常染色体隐性多囊肾病的产前诊断。一份病例报告。

K Mine, S Suzuki, S Watanabe, R Sawa, Y Yoneyama, H Asakura, T Araki
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引用次数: 2

摘要

我们报告一例常染色体隐性多囊肾病的诊断在妊娠28周超声检查和磁共振成像(MRI)。超声检查胎儿肾脏对称增大,回声高,MRI t2加权图像显示高信号强度。两项检查均未发现囊性病变。此外,胎儿肾动脉脉搏指数正常。这些结果提示常染色体隐性多囊肾病肾实质含水量高,有小囊肿,血流正常。
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Prenatal diagnosis of autosomal recessive polycystic kidney disease. A case report.

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.

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