Familial small cell carcinoma of the ovary

Pediatr Blood Cancer. 2009 Dec 15;53(7):1334-6. doi: 10.1002/pbc.22184.

Abstract

Ovarian tumors have a low incidence in childhood, accounting for 1% of malignancies within the ages of 0-17 years. Small cell carcinoma of the ovary is a rare histology and historically has a poor prognosis. We report a case of an 11-year-old female diagnosed with small cell carcinoma of the ovary and hypercalcemia (SCCOHT). There was a strong family history of the disease, a reduction in the age of onset in the proband, and the absence of BRCA mutations. This case suggests the phenomenon of genetic anticipation in an ovarian cancer.

Publication types

  • Case Reports

MeSH terms

  • Abdominal Pain / etiology
  • Adult
  • Age of Onset
  • Anticipation, Genetic*
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bleomycin / administration & dosage
  • Carcinoma, Small Cell / blood
  • Carcinoma, Small Cell / drug therapy
  • Carcinoma, Small Cell / epidemiology
  • Carcinoma, Small Cell / genetics*
  • Carcinoma, Small Cell / radiotherapy
  • Carcinoma, Small Cell / surgery
  • Chemotherapy, Adjuvant
  • Child
  • Cisplatin / administration & dosage
  • Combined Modality Therapy
  • Diseases in Twins
  • Etoposide / administration & dosage
  • Family Health
  • Female
  • Hormone Replacement Therapy
  • Humans
  • Hypercalcemia / etiology
  • Incidence
  • Menopause, Premature
  • Ovarian Neoplasms / blood
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / epidemiology
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / radiotherapy
  • Ovarian Neoplasms / surgery
  • Ovariectomy
  • Pedigree
  • Radiotherapy, Adjuvant
  • Remission Induction

Substances

  • Bleomycin
  • Etoposide
  • Cisplatin

Supplementary concepts

  • BEP protocol