We describe a giant bilateral vascular mass in the skin of the chest diagnosed by ultrasound investigation in a fetus of 20 gestational weeks. Ultrasound and colour Doppler investigations detected no signs of early congestive heart failure but rapid and excessive enlargement of the vascular mass. In
PRENATAL ASPECTS OF GIANT FETAL CRANIAL HAEMANGIO-ENDOTHELIOMA
✍ Scribed by PIERRE BOULOT; FRANÇOISE DESCHAMPS; FRANÇOISE MONTOYA; PEDRO MONTOYA; ALAIN COUTURE; JEAN-LOUIS FERRAN; G. LEFORT
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 814 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0197-3851
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✦ Synopsis
A case of a large vascular lesion of the skull is reported. The lesion was discovered at 22 weeks' gestation and it rapidly increased in size, reaching 8 cm a month later. Tumor echogenicity was the same as that for soft tissues and colour Doppler examination revealed intense vascularization. Cordocentesis showed features of the Kasabach-Merritt syndrome and very high plasma levels of alpha-fetoprotein. A Caesarean section was performed to avoid dystocia and led to the birth of a baby with cardiac failure in the immediate neonatal period. Biopsies of the mass led to the diagnosis of a non-malignant haemangio-endothelioma. The mass was removed and plastic surgery performed. The baby is alive and well 9 months after the operation.
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