Tai Patricia, Dubey Arbind, Salim Muhammad, Vu Khanh, Koul Rashmi
1Allan Blair Cancer Center,Regina,Saskatchewan.
2CancerCare Manitoba,Winnipeg,Manitoba.
Can J Neurol Sci. 2015 Nov;42(6):410-3. doi: 10.1017/cjn.2015.285. Epub 2015 Aug 27.
When patients with cranial glioblastoma develop weakness, a rare differential diagnosis is spinal metastases.
Chart and literature reviews were performed.
The reported patient had delayed onset spinal drop metastasis that was only detected by magnetic resonance imaging (MRI). A 48-year-old patient had supratentorial glioblastoma, treated with radiotherapy (RT) and concurrent temozolomide followed by six cycles of adjuvant temozolomide. Four years after completion of all treatments (62 months from initial presentation), he developed low backache and weakness in both legs. Positron emission tomography/computed tomography scans demonstrated intracranial recurrence only. Spinal drop metastases were detected only by MRI scan. Local spinal RT 40 Gy in 20 fractions with concurrent and maintenance temozolomide were given. Because of disease progression after nine cycles of temozolomide, systemic therapy was changed to bevacizumab, which greatly improved his symptoms for 4 months before deterioration of mental status. He is still alive with disease at 22 months after diagnosis of spinal metastases (84 months from initial glioblastoma diagnosis).
MRI is the diagnostic imaging of choice for spinal metastases. This illustrative case of delayed-onset spinal metastases shows unusual slow progression. Local RT, temozolomide, and targeted therapy may improve survival. This illustrative case is the first report of bevacizumab as a second-line therapy in drop metastasis of glioblastoma.
当颅部胶质母细胞瘤患者出现肌无力时,一种罕见的鉴别诊断是脊髓转移。
进行了病历和文献回顾。
报告的患者出现延迟性脊髓播散转移,仅通过磁共振成像(MRI)检测到。一名48岁患者患有幕上胶质母细胞瘤,接受了放疗(RT)和同步替莫唑胺治疗,随后进行了六个周期的辅助替莫唑胺治疗。在所有治疗完成四年后(距首次就诊62个月),他出现了下背部疼痛和双腿无力。正电子发射断层扫描/计算机断层扫描仅显示颅内复发。仅通过MRI扫描检测到脊髓播散转移。给予局部脊髓放疗40 Gy,分用20次,同步和维持使用替莫唑胺。由于在九个周期的替莫唑胺治疗后疾病进展,全身治疗改为贝伐单抗,在精神状态恶化前,他的症状得到了4个月的显著改善。在诊断脊髓转移后22个月(距最初诊断胶质母细胞瘤84个月),他仍带瘤生存。
MRI是脊髓转移的诊断性影像学检查方法。这个延迟性脊髓转移的病例显示了不寻常的缓慢进展。局部放疗、替莫唑胺和靶向治疗可能会提高生存率。这个病例是贝伐单抗作为胶质母细胞瘤播散转移二线治疗的首例报告。