The case of a young child who demonstrated extrinsic narrowing of the thoracich trachea related to a mediastinal bronchogenic cyst is reported. Diagnosis was made by magnetic resonance imaging. About this case report, the authors review the possible causes of tracheal narrowing at this age of life and suggest a simple diagnostic management protocol.

A case of supracardiac total anomalous pulmonary venous drainage (TAPVD) in an infant aged 2 1/2 months is presented. Diagnosis was established non invasively by magnetic resonance image (MRI). Not only did MRI precisely depict the anomalous venous pathway but it moreover securely excluded pulmonary venous obstruction.

The case of a young child who demonstrated extrinsic narrowing of the thoracich trachea related to a mediastinal bronchogenic cyst is reported. Diagnosis was made by magnetic resonance imaging. About this case report, the authors review the possible causes of tracheal narrowing at this age of life and suggest a simple diagnosic management protocol.

Between February 1988 and July 1989, the authors used magnetic resonance imaging (MRI) to study 54 newborn infants aged between 2 and 35 days and suspected of congenital heart disease. All children also underwent echocardiography and 7 angiography during the neonatal period (13% of children studied). MRI was well tolerated and there were no adverse events. MRI proved to be complementary to echocardiography in several lesions affecting the great vessels of the base and the left atrial region. Agreement between angiography and MRI results was very good, with MRI being more useful in one case. MRI enables full and non-invasive postoperative follow-up. In conclusion, despite the great heterogenicity of the cardiac malformations studied and which requires a degree of caution, the authors feel that MRI is a second line investigation after echocardiography. It may limit the indications of angiography. Its own indications are the retrocardiac region, the main arteriovenous vessels of the base and postoperative follow-up in congenital heart disease. The development of techniques such as angio RM will further modify data in the future.

Between February 1988 and July 1989, the authors used magnetic resonance imaging (MRI) to study 54 newborn infants aged between 2 and 35 days and suspected of congenital heart disease. All children also underwent echocardiography and 7 angiography during the neonatal period (13% of children studied). MRI was well tolerated and there were no adverse events. MRI proved to be complementary to echocardiography in several lesions affecting the great vessels of the base and the left atrial region. Agreement between angiography and MRI results was very good, with MRI being more useful in one case. MRI enables full and non-invasive postoperative follow-up. In conclusion, despite the great heterogenicity of the cardiac malformations studied and which requires a degree of caution, the authors feel that MRI is a second line investigation after echocardiography. It may limit the indications of angiography. Its own indications are the retrocardiac region, the main arteriovenous vessels of the base and postoperative follow-up in congenital heart disease. The development of techniques such as angio RM will further modify data in the future.

Schlüsselwörter Kernspintomographie - Pulmonalatresie mit Ventrikelseptumdofckt - Arteria lusoria - Blalock–Taussig

The authors report the case of a 3-month-old infant with a history of interventricular septal defect with pulmonary arterial hypertension. This child had pulmonary symptomatology (dyspnea, recurrent bronchitis, acute attacks of asphyxia) which it was possible to link to a retrotracheal left pulmonary artery by magnetic resonance imaging (MRI). Classical investigations (upper GI barium series and chest X-ray) were suggestive of a bronchogenic cyst type abnormal pulmonary structure. Angiography confirmed the MRI diagnosis. In this case the infant also had tracheal lesions (lower tracheal hypoplasia) which required further evaluation by fibroscopy and bronchography. Thus MRI shows itself to be a useful investigation in the study of basic vascular abnormalities.

Until now little attention has been paid to the potential of MR imaging in congenital heart disease of the newborn. ECG-gated MRI was therefore performed at 0.5 tesla in 23 newborns (mean age 7.5 days) with suspected congenital heart disease. Two newborns were controlled after surgery (switch, Blalock-Taussig procedure). All had undergone prior evaluation by two-dimensional Doppler echocardiography (2-D DE). MR imaging was of a satisfying quality in all but one newborn. The aim of this study was to assess complementary information provided by MRI in comparison to 2-D DE. Pre-operatively MRI missed some abnormalities shown by 2-D DE: one coartaction, one ductus arteriosus and one pulmonary atresia. MRI demonstrated lesions that echocardiography had either failed to visualize or found inconclusive, including double aortic arch (one patient), muscular ventricular septum defect (two patients) and severe ductus arteriosus (one patient). In one of the two patients with a ventricular septum defect, angiography was avoided and in the other patient it merely confirmed the MRI results. Post-operatively, MRI demonstrated information complementary to that obtained from to 2-D DE: (1) clearly visualizing the reinsertion of the coronary arteries in the ‘switched’ transposition of the great vessels, (2) appreciating the diameter and patency of the palliative shunt in the Blalock-Taussig procedure.

The authors report the case of a 34 weeks premature infant presenting a transpositions of the large vessels, who underwent a Rashkind during the neonatal period, a Senning procedure at three months, and was explored and followed-up by magnetic resonance imaging (MRI). The images obtained are of good quality, permitting a precise diagnosis of transposition of the large vessels and visualization of an inter-ventricular communication (IVC) which were missed on ultrasonography. The MRI shows complete images of the Senning correction and permits a non-invasive post-operative monitoring of this correction. MIR is therefore an interesting second intention examination which may effectively complement ultrasonography and limit the indications of angiography.

The aim of this study was to evaluate potential indications of Magnetic Resonance Imaging (MRI) in the diagnostic workup of congenital heart disease in the newborn in comparison with two other means of investigation: Doppler-echocardiography and angiography. The imaging permitted to make the diagnosis in the 10 cases. MRI was superior than echocardiography in one newborn with a double aortic arch. MRI detected small muscular ventricular septum defects in two newborns with transposition of the great vessels. There was good agreement between MRI and angiographic images. Neither age nor prematurity proved to pose a limit on the diagnosis of MRI. MRI proved to be a good investigative tool which should be used after echocardiography, eventually making it possible to avoid angiography.

The authors report a case of double aortic arch in the newborn (age: 1 month) explored with magnetic resonance imaging. MRI offers a non invasive and non ionizing examination very well-tolerated by the patient if a correct methodology is used (total acquisition time 40 mn). The quality of the images is sufficient for diagnosis and presurgical evaluation: the diameter, the permeability and the relationship with the surrounding organs of the respective aortic arches were well demonstrated with this technique. The contributions of MRI with respect to 2-D echocardiography and angiography as well as the future possible totally non invasive evaluation of this cardiac anomaly is discussed.