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Malignant rhabdoid tumor of the extremity.

作者信息

Kent A L, Mahoney D H, Gresik M V, Steuber C P, Fernbach D J

出版信息

Cancer. 1987 Sep 1;60(5):1056-9. doi: 10.1002/1097-0142(19870901)60:5<1056::aid-cncr2820600521>3.0.co;2-q.

DOI:10.1002/1097-0142(19870901)60:5<1056::aid-cncr2820600521>3.0.co;2-q
PMID:3607724
Abstract

Two cases of malignant rhabdoid tumor (MRT) involving the sciatic nerve are described. Despite the close affiliation of the tumor with neural tissue, staining characteristics in these patients do not suggest a neural origin of MRT. Survival in patients with renal and extrarenal MRT has been poor. Our patients were treated with an aggressive chemotherapy program using cisplatin, Adriamycin (doxorubicin), vincristine, cyclophosphamide, actinomycin D, and DTIC. One child died of progressive disease; the other is well 35 months after diagnosis.

摘要

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引用本文的文献

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Sarcoma. 2013;2013:315170. doi: 10.1155/2013/315170. Epub 2013 Feb 3.
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Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood.婴幼儿及儿童中枢神经系统非典型畸胎样/横纹肌样肿瘤
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