Dysgerminoma in a child with ataxia-telangiectasia

被引：15

作者：

Koksal, Yavuz ^{[1
]}

Caliskan, Umran ^{[2
]}

Ucar, Canan ^{[2
]}

Yurtcu, Muslim ^{[3
]}

Artac, Hasibe ^{[4
]}

Ilerisoy-Yakut, Zeynep ^{[5
]}

Reisli, Ismail ^{[4
]}

机构：

[1] Selcuk Univ, Fac Med, Dept Pediat Oncol, Konya, Turkey

[2] Selcuk Univ, Fac Med, Dept Pediat Hematol, Konya, Turkey

[3] Selcuk Univ, Fac Med, Dept Pediat Surg, Konya, Turkey

[4] Selcuk Univ, Fac Med, Dept Pediat Immunol & Allergy, Konya, Turkey

[5] Fatih Univ, Fac Med, Dept Radiol, Ankara, Turkey

来源：

PEDIATRIC HEMATOLOGY AND ONCOLOGY | 2007年 / 24卷 / 5-8期

关键词：

ataxia; -; telangiectasia; childhood; dysgerminoma; CA125; beta-human chorionic gonadotropin; treatment;

D O I：

10.1080/08880010701451434

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

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.

引用

页码：431 / 436

页数：6

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