Oh U, Gupta R, Krakauer J W, Khandji A G, Chin S S, Elkind M S V
Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Neurology. 2004 Feb 10;62(3):494-7. doi: 10.1212/01.wnl.0000106951.94624.df.
The authors describe three patients with reversible leukoencephalopathy associated with cerebral amyloid angiopathy (CAA). Rapid progression of neurologic symptoms was followed by dramatic clinical and radiographic improvement. Pathologically, CAA was associated with varying degrees of inflammation ranging from none to transmural granulomatous infiltration. In the appropriate clinical context, the MRI finding of lobar white matter edema with evidence of prior hemosiderin deposition may indicate the presence of a reversible CAA leukoencephalopathy.
作者描述了3例与脑淀粉样血管病(CAA)相关的可逆性白质脑病患者。神经症状迅速进展,随后临床和影像学显著改善。病理上,CAA与不同程度的炎症相关,从无炎症到透壁肉芽肿浸润。在适当的临床背景下,MRI显示脑叶白质水肿并有先前含铁血黄素沉积证据,可能提示存在可逆性CAA白质脑病。