Argubright K F, Wicks J D
Am J Perinatol. 1987 Jan;4(1):1-4. doi: 10.1055/s-2007-999726.
Infantile polycystic kidney disease (Potter's Type 1) is an autosomal recessive disorder that affects the kidneys and liver. Use of ultrasound to make the diagnosis prenatally is well documented and, in fact, it is advocated as a screening device for second-trimester identification of potentially affected fetuses. The sonographic appearance is characterized by enlarged hyperechoic kidneys, enlarging fetal abdominal circumference, and oligohydramnios. It is suggested that a ratio of the kidney circumference to the abdominal circumference (KC/AC) be used as method of quantifying renal size and as a potential indicator of early kidney enlargement associated with infantile polycystic kidney disease (IPKD). We report a case of serial ultrasound examination of a pregnancy at risk for IPKD where the in utero diagnosis was not established until the third trimester.
婴儿型多囊肾病(波特1型)是一种常染色体隐性疾病,会影响肾脏和肝脏。超声用于产前诊断已有充分记录,事实上,它被推荐作为孕中期识别潜在患病胎儿的筛查手段。超声表现的特征为肾脏回声增强且增大、胎儿腹围增大以及羊水过少。有人建议将肾周径与腹周径之比(KC/AC)用作量化肾脏大小的方法以及与婴儿型多囊肾病(IPKD)相关的早期肾脏增大的潜在指标。我们报告了一例对有患IPKD风险的妊娠进行系列超声检查的病例,该病例直到孕晚期才做出宫内诊断。