These ultrasound images reveal unilateral hydronephrosis of the left fetal kidney. The renal pelvis and calyces appear dilated with thinning of the renal parenchyma in the affected kidney. The commonest cause of such hydronephrosis is PUJ (Pelvi-ureteral junctional) obstruction, usually functional. The left ureter does not appear to be dilated. For cases of dilatation of the renal pelvis, it is labelled as abnormal if the RPD (renal pelvic A-P diameter) is more than 10mm (after 20 weeks gestational age). If less than 20 weeks, more than 4mm. is abnormal. These ultrasound images are courtesy of Dr. Arun Mahajan, Delhi, India.'); //]]>
Sonography of the fetal abdomen in this 2nd trimester fetus reveals- 1) bilateral grossly enlarged fetal kidneys, almost filling the entire abdomen 2) markedly hyperechoic fetal kidneys with minute anechoic areas within them. 3) oligohydramnios 4) poorly distended urinary bladder. This ultrasound image is diagnostic of fetal autosomal recessive polycystic kidney disease (ARPKD). This image was taken by Dr. Durr-e-Sabih, Pakistan, using a Toshiba Nemio-30 color doppler machine.'); //]]>
These ultrasound images (another case) also show grossly enlarged, echogenic fetal kidneys with minute cystic lesions (1 to 2 mm.) within them. The cystic lesions in this case, as well as the previous case show a typical rosette like pattern that is typical of autosomal recessive polycystic kidney disease. These ultrasound images are courtesy of Dr. Jaydeep Gandhi, Mumbai India. The machine used is a Nemio 30 from Toshiba.
Reference: E-medicine article on ARPKD
http://www.jultrasoundmed.org/cgi/reprint/22/1/105.pdf (free article and images).
Solitary cyst of fetal kidney. This fetus of 30 weeks gestational age underwent sonography of the fetal abdomen. Ultrasound images show a small anechoic rounded lesion of the lower pole. The walls of the lesion are smooth and the contents appear to be clear fluid with no septae or tissue. There is also evidence of posterior acoustic enhancement. These ultrasound findings (images) are diagnostic of simple renal cyst (left kidney). Solitary renal cysts in fetus are a rare occurrence and may be of little clinical importance, but need to followed by serial scans for changes in characteristics or size. The lower right shows a 3-D ultrasound image of the fetal renal cyst. All images are courtesy of Ravi Kadasne, MD, UAE.
Sonography of this 3rd trimester fetus shows 1) keyhole urinary bladder (an overdistended bladder with the dilated prostatic urethra forming a keyhole like appearance). 2) hydronephrotic kidneys (bilateral) with thinning of the renal cortex. These ultrasound images suggest fetal lower urinary tract obstruction, probably a posterior urethral valve. Some degree of pelvi-ureteric junction obstruction may also be present. Images by Joe Antony, MD, India. Images taken using a GE- Logic 3 ultrasound system .
A rare case of ureterocele detected sonographically in 3rd trimester fetus Sonography of the fetal urinary bladder, shows a sac like structure (arrow) in the region of the distal end of the fetal left ureter. This ultrasound image suggests fetal ureterocele. Ureterocele is often seen in adults, but very rarely in a fetus. It is caused by defect during in embryogenesis of the fetal ureter. Ultrasound image is courtesy of Dr. Latha Natarajan, India.
This 20 Week Old Fetus shows enlarged kidneys on both sides with severe oligohydramnios. In addition, the kidneys appear echogenic with multiple cysts, of varying sizes, within the Fetal renal tissue. Colour Doppler Study shows the renal arteries on both sides but little or no vascularity within the Fetal renal tissue. These Findings are consistent with a diagnosis of multicystic kidney disease, in this case, bilateral in nature. Multicystic dysplastic kidney disease is usually unilateral, however in this case it is bilateral. Bilateral multicystic dysplastic kidneys are more common in female foetuses. Multicystic Disease of the Kidneys is usually the result of chronic obstruction in the early stages of Fetal development. Bilateral multicystic dysplastic kidneys in foetuses is invariably fatal. The Main Differential Diagnosis in multicystic dysplastic kidneys is autosomal recessive polycystic kidney disease of the fetus. However, in multicystic kidneys, as in this case, the Fetal kidneys appear poorly defined in outline. In autosomal recessive polycystic kidney disease of the fetus, the kidneys are markedly enlarged with well defined margins. Besides, in autosomal recessive polycystic kidney disease, the cysts are small in size and are of uniform size and arranged in a rosette pattern. In multicystic dysplastic kidney, as in this case, the cysts are of larger size and of various sizes.