PERSISTING SPONGY MYOCARDIUM - A CASE INDICATING THE DIFFICULTY OF ANTENATAL DIAGNOSIS

Citation
N. Winer et al., PERSISTING SPONGY MYOCARDIUM - A CASE INDICATING THE DIFFICULTY OF ANTENATAL DIAGNOSIS, Fetal diagnosis and therapy, 13(4), 1998, pp. 227-232
Citations number
12
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
10153837
Volume
13
Issue
4
Year of publication
1998
Pages
227 - 232
Database
ISI
SICI code
1015-3837(1998)13:4<227:PSM-AC>2.0.ZU;2-E
Abstract
Persisting spongy myocardium (also known as noncompaction of the ventr icular myocardium) is a rare and special form of cardiomyopathy. The f ew cases reported in the literature were detected postnatally and invo lved a high rate of cardiovascular complications. This anomaly of endo myocardial morphogenesis, which occurs during the embryonic phase at t he stage of cardiac partitioning, is characterised by an excessive num ber of prominent trabeculae and by intertrabecular recesses within the myocardial wall. Antenatal detection is difficult in the absence of a n associated malformation, which is the general situation. We report a case of antenatal cardiomyopathy which led to therapeutic abortion. T he diagnosis of persisting spongy myocardium was made during fetopatho logic examination.