Pediatric intradural extramedullary synovial sarcoma: Case report

被引:14
作者
Greene, Stephanie [1 ]
Hawkins, Douglas S.
Rutledge, Joe C.
Tsuchiya, Karen D.
Douglas, James
Ellenbogen, Richard G.
Avellino, Anthony M.
机构
[1] Univ Washington, Childrens Hosp & Reg Med Ctr, Sch Med, Dept Neurol Surg, Seattle, WA 98195 USA
[2] Univ Washington, Childrens Hosp & Reg Med Ctr, Sch Med, Dept Pediat,Div Hematol & Oncol, Seattle, WA 98195 USA
[3] Univ Washington, Childrens Hosp & Reg Med Ctr, Sch Med, Dept Lab Med, Seattle, WA 98195 USA
[4] Univ Washington, Childrens Hosp & Reg Med Ctr, Sch Med, Dept Radiat Oncol, Seattle, WA 98195 USA
关键词
extramedullary; intradural; pediatric; sarcoma; spinal; synovial;
D O I
10.1227/01.NEU.0000245619.24603.96
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: The diagnosis of intradural synovial sarcoma has not been previously published. This report provides a summary of the literature on this tumor and on tumors arising in this location, as well as a description of this patient's clinical course. CLINICAL PRESENTATION: An 11-year-old girl presented with back pain and radiculopathy. A magnetic resonance imaging scan of the spine revealed a spinal intradural, extramedullary mass at L2-L4 and four additional nodules of enhancement. INTERVENTION: The mass was nearly totally resected. Radiation and chemotherapy were administered. Intracranial metastases became evident during treatment. The patient died of the disease 14 months after diagnosis. CONCLUSION: The rapid progression of leptomeningeal metastasis despite maximal treatment demonstrates the aggressive nature of the tumor and the need for further study. Copyright © by the Congress of Neurological Surgeons.
引用
收藏
页码:1339 / 1339
页数:1
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