A study in fetuses with prenatally diagnosed single umbilical artery by ultrasonund.
- Author:
Tae Hee KWON
1
;
En Kyung JI
;
Wha Young KIM
;
Do Youn KIM
;
Seok Seon KANG
;
Hye Sun JUN
;
Su Yeon KIM
Author Information
1. Department of Radiology, Obstetrics and Gynecology, College of Medicine, Pochon CHA University, Seoul, Korea. kwonth@cha.ac.kr
- Publication Type:Original Article
- Keywords:
Single umbilical artery;
Congenital anomaly;
Ultrasound
- MeSH:
Choroid Plexus;
Esophageal Atresia;
Female;
Fetus*;
Hernia, Diaphragmatic;
Hernia, Umbilical;
Humans;
Hypoplastic Left Heart Syndrome;
Incidence;
Karyotype;
Medical Records;
Neural Tube Defects;
Pregnancy;
Pregnancy Trimester, Third;
Prognosis;
Pyelectasis;
Single Umbilical Artery*;
Tetralogy of Fallot;
Tracheoesophageal Fistula;
Trisomy;
Ultrasonography
- From:Korean Journal of Obstetrics and Gynecology
2007;50(5):721-725
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: To evaluate the incidence, combined anomaly, and prognosis of prenatally diagnosed Single Umbilical Artery (SUA) by ultrasound. METHODS: From January 2001 to December 2005, a single umbilical artery (SUA) was observed in 41 cases out of 22,868 deliveries. Among 41 cases, 39 cases were examined by targeted imaging to rule out fetal anomalies in the mid trimester (intrauterine pregnancy 16-27 weeks). The remaining two cases were detected in the third trimester, which were transferred from a local clinic, and were examined by routine sonogram. Pregnancy and perinatal outcome data were retrieved by review of the medical records. RESULTS: The incidence of SUA in our population was 0.18%. Of 41 fetuses with SUA, 8 cases presented congenital malformations (19.5%) such as acrania (n=1), Tetralogy of Fallot (n=1), renal anomalies (unilateral renal agenesis n=2, pyelectasis n=1), esophageal atresia (EA) with tracheoesophageal fistula (TEF)(n=1), omphalocele with choroid plexus cyst (CPC)(n=1), and congenital diaphragmatic hernia with hypoplastic left heart syndrome (n=1). Of 33 fetuses with isolated SUA, 3 (9.1%) demonstrated growth restriction. Karyotype analysis was performed in three cases. Two were normal and omphalocele with CPC was Trisomy 18. CONCLUSION: During the prenatal period, the fetus with SUA by ultrasound examination must be carefully monitored with targeted prenatal ultrasound because of its frequent association with fetal congenital anomalies (19.5%). Isolated SUA without associated anomaly dose not affect the outcome of the pregnancy.
