Prenatal diagnosis of double aortic arch and D-transposition of the great arteries: a case report

2010 ◽  
Vol 30 (4) ◽  
pp. 382-383
Author(s):  
W. M. Yao ◽  
J. M. Wang ◽  
H. F. Huang ◽  
Y. H. Ye
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Aortic Arch ◽  
Double Aortic Arch

scholarly journals Isolated Double Aortic Arch (Daa) – Prenatal Detection with Postnatal Follow-Up, Case Report and Literature Review

2018 ◽  
Vol 8 (1) ◽  
pp. 64-70
Author(s):  
Julia Murlewska ◽  
Agnieszka Żalińska ◽  
Danuta Roik ◽  
Bożena Werner ◽  
Maria Respondek-Liberska
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Literature Review ◽  
Aortic Arch ◽  
Clinical Symptoms ◽  
Double Aortic Arch ◽  
Computer Reconstruction ◽  
Prenatal Detection ◽  
Angio Ct

Abstract This case report presents a prenatal diagnosis with postnatal confirmation (by angio CT and computer reconstruction) of an isolated double aortic arch, with no blood disturbances and with no clinical symptoms after birth. Literature review was focusing on the possible symptoms in the future. Prenatal findings should be forwarded to neonatologist and pediatrician despite clinical silence.

Prenatal Diagnosis of Double Aortic Arch

2021 ◽  
Author(s):  
Helen Bornaun ◽  
Sema Süzen Çaypınar ◽  
Zeynep Gedik Özköse ◽  
Nura Fitnat Topbaş ◽  
Mustafa Behram
Keyword(s):  
Prenatal Diagnosis ◽  
Aortic Arch ◽  
Double Aortic Arch

scholarly journals P725 An unexpected direction: a case report of a double aortic arch in an asymptomatic woman in adulthood

2020 ◽  
Vol 21 (Supplement_1) ◽  
Author(s):  
I Campos ◽  
C Vieira ◽  
N Salome ◽  
V H Pereira ◽  
A Costeira Pereira ◽  
...  
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Ct Angiography ◽  
Vascular Ring ◽  
Double Aortic Arch ◽  
Posterior Arch ◽  
Vascular Rings ◽  
Thoracic Ct ◽  
Extrinsic Compression ◽  
The Right

Abstract Introduction Complete vascular rings represent about 0.5-2% of all congenital cardiovascular malformations, with the double aortic arch (DAA) being the most common of the complete vascular rings, causing tracheoesophageal compression. The right (posterior) arch is usually dominant (70%), although the two arches can have the same size (5%). The left (anterior) arch is dominant in only approximately 25% of cases. In most cases, this anomaly is diagnosed during childhood due to symptoms caused by oesophageal or tracheal compression. For this reason, case reports of adults are rare. This report describes a case of a 61-year-old woman with DAA with dominant left arch, diagnosed accidentallyby thoracic CT angiography. Case Report Description A 61 years old woman with a previous story of hypertension and type 1 diabetes presented to the emergency service with dyspnoea and thoracic pain. She also referred a history of intermittent dysphagia and cough with at least 12 years of progression. All the parameters of the physical examination were within normal limits. The electrocardiogram showed a normal sinus rhythm with no evidence of acute ischemia and her blood analyses did not show any abnormalitie. She also performed a thoracic CT angiography, which excluded signs of pulmonary embolism, but revealed a vascular ring suggesting a double aortic arch with permeability in both right and left arches as well as their collaterals. The Cardiac MRI was performed with the purpose of excluding ischemia, confirming the double aortic arch with left dominance. The right arch, posterior to the oesophagus and trachea, and the left arch, in an anterior position, showed an anatomic compression of the oesophagus as well as the proximal trachea, capable of eliciting the symptoms mentioned. Other congenital anomalies were excluded. The echocardiography did not demonstrate any additional cardiac malformation. Endoscopy shows a pulsatile extrinsic compression of the esophagus (aortic ring). The patient is currently being studied and closely monitored in the Cardiology consultation. Discussion The most common type of complete vascular ring is the double aortic arch, which accounts for 70% of the complete rings. In most cases, there are two permeable arches, usually with right dominance (70% of the cases). Rarely, both arches are symmetrical. Symptoms usually appear in the fifth month of life. In most cases, only supportive treatment is required. Conclusion This case illustrates the atypical features of this congenital malformation, namely the diagnosis during adulthood as well as the left dominance. Abstract P725 Figure. A double aortic arch

Pierre Robin sequence and double aortic arch: a case report

2005 ◽  
Vol 69 (1) ◽  
pp. 105-110 ◽  
Author(s):  
Edward T. Waters ◽  
James P. Oberman ◽  
Abhik K. Biswas
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Double Aortic Arch ◽  
Pierre Robin Sequence ◽  
Robin Sequence ◽  
Pierre Robin

A functioning double aortic arch in an infant: A case report

1994 ◽  
Vol 24 (1) ◽  
pp. 76-77 ◽  
Author(s):  
F. Machiels ◽  
M. de Maeseneer ◽  
B. Desprechins ◽  
M. Osteaux ◽  
D. Dewolf
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Double Aortic Arch

scholarly journals Prenatal diagnosis of the rare association of common arterial trunk and double aortic arch

2016 ◽  
Vol 4 (7) ◽  
pp. 668-670 ◽  
Author(s):  
Andrea Rock ◽  
Osama Eltayeb ◽  
Joseph Camarda ◽  
Nina Gotteiner
Keyword(s):  
Prenatal Diagnosis ◽  
Aortic Arch ◽  
Double Aortic Arch ◽  
Rare Association ◽  
Common Arterial Trunk ◽  
Arterial Trunk
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