Abstract
Many studies have shown that the prognosis of cystic hygroma associated with hydrops fetalis is poor. We report a rare case of fetal cystic hygroma and hydrops fetalis that spontaneously resolved with subsequent delivery at 37 weeks of a living female infant with Noonan's syndrome. The prognostic significance of prenatal resolution of cystic hygroma and hydrops is uncertain. Serial evaluation of affected fetuses with ultrasound imaging may help clarify pathogenesis of cystic hygroma with associated hydrops, as well as mechanisms underlying spontaneous resolution.
Original language | English |
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Pages (from-to) | 499-502 |
Number of pages | 4 |
Journal | Fetal Diagnosis and Therapy |
Volume | 24 |
Issue number | 4 |
DOIs | |
Publication status | Published - Jan 2009 |
All Science Journal Classification (ASJC) codes
- Pediatrics, Perinatology, and Child Health
- Embryology
- Radiology Nuclear Medicine and imaging
- Obstetrics and Gynaecology