Shah A K
Wayne State University School of Medicine, Detroit Medical Center, Michigan, USA.
Clin Neuropharmacol. 1999 Mar-Apr;22(2):67-73. doi: 10.1097/00002826-199903000-00001.
Cyclosporine A (CsA) neurotoxicity is an iatrogenic disease with significant morbidity and occasional mortality. We retrospectively reviewed the cases of CsA neurotoxicity among bone marrow transplant recipients at our institution, and summarized the current literature on the subject. The neurologic presentation is varied and the neurologic manifestations are reversible, even after prolonged toxicity, in most instances. Serum CsA level is useful in evaluation, as the level is high in most instances. However, in a case of suspected neurotoxicity, withdrawal of the drug is the only way of determining presence or absence of such toxicity. The electrophysiologic studies, especially electroencephalogram (EEG), is very sensitive in identifying the problem, but lacks specificity. On the other hand, the neuroimaging studies are helpful in making a diagnosis if they show characteristic findings of hyperintense lesions affecting posterior cerebral regions on T2 weighted magnetic resonance images (MRI) or white matter hypodensities on computed tomographic (CT) scan. These lesions are probably due to breakdown of blood-brain barrier resulting in leakage of fluid in interstitial space. The breakdown could be serious enough to cause microhemorrhages that may coalesce to produce macrohemorrhages.
环孢素A(CsA)神经毒性是一种医源性疾病,具有较高的发病率,偶尔会导致死亡。我们回顾性分析了我院骨髓移植受者中环孢素A神经毒性的病例,并总结了该主题的现有文献。神经系统表现多样,在大多数情况下,即使经过长期毒性作用,神经表现也是可逆的。血清CsA水平有助于评估,因为大多数情况下该水平较高。然而,在疑似神经毒性的病例中,停用药物是确定是否存在此类毒性的唯一方法。电生理研究,尤其是脑电图(EEG),在识别问题方面非常敏感,但缺乏特异性。另一方面,如果神经影像学研究在T2加权磁共振成像(MRI)上显示影响大脑后部区域的高强度病变或在计算机断层扫描(CT)上显示白质低密度的特征性表现,则有助于做出诊断。这些病变可能是由于血脑屏障破坏导致间质空间液体渗漏所致。这种破坏可能严重到足以引起微出血,微出血可能融合形成大出血。