Cystic partially differentiated nephroblastoma (CPDN) is a rare multicystic renal tumor along the spectrum of cystic nephroma and cystic Wilms' tumor. There have only been two previously reported cases of bilateral CPDN in the literature. We present here a case of bilateral CPDN vs cystic Wilms' tumor treated with neoadjuvant and adjuvant chemotherapy in addition to a bilateral partial nephrectomy. We also review the relevant literature regarding CPDN in an effort to aid in diagnosis and management of these rare cystic renal tumors.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.urology.2016.01.018 | DOI Listing |
Pediatr Dev Pathol
December 2024
Department of Pathology, Sidra Medicine, Doha, Qatar.
Cystic partially differentiated nephroblastoma (CPDN) is a rare pediatric renal tumor composed of multiple cystic spaces divided by septa containing immature nephrogenic elements. The presence of expansile solid areas in the septa of such a lesion indicates an alternative diagnosis of Wilms tumor (WT). We present a unique case of CPDN associated with grossly visible polypoid proliferations, which histologically correspond to botryoid growth of intralobar nephrogenic rests.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Department of Pathology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON K1H 8L1, Canada.
FP Essent
August 2024
Urology Division, Department of Surgery, Womack Army Medical Center.
Kidney cysts and tumors often are identified during imaging for unrelated issues. Kidney cysts can be attributable to heritable polycystic kidney diseases. These cysts are rare in children.
View Article and Find Full Text PDFPediatr Blood Cancer
October 2024
Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Background: Concomitant Wilms tumor (WT) and autosomal dominant polycystic kidney disease (ADPKD) is exceedingly rare, presenting a diagnostic and technical challenge to pediatric surgical oncologists. The simultaneous workup and management of these disease processes are incompletely described.
Procedure: We performed a retrospective analysis of patients treated at our institution with concomitant diagnoses of WT and ADPKD.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!