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Pediatr Blood Cancer ; 53(7): 1334-6, 2009 Dec 15.
Article in English | MEDLINE | ID: mdl-19621450

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.


Subject(s)
Anticipation, Genetic , Carcinoma, Small Cell/genetics , Ovarian Neoplasms/genetics , Abdominal Pain/etiology , Adult , Age of Onset , 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/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/radiotherapy , Ovarian Neoplasms/surgery , Ovariectomy , Pedigree , Radiotherapy, Adjuvant , Remission Induction
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