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Dysgerminoma in a child with ataxia-telangiectasia.
- Source :
-
Pediatric hematology and oncology [Pediatr Hematol Oncol] 2007 Sep; Vol. 24 (6), pp. 431-6. - Publication Year :
- 2007
-
Abstract
- Ataxia-telangiectasia is an autosomal recessive disease characterized by progressive cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, high incidence of cancer, and increased sensitivity to ionizing radiation. The authors report a case of dysgerminoma in a child with high alpha-fetoprotein, CA125 and beta-human chorionic gonadotropin, who has been followed-up for ataxia-telangiectasia for 2 years.
- Subjects :
- Antineoplastic Combined Chemotherapy Protocols adverse effects
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Ataxia Telangiectasia blood
Ataxia Telangiectasia therapy
Biomarkers, Tumor blood
Bleomycin administration & dosage
Bleomycin adverse effects
CA-125 Antigen blood
Carboplatin administration & dosage
Child
Chorionic Gonadotropin, beta Subunit, Human blood
Dysgerminoma drug therapy
Dysgerminoma surgery
Etoposide administration & dosage
Female
Follow-Up Studies
Genetic Predisposition to Disease
Humans
Immunoglobulins, Intravenous therapeutic use
Neoplasm Proteins blood
Ovarian Neoplasms drug therapy
Ovarian Neoplasms surgery
Ovariectomy
Respiration Disorders chemically induced
alpha-Fetoproteins analysis
Ataxia Telangiectasia complications
Dysgerminoma etiology
Ovarian Neoplasms etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1521-0669
- Volume :
- 24
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Pediatric hematology and oncology
- Publication Type :
- Academic Journal
- Accession number :
- 17710660
- Full Text :
- https://doi.org/10.1080/08880010701451434