Eichler April F, Batchelor Tracy T, Henson John W
Pappas Center for Neuro-Oncology, Boston, MA 02114, USA.
Neuro Oncol. 2007 Jul;9(3):373-7. doi: 10.1215/15228517-2007-015. Epub 2007 May 23.
Methotrexate (MTX) is a widely used chemotherapeutic agent that can cause acute, subacute, and chronic neurological complications. Subacute MTX neurotoxicity is manifest by abrupt onset of focal cerebral dysfunction occurring days to weeks after MTX administration, usually in children. We describe the neuroimaging features of an adult patient with primary CNS lymphoma who presented with transient aphasia and right hemiparesis 12 days after receiving intravenous high-dose MTX (8 g/m2) chemotherapy. Imaging within 1 h of symptom onset showed bilateral symmetrical restricted diffusion involving white matter of the cerebral hemispheres. CT angiogram and dynamic susceptibility MRI showed no evidence of vasospasm or perfusion defect. MRI five days later showed near-complete resolution of the abnormalities. MRI 3(1/2) months later showed normal diffusion but new hyperintense T2-weighted signal changes in the subcortical white matter corresponding to previous areas of restricted diffusion. The absence of vascular or perfusion abnormalities suggests that transient cytotoxic edema in white matter may explain the syndrome of subacute MTX neurotoxicity.
甲氨蝶呤(MTX)是一种广泛使用的化疗药物,可引起急性、亚急性和慢性神经并发症。亚急性MTX神经毒性表现为在MTX给药数天至数周后突然出现局灶性脑功能障碍,通常发生在儿童身上。我们描述了一名原发性中枢神经系统淋巴瘤成年患者的神经影像学特征,该患者在接受静脉高剂量MTX(8 g/m²)化疗12天后出现短暂性失语和右侧偏瘫。症状发作后1小时内的影像学检查显示双侧对称的扩散受限,累及大脑半球白质。CT血管造影和动态磁敏感MRI显示无血管痉挛或灌注缺陷的证据。五天后的MRI显示异常几乎完全消退。3个半月后的MRI显示扩散正常,但皮质下白质出现新的T2加权高信号变化,对应于先前扩散受限的区域。血管或灌注异常的缺失表明白质中的短暂细胞毒性水肿可能解释亚急性MTX神经毒性综合征。