Renal rhabdomyosarcoma in a pancake kidney

Urology. 2013 Aug;82(2):458-60. doi: 10.1016/j.urology.2013.03.003. Epub 2013 Apr 29.

Abstract

Renal rhabdomyosarcoma (RMS) is a rare pediatric tumor. Pancake kidneys are unusual anatomic anomalies resulting when both upper and lower poles of the embryonic kidney become fused. We report on a 4-year-old boy who was discovered to have a stage 4, group IV renal embryonal RMS arising from a pancake kidney with metastases to the lung, pelvis, and bone marrow. Treatment included multimodal therapy, consisting of neoadjuvant chemotherapy, complete surgical resection, and adjuvant chemotherapy. He remains in clinical remission 7 months after resection.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bone Marrow Neoplasms / secondary
  • Bone Marrow Neoplasms / therapy
  • Chemotherapy, Adjuvant
  • Child, Preschool
  • Humans
  • Kidney / abnormalities*
  • Kidney Neoplasms / pathology*
  • Kidney Neoplasms / surgery
  • Kidney Neoplasms / therapy*
  • Lung Neoplasms / surgery
  • Lung Neoplasms / therapy
  • Male
  • Neoadjuvant Therapy
  • Pelvic Neoplasms / secondary
  • Pelvic Neoplasms / therapy
  • Rhabdomyosarcoma / secondary*
  • Rhabdomyosarcoma / surgery
  • Rhabdomyosarcoma / therapy*