Unusually long survival of an adult patient with atypical teratoid/rhabdoid tumor of the sellar region: A follow-up report

被引：2

作者：

Almalki, Mussa Hussain ^{[1
,2
]}

Altwairgi, Abdullah ^{[3
]}

Orz, Yasser ^{[4
]}

机构：

[1] King Fahad Med City, Obes Endocrine & Metab Ctr, Riyadh, Saudi Arabia

[2] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, King Fahad Med City, Riyadh, Saudi Arabia

[3] King Fahad Med City, Oncol Ctr, Riyadh, Saudi Arabia

[4] King Fahad Med City, Natl Neurosci Inst, Dept Neurosurg, Riyadh, Saudi Arabia

来源：

IBNOSINA JOURNAL OF MEDICINE AND BIOMEDICAL SCIENCES | 2020年 / 12卷 / 01期

关键词：

Adult; atypical teratoid; rhabdoid tumor; central nervous system neoplasm; prognosis; CENTRAL-NERVOUS-SYSTEM; CHILDHOOD; INFANCY;

D O I：

10.4103/ijmbs.ijmbs_88_19

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Atypical teratoid/rhabdoid tumor (AT/RT) is a rare and very aggressive central nervous system neoplasm that is most often seen in infants and young children. The prognosis remains poor, with a median survival time of <1 year. Here, we report a follow-up on a case of AT/RT that originated in the sellar and suprasellar region in a 42-year-old female patient with unusually long survival.

引用

页码：53 / 56

页数：4

共 13 条

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