Malignant germ cell tumours in two siblings

Med Pediatr Oncol. 1993;21(4):299-300. doi: 10.1002/mpo.2950210413.

Abstract

Familial germ cell tumours are well recognised in kinship with gonadal dysgenesis, but their occurrence in siblings with normal chromosomes is rare. We report two sisters who presented within a 4 month period with malignant ovarian germ cell tumours; one a dysgerminoma and the other a mixed tumour with marked choriocarcinomatous elements. Both children had a normal female constitutional karyotype and normal phenotype.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bleomycin / administration & dosage
  • Carboplatin / administration & dosage
  • Chemotherapy, Adjuvant
  • Child
  • Choriocarcinoma / drug therapy
  • Choriocarcinoma / genetics
  • Choriocarcinoma / surgery
  • Dysgerminoma / drug therapy
  • Dysgerminoma / genetics*
  • Dysgerminoma / surgery
  • Etoposide / administration & dosage
  • Female
  • Humans
  • Neoplasms, Germ Cell and Embryonal / drug therapy
  • Neoplasms, Germ Cell and Embryonal / genetics*
  • Neoplasms, Germ Cell and Embryonal / surgery
  • Nuclear Family
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / surgery

Substances

  • Bleomycin
  • Etoposide
  • Carboplatin

Supplementary concepts

  • JEB protocol