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J Pediatr Hematol Oncol. 2012 Oct;34(7):548-51.

Development of anaplastic Wilms tumor and subsequent relapse in a child with diaphanospondylodysostosis.

Author information

  • 1Department of Pediatrics, Division of Pediatric Hematology-Oncology, University of California, San Francisco School of Medicine, San Francisco, CA, USA. tasians@email.chop.edu

Abstract

Diaphanospondylodysostosis (DSD) is a rare skeletal dysplasia syndrome resulting from disordered mesenchymal differentiation. Children with DSD generally die in utero or during the first month of life from severe thoracic insufficiency syndrome. An association of DSD with nephroblastomatosis has been observed, but the natural history of such nephroblastomatosis remains poorly characterized due to the rarity of the underlying condition. We describe a patient with DSD who developed bilateral hyperplastic nephroblastomatosis that ultimately evolved into therapy-resistant anaplastic Wilms tumor (nephroblastoma).

PMID:
22469945
[PubMed - indexed for MEDLINE]
PMCID:
PMC3394881
Free PMC Article

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