Brain atypical teratoid rhabdoid tumor in an adult with long-term survival: Case report and review of literature

被引：2

作者：

Moujahed, Rim ^{[1
,2
]}

Ghedira, Khalil ^{[3
]}

Zehani, Alia ^{[2
,4
,5
]}

Charfi, Slim ^{[6
,7
]}

Nagi, Sonia ^{[2
,8
,9
]}

机构：

[1] Abderrahmen Mami Hosp, Dept Radiotherapy, Ariana, Tunisia

[2] Univ Tunis El Manar, Fac Med Tunis, Ariana, Tunisia

[3] Natl Inst Neurol, Dept Neurosurg, Tunis 1007, Tunisia

[4] Univ Tunis El Manar, Fac Med, Tunis, Tunisia

[5] Rabta Hosp, Dept Pathol, Tunis, Tunisia

[6] Habib Bourguiba Hosp, Dept Pathol, Sfax, Tunisia

[7] Univ Sfax, Fac Med Sfax, Sfax, Tunisia

[8] Natl Inst Neurol, Dept Neuroradiol, Tunis, Tunisia

[9] Univ Tunis El Manar, Fac Med Tunis, Tunis, Tunisia

来源：

JOURNAL OF CANCER RESEARCH AND THERAPEUTICS | 2020年 / 16卷

关键词：

Adult; atypical teratoid; rhabdoid tumor; brain; survival; TERATOID/RHABDOID TUMOR; EPIDEMIOLOGY; RADIOTHERAPY; FEATURES;

D O I：

10.4103/jcrt.JCRT_554_18

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Atypical teratoid/rhabdoid tumor (AT/RT) represents a rare malignant embryonic tumor of infant and early childhood. Its prognosis remains dismal despite aggressive multimodal treatment. We report the case of a 24-year-old male who was diagnosed with left parietal AT/RT after total resection and who is still in good health and recurrence free 4 years after surgery and adjuvant chemotherapy and radiotherapy.

引用

页码：S243 / S245

页数：3

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