Dysgerminoma in a child with ataxia-telangiectasia

Koksal Y., Caliskan U., Ucar C., Yurtcu M., Artac H., Ilerisoy-Yakut Z., ...Daha Fazla

PEDIATRIC HEMATOLOGY AND ONCOLOGY, cilt.24, sa.5-8, ss.431-436, 2007 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 24 Sayı: 5-8
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1080/08880010701451434
  • Dergi Adı: PEDIATRIC HEMATOLOGY AND ONCOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.431-436
  • Ondokuz Mayıs Üniversitesi Adresli: Hayır

Özet

Alaxia - 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-letangiectasia for 2 years.