Fay Alex J, King Allison A, Shimony Joshua S, Crow Yanick J, Brunstrom-Hernandez Jan E
Department of Neurology, University of California, San Francisco, San Francisco, California.
Program in Occupational Therapy, Division of Hematology-Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.
Pediatr Neurol. 2017 Jun;71:56-59. doi: 10.1016/j.pediatrneurol.2017.03.008. Epub 2017 Mar 23.
Leukoencephalopathy with calcifications and cysts is a rare, autosomal recessive cerebral microangiopathy that causes progressive white matter disease, calcifications, and cysts within the brain. It is typically associated with slowly progressive psychomotor regression, seizures, and movement disorders. Although leukoencephalopathy with calcifications and cysts affects only the central nervous system, it demonstrates remarkable neuropathologic and radiologic overlap with Coats plus, a disorder of small vessels of the brain, eyes, gastrointestinal tract, and bone. Coats disease without extraocular involvement, a genetically distinct disorder from Coats plus, is characterized by retinal telangiectasias and exudative retinopathy, accompanied by neovascularization. Inhibition of vascular endothelial growth factor (VEGF) signaling with the monoclonal anti-VEGF antibody bevacizumab can improve retinal edema and exudates in Coats disease. Given these observations, we reasoned that VEGF inhibition might also be effective in treating leukoencephalopathy with calcifications and cysts and Coats plus, neither of which has any known therapy.
We treated an 18-year-old man with leukoencephalopathy with calcifications and cysts using biweekly infusions of the VEGF inhibitor bevacizumab for more than one year and performed clinical examinations and brain imaging at three month intervals.
After treatment for more than one year, the patient showed improved bradykinesia and range of motion, and brain magnetic resonance imaging demonstrated a marked reduction in cyst volume and white matter lesions.
Further studies in a cohort of patients are warranted to investigate the efficacy of VEGF inhibition as a treatment for leukoencephalopathy with calcifications and cysts.
伴有钙化和囊肿的白质脑病是一种罕见的常染色体隐性遗传性脑微血管病,可导致进行性白质疾病、脑内钙化和囊肿。它通常与缓慢进展的精神运动发育迟缓、癫痫发作和运动障碍有关。虽然伴有钙化和囊肿的白质脑病仅影响中枢神经系统,但它在神经病理学和放射学上与科茨加综合征有显著重叠,科茨加综合征是一种累及脑、眼、胃肠道和骨骼的小血管疾病。无眼外受累的科茨病是一种与科茨加综合征基因不同的疾病,其特征为视网膜毛细血管扩张和渗出性视网膜病变,并伴有新生血管形成。用单克隆抗血管内皮生长因子(VEGF)抗体贝伐单抗抑制VEGF信号传导可改善科茨病的视网膜水肿和渗出。基于这些观察结果,我们推测VEGF抑制可能对伴有钙化和囊肿的白质脑病以及科茨加综合征也有效,这两种疾病目前均无已知的治疗方法。
我们对一名患有伴有钙化和囊肿的白质脑病的18岁男性患者,每两周静脉输注VEGF抑制剂贝伐单抗,治疗时间超过一年,并每隔三个月进行一次临床检查和脑部成像。
经过一年多的治疗,患者的运动迟缓得到改善,活动范围增加,脑磁共振成像显示囊肿体积和白质病变明显减少。
有必要对一组患者进行进一步研究,以探讨VEGF抑制作为伴有钙化和囊肿的白质脑病治疗方法的疗效。