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Autosomal recessive polycystic kidney disease

Case contributed by Dr Bahman Rasuli


34 weeks gestational age fetus with abnormality seen in routine obstetric ultrasound. Severe oligohydramnios (AFI<2cm). AC: 40 weeks. BPD, HC and FL:34 weeks

Patient Data

Age: 30 years
Gender: Female

Both kidneys are markedly enlarged and show increased parenchymal echo-pattern with decreased cortico-medullary differentiation. No stones or masses. No pelvicalyceal dilatation bilaterally.

The right kidney averages  8.5 x 5.6cm 

The left kidney averages 8.4 x 4.7 cm 

Diffuse bilateral renal tiny parenchymal cysts with increased parenchymal echo pattern, suggestive of autosomal recessive polycystic kidney disease.


Case Discussion

The findings are those of autosomal recessive polycystic kidney disease (ARPKD).

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Case information

rID: 81270
Published: 21st Aug 2020
Last edited: 21st Aug 2020
System: Obstetrics
Inclusion in quiz mode: Included
Institution: Jame Jam Imaging Center

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