Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Pediatr Cardiol ; 12(1): 57-9, 1991 Jan.
Article in English | MEDLINE | ID: mdl-1997987

ABSTRACT

An intrapericardial mass with a pericardial effusion was diagnosed by ultrasound examination in the fetus of a 29-year-old gravida 1 para 0 woman at 32 weeks' gestation. Serial in utero examinations showed disappearance of the pericardial effusion at 35.5 weeks' gestation, while the mass remained unchanged. Vaginal delivery ensued at 39 weeks. Clinical and echocardiographic examination of the newborn revealed normal cardiac anatomy with no abnormal mass or pericardial effusion. Follow-up examinations confirmed these normal data.


Subject(s)
Echocardiography , Heart Neoplasms/diagnostic imaging , Hemangioma, Cavernous/diagnostic imaging , Pericardial Effusion/etiology , Teratoma/diagnostic imaging , Ultrasonography, Prenatal/methods , Adult , Female , Humans , Pericardial Effusion/diagnostic imaging , Pregnancy , Thrombosis/complications , Thrombosis/diagnostic imaging
2.
Cardiol Young ; 8(1): 134-5, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9680288

ABSTRACT

Cardiac rhabdomyoma is a rare tumor. Because of its rate of regression, mainly in the first year of life, conservative therapy is generally suggested when diagnosis occurs in infancy. We report surgical ablation of a rhabdomyoma in a 2-month-old boy in whom the tumor extended into the subaortic outflow tract. The tumor, which had a dual attachment to the aortic and mitral valves, was safely removed without any valvar damage. We suggest immediate surgical intervention for those rhabdomyomas which are life-threatening because of their size, location, or arrhythmogenicity.


Subject(s)
Heart Neoplasms/surgery , Rhabdomyoma/surgery , Tuberous Sclerosis/complications , Heart Neoplasms/etiology , Humans , Infant , Male , Rhabdomyoma/etiology
3.
J Pediatr ; 121(4): 608-13, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1403399

ABSTRACT

The purpose of this study was to evaluate the efficacy of maternal digoxin administration in 16 cases of fetal supraventricular tachyarrhythmia diagnosed by fetal echocardiography; cardiac anatomy was normal in all cases. The retrospective analysis included nine mothers who received digoxin orally in most cases, with control of the arrhythmia in two fetuses. The addition of amiodarone (five cases) and propranolol (two cases) yielded two successes with amiodarone. The therapeutic regimen of digoxin was then modified on the basis of poor response to orally administered digoxin. In the prospective study, digoxin was administered intravenously to seven mothers according to a standard protocol; high doses (1 to 2 mg intravenously) were prescribed for the first 24 hours and intravenous digoxin therapy was maintained for at least 5 days, depending on the fetal response. Digoxin pharmacokinetic studies of four mothers showed an increased plasma clearance and reduced elimination half-life. Digoxin controlled the five supraventricular tachycardias (with hydrops in four cases). Maternal flecainide therapy restored sinus rhythm in two cases of atrial flutter. Our prospective study emphasizes the efficacy and safety for the fetus and the mother of intravenously administered digoxin as a first-choice drug in the treatment of supraventricular tachyarrhythmias. Flecainide may be a promising second-choice drug but requires further clinical investigation. Amiodarone and propranolol seem to be ineffective.


Subject(s)
Digoxin/therapeutic use , Fetal Diseases/drug therapy , Tachycardia, Supraventricular/drug therapy , Digoxin/pharmacokinetics , Drug Therapy, Combination , Flecainide/therapeutic use , Humans , Prospective Studies , Retrospective Studies
SELECTION OF CITATIONS
SEARCH DETAIL