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Case 62 - Nephroblastomatosis

from Section 6 - Urinary imaging

Published online by Cambridge University Press:  05 June 2014

Gregory Cheeney
Affiliation:
Stanford University
Rakhee Gawande
Affiliation:
Stanford University
Beverley Newman
Affiliation:
Lucile Packard Children's Hospital, Stanford University
Heike E. Daldrup-Link
Affiliation:
Lucile Packard Children's Hospital, 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 four-year-old boy presented with large palpable flank masses bilaterally. An ultrasound (not shown) revealed bilaterally enlarged kidneys with homogeneous low echogenicity, resembling renal cortex. A contrast-enhanced CT was performed which showed a thick rim of non-enhancing, homogeneous soft tissue, surrounding centrally enhancing renal parenchyma (Fig. 62.1). Bilateral homogeneous non-enhancing soft tissue surrounding the renal parenchyma is a typical finding in diffuse bilateral nephroblastomatosis. Another patient with a similar presentation is shown in Figure 62.2. In this case, axial contrast-enhanced CT images demonstrate multiple lenticular, uniform, non-enhancing lesions in the renal cortex (Fig. 62.2), consistent with the more common multifocal type of nephroblastomatosis. On CT, focal nephroblastomatosis appears as low attenuation, subcapsular, or intraparenchymal lesions with poor enhancement relative to that of adjacent normal renal parenchyma. On MRI, focal nephroblastomatosis demonstrates low to intermediate signal intensity foci on both T1- and T2-weighted sequences. Both types of nephroblastomatosis typically resemble the normal renal cortex with regard to their echogenicity on ultrasound, and density and signal intensity on unenhanced CT and MRI. After contrast media injection, however, the lesions typically show no or only minimal enhancement. Contrast administration is helpful in differentiating nephroblastomatosis from Wilms’ tumor. The latter is typically inhomogeneous and enhances after contrast media administration.

Type
Chapter
Information
Pearls and Pitfalls in Pediatric Imaging
Variants and Other Difficult Diagnoses
, pp. 260 - 263
Publisher: Cambridge University Press
Print publication year: 2014

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References

Cormier, PJ, Donaldson, JS, Gonzalez-Crussi, F. Nephroblastomatosis: missed diagnosis. Radiology 1988;169(3):737–8.CrossRefGoogle ScholarPubMed
Lowe, LH, Isuani, BH, Heller, RM. Pediatric renal masses: Wilms tumor and beyond. Radiographics 2000;20(6):1585–603.CrossRefGoogle ScholarPubMed
Lowe, LH, Taboada, EM. Pediatric kidney cancer. In: Baert, AL, Sartor, LK, eds. Imaging of Kidney Cancer. Berlin: Springer, 2006; 351–70.CrossRefGoogle Scholar
Rohrschneider, WK, Weirich, A, Rieden, K, et al. US, CT and MR imaging characteristics of nephroblastomatosis. Pediatr Radiol 1998;28(6):435–43.CrossRefGoogle Scholar

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