Mine K, Suzuki S, Watanabe S, Sawa R, Yoneyama Y, Asakura H, Araki T
Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan.
Nihon Ika Daigaku Zasshi. 1999 Jun;66(3):188-90. doi: 10.1272/jnms.66.188.
We present a case of autosomal recessive polycystic kidney disease diagnosed at 28 weeks' gestation by ultrasonographic examination and magnetic resonance imaging (MRI). The fetal kidneys were symmetrically enlarged and highly echogenic by ultrasonographic examination and showed high-signal intensity on T2-weighted images by MRI. Cystic lesions were recognized by neither examination. In addition, the pulsatility index of the fetal renal artery was normal. These findings suggest a high water content in the renal parenchyma with tiny cysts and normal blood flow in autosomal recessive polycystic kidney disease.
我们报告一例通过超声检查和磁共振成像(MRI)在妊娠28周时诊断出的常染色体隐性多囊肾病病例。超声检查显示胎儿双肾对称增大且回声增强,MRI的T2加权图像上显示高信号强度。两种检查均未发现囊性病变。此外,胎儿肾动脉的搏动指数正常。这些发现提示常染色体隐性多囊肾病的肾实质含水量高,伴有微小囊肿且血流正常。