Results 71 to 80 of about 600 (153)

Case Report: Unlocking arteria Lusoria challenges: sternotomy's role in a single-stage aneurysm repair and artery realignment

open access: yesFrontiers in Cardiovascular Medicine
Arteria lusoria (AL), an anomaly of the right subclavian artery, occurs in 2% of individuals and can cause symptoms such as dysphagia due to its retroesophageal course.
Ziyad Gunga   +10 more
doaj   +1 more source

Dysphagia Lusoria Caused by an Aberrant Right Subclavian Artery

open access: yesThe Korean Journal of Gastroenterology, 2022
Hee Jin Kim, Hyun Jin Kim
doaj   +1 more source

Aberrant right subclavian artery: A review

open access: yesJVS-Vascular Insights
Aberrant subclavian artery is a rare condition, with patients often present with dysphagia, dyspnea, back pain, or upper limb ischemia; occasionally, the condition is incidentally discovered as a mediastinal mass on chest radiography.
Ilayakumar Paramasivam, Mch   +6 more
doaj   +1 more source

The Aberrant Right Subclavian Artery as Incidental Finding and Associated to Dysphagia. A series of Cases and Review of the Literature

open access: yesSwiss Journal of Radiology and Nuclear Medicine
The Aberrant right subclavian artery (ARSA), also known as the "arteria lusoria," is a distinctive congenital anomaly of the aortic arch. Its estimated prevalence in the general population ranges from 0.16% to 4.4%, with a higher incidence in women ...
Ilson Sepúlveda   +3 more
doaj   +1 more source

Dysphagia Lusoria in Twins [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
R Hariharaprakas, Padma Badhe, Amit Dey
doaj   +1 more source

Dysphagia Lusoria Causing Aspiration Pneumonitis in a Patient With Recurrent Pancreatitis. [PDF]

open access: yesCureus, 2022
Adithya Sateesh B   +4 more
europepmc   +1 more source

A Rare Aortic-Arch Variant – Arteria Lusoria: Case Report with Review of Literature and Clinical Implications

open access: yesActa Medica Bulgarica
The aberrant right subclavian artery (arteria lusoria, AL) is the most common aortic-arch branching variant, occurring in approximately 0.5–2.5% of the population.
Gaydarski L.   +3 more
doaj   +1 more source

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