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β–HCG Elevation in Wilms Tumor: An Uncommon Presentation
Authors:Aditya Kumar Gupta MD  FNB  FIAP  Amanda Charlton MBBS  FRCPA  Kristina Prelog MBBS  FRANZCR  Stewart J Kellie MBBS  FRACP  MD  MIntPH
Institution:1. Department of Oncology, Children's Cancer Centre, Children's Hospital at Westmead, Sydney, NSW, Australia;2. Department of Histopathology, Children's Hospital at Westmead, Sydney, NSW, Australia;3. Department of Radiology, Children's Hospital at Westmead, Sydney, NSW, Australia;4. Discipline of Child Health, University of Sydney, NSW, Australia
Abstract:Wilms tumor (nephroblastoma) is a readily diagnosed common abdominal tumor in children. Rarely, it may present with factors that may confound the diagnosis. We report a 6‐year‐old female child who presented with a rapidly growing and invasive abdominal mass with the histopathologic features of Wilms tumor associated with an elevated serum beta human chorionic gonadotropin, which has not been previously reported in this condition.
Keywords:β  ‐HCG  nephroblastoma  tumor marker  Wilms tumor
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