Abstract
The failure of embryonic vascular arches to fuse and regress in the usual manner during the formation of the aortic arch, pulmonary arteries and ductus arteriosus can cause a wide spectrum of vascular congenital abnormalities of the aortic arch and its branches. These abnormal vascular structures may cause variable compression of the trachea and/or oesophagus with symptoms ranging from none to severe stridor, dyspnoea, dysphagia and cyanosis. Diagnosis and possible treatment of affected patients require multiple imaging modalities. In the majority of cases, the underlying malformation can be detected by chest radiography and barium oesophagography, visualizing the location of the aortic arch and the presence of anomalous compressions of the trachea and/or oesophagus. However, in most cases the exact configuration of the vascular abnormality cannot be fully defined with conventional radiology alone. MRI is fundamental for evaluation of the thoracic vessels. Not only is it non-invasive, but it can also provide large-field-of-view images in any number of planes with three-dimensional reconstruction, adding valuable information about exact vascular configuration, tracheobronchial compression and brachiocephalic vessel branching. The aim of this review is to describe the imaging findings in children affected with special emphasis on MRI.
Original language | English |
---|---|
Pages (from-to) | 947-960 |
Number of pages | 14 |
Journal | Pediatric Radiology |
Volume | 35 |
Issue number | 10 |
DOIs | |
Publication status | Published - Oct 2005 |
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Keywords
- Aorta
- Arteries
- Congenital malformation
- MRI
- Radiography
- Vascular ring
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
- Pediatrics, Perinatology, and Child Health
- Radiological and Ultrasound Technology
Cite this
Multi-modality evaluation of the abnormalities of the aortic arches in children : Techniques and imaging spectrum with emphasis on MRI. / Oddone, Mauro; Granata, Claudio; Vercellino, Nadia; Bava, Erica; Tomà, Paolo.
In: Pediatric Radiology, Vol. 35, No. 10, 10.2005, p. 947-960.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Multi-modality evaluation of the abnormalities of the aortic arches in children
T2 - Techniques and imaging spectrum with emphasis on MRI
AU - Oddone, Mauro
AU - Granata, Claudio
AU - Vercellino, Nadia
AU - Bava, Erica
AU - Tomà, Paolo
PY - 2005/10
Y1 - 2005/10
N2 - The failure of embryonic vascular arches to fuse and regress in the usual manner during the formation of the aortic arch, pulmonary arteries and ductus arteriosus can cause a wide spectrum of vascular congenital abnormalities of the aortic arch and its branches. These abnormal vascular structures may cause variable compression of the trachea and/or oesophagus with symptoms ranging from none to severe stridor, dyspnoea, dysphagia and cyanosis. Diagnosis and possible treatment of affected patients require multiple imaging modalities. In the majority of cases, the underlying malformation can be detected by chest radiography and barium oesophagography, visualizing the location of the aortic arch and the presence of anomalous compressions of the trachea and/or oesophagus. However, in most cases the exact configuration of the vascular abnormality cannot be fully defined with conventional radiology alone. MRI is fundamental for evaluation of the thoracic vessels. Not only is it non-invasive, but it can also provide large-field-of-view images in any number of planes with three-dimensional reconstruction, adding valuable information about exact vascular configuration, tracheobronchial compression and brachiocephalic vessel branching. The aim of this review is to describe the imaging findings in children affected with special emphasis on MRI.
AB - The failure of embryonic vascular arches to fuse and regress in the usual manner during the formation of the aortic arch, pulmonary arteries and ductus arteriosus can cause a wide spectrum of vascular congenital abnormalities of the aortic arch and its branches. These abnormal vascular structures may cause variable compression of the trachea and/or oesophagus with symptoms ranging from none to severe stridor, dyspnoea, dysphagia and cyanosis. Diagnosis and possible treatment of affected patients require multiple imaging modalities. In the majority of cases, the underlying malformation can be detected by chest radiography and barium oesophagography, visualizing the location of the aortic arch and the presence of anomalous compressions of the trachea and/or oesophagus. However, in most cases the exact configuration of the vascular abnormality cannot be fully defined with conventional radiology alone. MRI is fundamental for evaluation of the thoracic vessels. Not only is it non-invasive, but it can also provide large-field-of-view images in any number of planes with three-dimensional reconstruction, adding valuable information about exact vascular configuration, tracheobronchial compression and brachiocephalic vessel branching. The aim of this review is to describe the imaging findings in children affected with special emphasis on MRI.
KW - Aorta
KW - Arteries
KW - Congenital malformation
KW - MRI
KW - Radiography
KW - Vascular ring
UR - http://www.scopus.com/inward/record.url?scp=26044483592&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=26044483592&partnerID=8YFLogxK
U2 - 10.1007/s00247-005-1436-4
DO - 10.1007/s00247-005-1436-4
M3 - Article
C2 - 15973515
AN - SCOPUS:26044483592
VL - 35
SP - 947
EP - 960
JO - Pediatric Radiology
JF - Pediatric Radiology
SN - 0301-0449
IS - 10
ER -