HYPEREOSINOPHILIC SYNDROME IN A TRISOMY-21 FETUS

Citation
Y. Kusanagi et al., HYPEREOSINOPHILIC SYNDROME IN A TRISOMY-21 FETUS, Obstetrics and gynecology, 92(4), 1998, pp. 701-702
Citations number
8
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
00297844
Volume
92
Issue
4
Year of publication
1998
Part
2
Supplement
S
Pages
701 - 702
Database
ISI
SICI code
0029-7844(1998)92:4<701:HSIATF>2.0.ZU;2-#
Abstract
Background: Hypereosinophilic syndrome is characterized by peripheral blood eosinophilia and multiple organ system involvement. Only one cas e in a newborn has been reported. Case: Fetal sonography performed on a 33-year-old woman at 35 weeks' gestation showed pericardial effusion and cardiomegaly. The infant was delivered by cesarean at 35 weeks' g estation because of a worsening of the pericardial effusion. Hematolog ic studies revealed unexplained hypereosinophilia, and the pericardial fluid contained a large number of eosinophils. Chromosomal analysis r evealed trisomy 21. The hypereosinophilia, pericardial effusion, and c ardiomegaly all resolved after 8 weeks of steroid therapy. Conclusion: Hypereosinophilic syndrome caused pericardial effusion and cardiomega ly in a fetus with trisomy 21. (Obstet Gynecol 1998;92:701-2. (C) 1998 by The American College of Obstetricians and Gynecologists.).