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Prenatal diagnosis of left ventricular aneurysm: a report of three cases and a review

Published online by Cambridge University Press:  19 August 2008

A. Matias
Affiliation:
Department of Developmental Pathology, Hospital Robert Debre, Paris, France
C. Fredouille
Affiliation:
Department of Developmental Pathology, Hospital Robert Debre, Paris, France
C. Nesmann
Affiliation:
Department of Developmental Pathology, Hospital Robert Debre, Paris, France
A. Azancot*
Affiliation:
Prenatal Cardiology Department, Hospital Robert Debre, Paris, France
*
Annabelle Azancot-Benisty MD, PHD, Prenatal Cardiovascular Unit. Service d'Explorations Fonctionnelles, Hospital Robert Debre, 48 Bd Serurier 75019, Paris, France. Tel: 33140032476; Fax: 33140034770; email: [email protected]

Abstract

We report three cases of left ventricular aneurysm diagnosed prenatally and followed by fetal Doppler echocardiography. A review of the literature reveals a paucity of information about this rare cardiac malformation. Most of the described cases (6 out of 9) have remained asymptomatic during pregnancy and after birth. Our cases, in contrast, and three others in the literature, had an ominous prognosis presenting cardiac failure initially or during follow up and showing a dynamic evolution of the aneurysm. Cross-sectional echocardiography provides the diagnosis, revealing the thin-walled aneurysm, usually apical, to be connected by a broad neck to the left ventricle. Color and pulsed Doppler shows low velocity and to-and-fro flow in the aneurysm. Sequential fetal Doppler echocardiography detects the potential growth of the aneurysm relative to ventricular size, revealing any compromise of cardiac performance by a decreased mitral opening, reversed atrial shunting, a hypokinetic infero-posterior left ventricular wall, and a poor systolic thickening of the wall of the aneurysm. Compromise of cardiac function, and deleterious impact on development of the lungs during fetal life, may depend on the early onset, growth and location of the aneurysm, which may occupy most of the fetal chest. We discuss issues of prenatal diagnosis, sequential surveillance of the natural history, and factors of prognosis as well as myocardial histological data from one of our cases.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1999

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