Results 31 to 40 of about 433 (173)
A Staged Hybrid Approach to an Aberrant Right Subclavian Artery with Symptomatic Kommerell’s Diverticulum [PDF]
Krystal Dinh +3 more
doaj +3 more sources
International multi-institutional experience with presentation and management of aortic arch laterality in aberrant subclavian artery and Kommerell's diverticulum [PDF]
BackgroundAberrant subclavian artery (ASA) with or without Kommerell's diverticulum (KD) is a rare anatomic aortic arch anomaly that can cause dysphagia and/or life-threatening rupture.
Czerny, Martin +3 more
core +5 more sources
An Unusual Cause of Dysphagia: Type II Right-Sided Aortic Arch with Kommerell's Diverticulum [PDF]
Kommerell's diverticulum is an uncommon aortic arch anomaly. Kommerell's diverticulum cases may be asymptomatic, symptoms of compression on the trachea or esophagus may be seen, and these cases also have a risk of spontaneous aortic rupture.
Ayyıldız, Veysel +4 more
core +1 more source
Background: Kommerell's diverticulum with Stanford type A aortic dissection is a relatively rare condition. There is currently no standard treatment strategy for Kommerell's diverticulum. We herein report our surgical strategy with a review of literature
Hisashi Uemura +5 more
doaj +1 more source
Biocellulose patch technique for fetoscopic repair of open spina bifida in twin pregnancy
ABSTRACT Objectives Twin pregnancy is currently an exclusion criterion for prenatal repair of open spina bifida (OSB). The main objective of this study was to report on our experience of treating twin pregnancies with OSB using the skin‐over‐biocellulose for antenatal fetoscopic repair (SAFER) technique.
D. A. Lapa +6 more
wiley +1 more source
ABSTRACT Objectives To evaluate the prenatal characteristics of double aortic arch (DAA), assess the relative size of the arches and their growth during pregnancy, describe associated cardiac, extracardiac and chromosomal/genetic abnormalities and review postnatal presentation and clinical outcome.
M. Bartsota +6 more
wiley +1 more source
Short‐term outcome after the prenatal diagnosis of right aortic arch
Abstract Objectives To determine the proportion of children that require surgery in the first year of life and thereafter in order to improve the counseling of parents with a fetus with a right aortic arch (RAA). Methods Fetuses diagnosed with isolated RAA, defined as the absence of intra‐ or extracardiac anomalies, between 2007 and 2021 were extracted
Bo B. Bet +11 more
wiley +1 more source
Right aortic arch with common origin of right carotid and left innominate artery: A case report
Abstract Aortic arch anomalies are rare congenital malformations with an incidence of approximately 1–3%. Right aortic arch is an anatomical variant with an incidence of <0.1% associated with various congenital heart diseases. We present a case of a 26‐year‐old female patient with a right aortic arch with a common origin of right carotid and left ...
Swati Chand +6 more
wiley +1 more source
Aortosternal Venous Compression: A Review of Two Cases
Aortosternal venous compression (AVC) is a rare venous compression syndrome that involves brachiocephalic venous compression due to its positioning between the sternum and the aorta. One of the features of AVC involves compression of the left innominate vein with variability in luminal caliber on inspiration and expiration.
Victoria Giglio +5 more
wiley +1 more source
We report a patient who presented with acute subclavian chest pain. His work-up revealed a Kommerell's diverticulum coexisting with subclavian artery aneurysm.
Katarzyna Stadnik +3 more
doaj +1 more source

