MRI assessment of fetal autosomal recessive polycystic kidney disease
10.3760/cma.j.issn.1005-1201.2014.12.003
- VernacularTitle:常染色体隐性遗传性多囊肾病胎儿的MRI表现
- Author:
Suzhen DONG
;
Ming ZHU
;
Yumin ZHONG
;
Hong ZHANG
;
Huihong PAN
- Publication Type:Journal Article
- Keywords:
Polycystic kidney,autosomal recessive;
Fetus;
Magnetic resonance imaging;
Oligohydramnios
- From:
Chinese Journal of Radiology
2014;48(12):973-976
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the value of MRI on fetal autosomal recessive polycystic kidney disease (ARPKD).Methods Sixteen pregnant women,aged from 28 to 38 years (average 30 years) and with gestation age from 22 to 36 weeks (average 25 weeks) underwent MR scanning with a 1.5 T MR unit within 24 to 48 hours after ultrasound examinations.The imaging sequences included steady-state free-precession (SSFP) sequence,single-shot turbo spin echo (SSTSE) sequence and T1-weighted fast imaging sequence.Prenatal US and MR imaging findings were compared with autopsy or pathological results.Results A total of 16 cases of ARPKD showed bilateral markedly enlarged kidneys and diffuse high signal small cysts in renal medulla on SSTSE sequence.Among the 16 cases,11 cases were with oligohydramnios,1 1 cases were with pulmonary hypoplasia,and 6 cases were with hepatic fibrosis.Eleven cases of pulmonary hypoplasia and 6 cases of hepatic fibrosis were all missed by US.For the diagnosis of the renal anomalies,US missed one case.MRI diagnosis was correct in all these cases.Conclusions MRI shows great advantages on the diagnosis of fetal ARPKD,and it is not affected by the amount of amniotic fluid.It can be used to evaluate kidney and lung abnormalities accurately.
