A 13-year patient journey of infant giant clival chordoma: case report and literature review

被引：1
|
作者：
Apps, J. [1 ,2 ,4 ]
Gagen, R. [2 ,3 ]
Neumann, E. [1 ,2 ]
Solanki, G. [4 ]
English, M. [1 ,2 ]
机构：
[1] Birmingham Womens & Childrens NHS Fdn Trust, Dept Oncol, Birmingham, W Midlands, England
[2] Birmingham Womens & Childrens NHS Fdn Trust, Dept Neurosurg, Birmingham, W Midlands, England
[3] Birmingham Womens & Childrens NHS Fdn Trust, Radiol Dept, Birmingham, W Midlands, England
[4] Univ Birmingham, Canc Res Clin Trials Unit, Birmingham, W Midlands, England
来源：
CHILDS NERVOUS SYSTEM | 2023年 / 39卷 / 04期
关键词：
Infant clival chordoma; Imatinib; mTOR; CHILDREN;
D O I：
10.1007/s00381-022-05749-4
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (TS) Kombogiorgas (Childs Nerv Syst 22(10):1369-1374, 2006). In this report, we provide an update on this patient's journey through a range of therapeutic options and summarize an update of the literature, since 2006, for this patient group.
引用
收藏
页码：1077 / 1081
页数：5
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