Melson G L, Shackelford G D, Cole B R, McClennan B L
J Clin Ultrasound. 1985 Feb;13(2):113-9. doi: 10.1002/jcu.1870130206.
We evaluated nine patients, age 1 day to 17 years, having infantile polycystic kidney disease (IPKD). Using modern scanners with 5-MHz transducers we have observed two previously unemphasized sonographic (US) findings, a peripheral zone of normally echogenic cortex (five patients), and mild caliectasis (two patients). Our data suggest that IPKD is a more heterogeneous condition clinically and sonographically than generally appreciated and that presence of a thick normally echogenic renal cortex is a good predictor of concurrent normal renal function and prolonged survival.
我们评估了9例年龄从1天至17岁的患有婴儿型多囊肾病(IPKD)的患者。使用配备5兆赫换能器的现代扫描仪,我们观察到了两个以前未被强调的超声(US)表现:正常回声的皮质外周带(5例患者)和轻度肾盂扩张(2例患者)。我们的数据表明,IPKD在临床和超声检查方面比一般认识到的更为异质性,并且正常回声的肾皮质增厚是并发正常肾功能和延长生存期的良好预测指标。