A Case Report of Atypical Teratoid/ Rhabdoid Tumour in a 9-Year-Old Girl

被引：0
作者：
Chan, Kin Hup [1 ]
Haspani, Mohammed Saffari Mohammed [2 ]
Tan, Yew Chin [1 ]
Kassim, Fauziah [3 ]
机构：
[1] Univ Sains Malaysia, Sch Med Sci, Dept Neurosci, Kubang Kerian 16150, Kelantan, Malaysia
[2] Hosp Kuala Lumpur, Dept Neurosurg, Kuala Lumpur 50586, Malaysia
[3] Hosp Kuala Lumpur, Dept Pathol, Kuala Lumpur 50586, Malaysia
来源：
MALAYSIAN JOURNAL OF MEDICAL SCIENCES | 2011年 / 18卷 / 03期
关键词：
central nervous system neoplasms; child; oncology; recurrence; rhabdoid tumour; teratoma;
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
Primary central nervous system atypical rhabdoid/teratoid tumour (ATRT) is a rare and highly malignant tumour that tends to occur in infancy and early childhood. The majority of tumours (approximately two-third) arise in the posterior fossa. The optimal treatment for ATRT remains unclear. Options of treatment include surgery, radiotherapy, and chemotherapy. Each of their role is still not clearly defined until now. The prognosis of the disease is generally unfavourable. This is a case report of ATRT in an atypical site in a 9-year-old girl.
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页码：82 / 86
页数：5
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