Rhabdomyosarcoma, osteosarcoma, and adrenocortical carcinoma in a child with a germline p53 mutation

Pediatr Blood Cancer. 2004 Nov;43(6):683-6. doi: 10.1002/pbc.20142.

Abstract

A child with an unusual association of cancers is described. The patient first presented with a rhabdomyosarcoma of the right scapular muscle, and was successfully treated with chemotherapy. Six years after diagnosis of the first malignancy, the child presented with two synchronous malignancies: osteosarcoma of the jaw and adrenocortical carcinoma. Genetic mutation analysis was performed and revealed a germline p53 mutation of CGT > CAT at codon 273. The family history was negative for any other cancer consistent with the Li-Fraumeni syndrome. This case highlights the need for close surveillance of patients with p53 mutation for malignancy and describes the occurrence of two malignancies synchronously.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Cortex Neoplasms / complications
  • Adrenal Cortex Neoplasms / drug therapy
  • Adrenal Cortex Neoplasms / genetics*
  • Adrenal Cortex Neoplasms / pathology
  • Child
  • Follow-Up Studies
  • Germ-Line Mutation / genetics*
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Osteosarcoma / complications
  • Osteosarcoma / drug therapy
  • Osteosarcoma / genetics*
  • Osteosarcoma / pathology
  • Rhabdomyosarcoma / complications
  • Rhabdomyosarcoma / drug therapy
  • Rhabdomyosarcoma / genetics*
  • Rhabdomyosarcoma / pathology
  • Tomography Scanners, X-Ray Computed
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • Tumor Suppressor Protein p53