Baloh R W, Vinters H V
Department of Neurology, UCLA School of Medicine, USA.
Arch Neurol. 1995 Oct;52(10):975-81. doi: 10.1001/archneur.1995.00540340067014.
To identify the cause of subcortical white matter lesions seen on magnetic resonance imaging in older patients with progressive deterioration of gait and balance.
Postmortem examination of three patients with objective impairment of gait and balance thought to be due to subcortical white matter lesions identified on magnetic resonance imaging. Brain sections were stained with routine methods and for glial fibrillary acid protein using an immunoperoxidase technique.
Part of a prospective study of gait and balance problems in older people. None had a history of hypertension or discrete strokelike episodes.
Other than a few small infarcts in the basal ganglia and internal capsule in the patient with the mildest gait disorder, there were no gross or microscopic features on routine examination post mortem to explain the white matter hyperintensities on magnetic resonance imaging or the progressive gait deterioration. By contrast, immunohistochemical staining with anti-glial fibrillary acid protein showed prominent astrocytosis T2-weighted high-intensity signal areas on magnetic resonance imaging.
The astrocytes presumably swell as they take up extravasated protein at the site of a breakdown in the blood-brain barrier, and the increased water content per unit volume increases the magnetic resonance imaging proton signal. We hypothesized that the astrocytes may have been initially activated by small infarcts or subclinical ischemia, but the process then became self-perpetuating, ultimately involving most of the white matter and producing the severe gait disorder.
确定在磁共振成像上出现皮质下白质病变的老年患者步态和平衡逐渐恶化的原因。
对三名步态和平衡存在客观损害的患者进行尸检,这些损害被认为是由磁共振成像上发现的皮质下白质病变所致。脑切片采用常规方法染色,并使用免疫过氧化物酶技术对胶质纤维酸性蛋白进行染色。
一项关于老年人步态和平衡问题的前瞻性研究的一部分。所有患者均无高血压病史或明确的类中风发作史。
除步态障碍最轻的患者基底节和内囊有少量小梗死灶外,尸检常规检查未发现肉眼或显微镜下特征可解释磁共振成像上的白质高信号或步态进行性恶化。相比之下,用抗胶质纤维酸性蛋白进行免疫组化染色显示,磁共振成像上T2加权高信号区域有明显的星形细胞增生。
星形胶质细胞可能在血脑屏障破坏部位摄取外渗蛋白时肿胀,单位体积内增加的含水量增加了磁共振成像质子信号。我们推测,星形胶质细胞最初可能由小梗死灶或亚临床缺血激活,但该过程随后变得自我持续,最终累及大部分白质并导致严重的步态障碍。