scholarly journals Congenital defect of the posterior arch of C1: a case report

2021 ◽  
Vol 7 (2) ◽  
pp. 214-217
Author(s):  
Bilal B. Butt ◽  
Paul Gagnet ◽  
Rakesh Patel ◽  
Ilyas Aleem
2007 ◽  
Vol 42 (4) ◽  
pp. 559 ◽  
Author(s):  
Chang Hoon Jeon ◽  
Gu Young Chung ◽  
Nam Su Chung ◽  
Un-Seup Jeoung ◽  
Dong-hyun Lee ◽  
...  

2020 ◽  
Vol 21 (Supplement_1) ◽  
Author(s):  
I Campos ◽  
C Vieira ◽  
N Salome ◽  
V H Pereira ◽  
A Costeira Pereira ◽  
...  

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


1993 ◽  
Vol 42 (2) ◽  
pp. 615-617
Author(s):  
Yoichiro Iwamatsu ◽  
Etsuji Shiota ◽  
Naoyuki Tomokane
Keyword(s):  

2015 ◽  
Vol 64 ◽  
pp. S62
Author(s):  
B.S. Prakash ◽  
K. Padmalatha ◽  
Mahalakshmi Chitragar
Keyword(s):  

1977 ◽  
Vol 23 (1) ◽  
pp. 138-143
Author(s):  
Takeshi HONDA ◽  
Yasuomi NAKASHIMA ◽  
Haruhiko NAGAI ◽  
Kasuke NAKAJIMA ◽  
Katsuma KOMOTO

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