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Case 77 - Cystic dysplasia of the kidneys

from Section 8 - Fetal imaging

Published online by Cambridge University Press:  05 June 2014

Erika Rubesova
Affiliation:
Stanford University
Heike E. Daldrup-Link
Affiliation:
Lucile Packard Children's Hospital, Stanford University
Beverley Newman
Affiliation:
Lucile Packard Children's Hospital, Stanford University
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Summary

Imaging description

A 16-year-old patient was diagnosed at 22 weeks of gestational age (GA) with a fetus with multicystic dysplastic kidney (MCDK). The contralateral kidney appeared slightly echogenic but otherwise normal on ultrasound (Fig. 77.1a,b). Fetal MRI confirmed large disorganized cortical cysts of different size in the right kidney but also demonstrated the presence of small subcortical cysts in the left kidney (Fig. 77.1c). However, the amount of amniotic fluid remained normal throughout the pregnancy and the patient carried the baby to term. At birth, ultrasound of the kidneys confirmed a right MCDK that got progressively smaller over time (Fig. 77.1d, f), but failed to demonstrate the small subcortical cysts in the left kidney (Fig. 77.1e). A dysplastic appearance of the left kidney with subcortical cysts was only noticed on follow-up ultrasound at the age of 1 year (Fig. 77.1g). The renal function was mildly decreased postnatally.

Importance

Renal cystic dysplasia is usually unilateral and may affect an entire kidney, a segment of a kidney, or a pole of a duplex kidney. Recent studies demonstrate that MCDK and obstructive dysplasia may have a similar pathogenesis, with glomerular cysts being the initial dysplastic event in the kidneys. Early prenatal studies show that MCDK appear as normal kidneys on ultrasound up to 14 weeks of gestational age despite complete obstruction. They are often diagnosed at the routine anatomic scan around 20 weeks of gestational age. Small subcortical cysts in the setting of obstructive dysplasia may appear later in pregnancy or after birth and are often more difficult to diagnose prenatally than MCDK.

Type
Chapter
Information
Pearls and Pitfalls in Pediatric Imaging
Variants and Other Difficult Diagnoses
, pp. 319 - 321
Publisher: Cambridge University Press
Print publication year: 2014

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References

Aslam, M, Watson, AR; Trent & Anglia MCDK Study Group. Unilateral multicystic dysplastic kidney: long-term outcomes. Arch Dis Child 2006;91(10):820–3.CrossRefGoogle ScholarPubMed
Cambio, AJ, Evans, CP, Kurzrock, EA. Non-surgical management of multicystic dysplastic kidney. BJU Int 2008;101(7):804–8.CrossRefGoogle ScholarPubMed
Kuwertz-Broeking, E, Brinkmann, OA, Von Lengerke, HJ, et al. Unilateral multicystic dysplastic kidney: experience in children. BJU Int 2004;93(3):388–92.CrossRef
Nagata, M, Shibata, S, Shu, Y. Pathogenesis of dysplastic kidney associated with urinary tract obstruction in utero. Nephrol Dial Transplant 2002;17(Suppl 9):37–8.CrossRefGoogle ScholarPubMed

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