Klippel–Trenaunay–Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis
✍ Scribed by Dr L. F. Gonçalves; M. V. Muñoz Rojas; D. Vitorello; E. Ternes Pereira; M. Pereima; J. A. Saab Neto
- Book ID
- 114434541
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 84 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0960-7692
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract This report describes the prenatal sonographic diagnosis of a case of Klippel‐Trénaunay‐Weber syndrome. The sonographic appearance of this disorder was characterized by the presence of multiple distorted cystic areas involving the right leg and abdomen and cardiomegaly with early fetal
Klippel-Trenaunay-Weber syndrome is a complex developmental disorder characterized by a triad of cutaneous haemangioma, varicosities of the body, and unilateral limb hypertrophy. We describe the prenatal diagnosis of Klippel-Trenaunay-Weber syndrome at 15 weeks' gestation using the surface rendering
Ultrasound examination led to prenatal diagnosis of Klippel-Trénaunay-Weber syndrome complicated by early fetal congestive heart failure. The postnatal course was complicated by the Kasabach-Merritt syndrome of thrombocytopenia due to platelet consumption within the haemangioma. There was need for n