Department of Neurology, Sydney Children's Hospital, Sydney, NSW, Australia.
Dev Med Child Neurol. 2013 Jan;55(1):90-3. doi: 10.1111/j.1469-8749.2012.04369.x. Epub 2012 Jul 31.
A 4-year-old boy presented with occipital seizures but normal initial neuroimaging and proved refractory to antiepileptic medications. On repeat neuroimaging after 1 year, he had developed bi-occipital calcification and was then found to have positive coeliac serology. He was diagnosed with coeliac disease, epilepsy, and cerebral calcifications (CEC) and became seizure free after starting the gluten-free diet. Positive antibody binding to neurons and glia was demonstrated on indirect immunofluorescence. High levels of immunoglobulin-A directed against transglutaminase isoenzyme 6 (TG6) were found in the patient's serum. The positive response to the diet, TG6 antibodies, and neuronal antibody binding suggest that CEC might be autoimmune in nature, as in other extra-intestinal manifestations of gluten-related diseases, such as gluten ataxia.
一位 4 岁男孩以枕叶癫痫发作为首发表现,初始神经影像学检查未见异常,且对抗癫痫药物治疗反应不佳。1 年后复查神经影像学检查时,他出现双侧枕叶钙化,随后发现乳糜泻相关血清学阳性。他被诊断为乳糜泻、癫痫和脑钙化(CEC),并在开始无麸质饮食后癫痫无发作。间接免疫荧光显示针对神经元和神经胶质的抗体呈阳性结合。患者血清中针对转谷氨酰胺酶同工酶 6(TG6)的免疫球蛋白 A 水平升高。对饮食、TG6 抗体和神经元抗体结合的阳性反应提示 CEC 可能具有自身免疫性质,就像其他与麸质相关疾病的肠外表现一样,如麸质共济失调。