1er SEMINAIRE DE CARDIOLOGIE FOE’TALE A PARIS
1er SÉMINAIRE DE CARDIOLOGIE FŒTALE A PARIS
VENDREDI 1 ER FEVRIER 2008
SAMEDI 2 FEVRIER 2008
HÔPITAL ROBERT DEBRÉ
48, boulevard Sérurier
75935 PARIS CEDEX 19
Parma Intern. Echo Meeting ( June 25-26-27 , 2008 )
Don Hagler ( Mayo Clinic ), Steve Sanders ( H. Pediatrico Bambino Gesu’, Roma )
and myself ( Universita’ di Parma ) are glad and proud to present the next Edition of
the Parma Echo Meeting.
The concept of the fetus as a patient
The concept of the fetus as a patient should not be understood in terms of the independent moral status of the fetus, i.e., some feature(s) of the fetus that, independently of other entities e including the pregnant woman, the physician, and the state – generates obligations of others to it.
Hypoplastic left heart syndrome
Hypoplastic left heart syndrome(HLHS) refers to the abnormal development of the left-sided
cardiac structures, resulting in obstruction to blood flow from the left ventricular outflow tract. In
addition, the syndrome includes underdevelopment of the left ventricle, aorta, and aortic arch, as
well as mitral atresia or stenosis…………….>
Cardiac hemangioma during fetal life
Cardiac hemangioma during fetal life
The prevalence of cardiac tumors has been reported to be 0.05% in an autopsy study of infants only. Cardiac hemangioma in infancy is extremely rare and resection of these tumors after prenatal diagnosis has been rarely reported
FETAL AND NEONATAL PRESENTATION OF NON-COMPACTED VENTRICULAR
Noncompaction of the ventricular myocardium (NCVM) is a rare cardiomyopathy characterized by
numerous, prominent trabeculations and deep intertrabecular recesses caused by arrest in myocardial embryogenesis.
This study reviews our experience with neonatal and fetal NCVM. In contrast to the past reports of fetal and
neonatal NCVM, all pts in this group improved, and survived infancy.
ECTOPIA CORDIS : diagnosi prenatale
ECTOPIA CORDIS : diagnosi prenatale
S.Gerboni
L’Ectopia Cordis ( dislocazione parziale o totale del cuore con il suo sacco pericardico fuori dal torace ) è una anomalia congenita altamente letale e fortunatamente estremamente rara : si verifica in 5-8 neonati per un milione di nati vivi. Può essere classificata in quattro tipi a seconda della sede in cui il cuore è dislocato :
– cervicale,
– toracico,
– toraco-addominale
– addominale .
Prenatal diagnosis of persistent left superior vena
Prenatal diagnosis of persistent left superior vena
cava and its associated congenital anomalies
C. BERG*, M. KN¨ UPPEL*, A. GEIPEL*, T. KOHL*, M. KRAPP†, G. KN ¨ OPFLE‡, U. GERMER§, M. HANSMANN* and U. GEMBRUCH*
*Department of Prenatal Medicine and Obstetrics, University of Bonn, and ‡Department of Pathology, Rheinische
Friedrich-Wilhelms-Universit ¨ at, Bonn, †Division of Prenatal Medicine, Department of Obstetrics and Gynecology, University Hospital
Schleswig-Holstein, Campus L¨ ubeck and §Department of Prenatal Medicine, University of Regensburg, Germany
Persistent left superior vena cava (PLSVC) represents the
most common form of anomalous systemic venous return
in adults. It has been observed in 0.3% of autopsies in
the general population and in 4–8% of patients with
congenital heart disease. The PLSVC usually drains into the right atrium via the coronary sinus and may lead to a dilatation of the latter in the prenatal period.