Results 221 to 230 of about 72,082 (267)
Some of the next articles are maybe not open access.
Archives of Pediatrics & Adolescent Medicine, 1973
Two patients with left cervical aortic arch are presented and are analyzed with the 13 previously reported cases. This anomaly is thought to represent a persistent third embryonic aortic arch with regression of the normal fourth arch. The patient is usually asymptomatic but occasionally has wheezing suggesting a vascular ring.
C M, McCue +3 more
openaire +2 more sources
Two patients with left cervical aortic arch are presented and are analyzed with the 13 previously reported cases. This anomaly is thought to represent a persistent third embryonic aortic arch with regression of the normal fourth arch. The patient is usually asymptomatic but occasionally has wheezing suggesting a vascular ring.
C M, McCue +3 more
openaire +2 more sources
Australasian Radiology, 1956
The history, clinical findings and characteristic radiological features of kinked aortic arch are presented. The condition simulates a mediastinal mass.
openaire +2 more sources
The history, clinical findings and characteristic radiological features of kinked aortic arch are presented. The condition simulates a mediastinal mass.
openaire +2 more sources
Cardiology in the Young, 2019
AbstractAortic arch anomalies are rare congenital cardiovascular malformations. We present a case of a 9-year-old asymptomatic boy with an unusual, unknown arch anomaly.
Pawar RS, Magdum AK, Anderson RH
openaire +3 more sources
AbstractAortic arch anomalies are rare congenital cardiovascular malformations. We present a case of a 9-year-old asymptomatic boy with an unusual, unknown arch anomaly.
Pawar RS, Magdum AK, Anderson RH
openaire +3 more sources
American Journal of Roentgenology, 1975
Cervical aortic arch anomaly is a rare congenital entity. The aortic arch extends into the soft tissues of the neck before turning downward on itself to become the descending aorta. Nineteen cases have been previously reported in the world literature with one more presently in publication.
R, Moncada +5 more
openaire +2 more sources
Cervical aortic arch anomaly is a rare congenital entity. The aortic arch extends into the soft tissues of the neck before turning downward on itself to become the descending aorta. Nineteen cases have been previously reported in the world literature with one more presently in publication.
R, Moncada +5 more
openaire +2 more sources
Annals of Otology, Rhinology & Laryngology, 1992
In conclusion, the diagnosis of DAA should be suspected in an infant with either biphasic stridor or feeding-related respiratory distress. Radiographic studies combined with appropriate thorough endoscopic evaluation should confirm clinical suspicion. Thoracotomy with surgical division of the DAA has given excellent long-term results.
S, Prasad +3 more
openaire +2 more sources
In conclusion, the diagnosis of DAA should be suspected in an infant with either biphasic stridor or feeding-related respiratory distress. Radiographic studies combined with appropriate thorough endoscopic evaluation should confirm clinical suspicion. Thoracotomy with surgical division of the DAA has given excellent long-term results.
S, Prasad +3 more
openaire +2 more sources
Aortic Arch Anomalies: Aortic Arch Interruption
2021The interrupted aortic arch is very rare and occurs in about 1% of the infants with critical congenital heart disease. Perfusion distal to the interruption is dependent on the patency of the ductus arteriosus. Unrecognized and untreated cases have a median age of death at 4–10 days of life.
Elisa Rhee, Dilachew A. Adebo
openaire +1 more source
Archives of Surgery, 1969
Arteriosclerotic occlusion of the great vessels arising from the aortic arch was initially described by Savory1in 1856. Hunt,2in 1914, pointed out that extracranial obstruction of the carotid arteries could cause stroke. Introduction of arteriographic techniques by Egas-Moniz et al3in 1937 made accurate diagnosis of these lesions possible.
B W, Thompson, R C, Read, G S, Campbell
openaire +2 more sources
Arteriosclerotic occlusion of the great vessels arising from the aortic arch was initially described by Savory1in 1856. Hunt,2in 1914, pointed out that extracranial obstruction of the carotid arteries could cause stroke. Introduction of arteriographic techniques by Egas-Moniz et al3in 1937 made accurate diagnosis of these lesions possible.
B W, Thompson, R C, Read, G S, Campbell
openaire +2 more sources
Postgraduate Medicine, 1967
Since many aortic arch lesions are amenable to surgical treatment, aortography has assumed greater importance.
R J, Marshall, L T, Mouser
openaire +2 more sources
Since many aortic arch lesions are amenable to surgical treatment, aortography has assumed greater importance.
R J, Marshall, L T, Mouser
openaire +2 more sources
International Journal of Stroke, 2006
Severe atheroma of the aortic arch has now been established as an important risk factor and mechanism for stroke and peripheral embolism. The odds ratio for stroke or peripheral embolism in patients with severe arch atheroma is greater than four, and for mobile atheroma it is greater than 12.
Jorge A, Zavala +7 more
openaire +2 more sources
Severe atheroma of the aortic arch has now been established as an important risk factor and mechanism for stroke and peripheral embolism. The odds ratio for stroke or peripheral embolism in patients with severe arch atheroma is greater than four, and for mobile atheroma it is greater than 12.
Jorge A, Zavala +7 more
openaire +2 more sources
Aortic Arch Coarctation and Interrupted Aortic Arch
2014The proximal aortic arch is the beginning part of the innominate artery; the distal aortic arch is the isthmus where the ligamentum arteriosum is attached and is also the starting point of the descending thoracic aorta. In the embryonic stage, the aortic arch initially is paired and later turns into a single aortic arch (lactation type). Therefore, the
openaire +1 more source