageal stenosis, which is caused by a vascular ring with Kommerell's diverticulum, ligamentum arteriosum, right ...
Ryu JW.
openaire   +3 more sources

Congenital cystic adenomatoid malformation associated with right aortic arch with mirror image branching and absence of left pulmonary artery in an adult [PDF]

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2021
Background Congenital cystic adenomatoid malformation is an uncommon developmental anomaly that is diagnosed prenatally or during early childhood and is rare to present in adulthood.
Elamparidhi Padmanaban   +4 more
doaj   +2 more sources

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