Wilms Tumor in Child With Trisomy 18 and Horseshoe Kidney

Author:

Chen Elizabeth1,Hackney Lisa2,VanHeyst Kristen2,Miyasaka Eiichi A.3

Affiliation:

1. Case Western Reserve University School of Medicine

2. Department of Pediatrics, Division of Pediatric Hematology Oncology

3. Division of Pediatric Surgery, Rainbow Babies and Children’s Hospital at University Hospitals Cleveland Medical Center, Cleveland, OH

Abstract

Trisomy 18 is associated with several congenital malformations, including horseshoe kidney. It can be full, partial, or mosaic, and mosaicism is often associated with lesser severity and longer life expectancy, placing patients at greater risk of developing neoplasms or malignancies. One common tumor among children with Trisomy 18 is Wilms tumor, which is also associated with renal congenital abnormalities such as horseshoe kidney. We present a case describing the occurrence of these three characteristics: development of Wilms tumor in a patient with Trisomy 18 and a horseshoe kidney and discuss treatment with regards to these conditions.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference37 articles.

1. Congenital anomalies associated with trisomy 18 or trisomy 13: a registry-based study in 16 European countries, 2000-2011;Springett;Am J Med Genet A,2015

2. Anatomy of trisomy 18;Roberts;Clin Anat,2016

3. The trisomy 18 syndrome;Cereda;Orphanet J Rare Dis,2012

4. Age distribution of Wilms’ tumor: report from the National Wilms’ Tumor Study;Breslow;Cancer Res,1988

5. CT findings of the main pathological conditions associated with horseshoe kidneys;Schiappacasse;Br J Radiol,2015

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