Stroke Unit, Department of Internal Medicine, Aging and Nephrological Diseases, University of Bologna, 40138 Bologna, Italy.
World J Gastroenterol. 2012 Jul 14;18(26):3472-6. doi: 10.3748/wjg.v18.i26.3472.
Celiac disease (CD) is frequently associated with neurological disorders, but very few reports concern the association with ischemic stroke. A 26-year-old woman affected by CD with secondary amenorrhea, carrier of a homozygous 5,10-methylenetetrahydrofolate reductase mutation with hyperhomocysteinemia, was affected by two occipital ischemic strokes within a period of 5 mo. At the time of the second stroke, while she was being treated with folic acid, acetylsalicylic acid and a gluten-free diet, she had left hemianopsia, left hemiparesthesias, and gait imbalance. Brain magnetic resonance imaging showed a subacute right occipital ischemic lesion, which was extended to the dorsal region of the right thalamus and the ipsilateral thalamo-capsular junction. Antitransglutaminase and deamidated gliadin peptide antibodies were no longer present, while antinuclear antibodies, antineuronal antibodies and immune circulating complexes were only slightly elevated. Since the patient was taking folic acid, her homocysteine levels were almost normal and apparently not sufficient alone to explain the clinical event. A conventional cerebral angiography showed no signs of vasculitis. Finally, rare causes of occipital stroke in young patients, such as Fabry's disease and mitochondrial myopathy, encephalomyopathy, lactic acidosis and stroke-like symptoms, were also excluded by appropriate tests. Thus, the most probable cause for the recurrent strokes in this young woman remained CD, although the mechanisms involved are still unknown. The two main hypotheses concern malabsorption (with consequent deficiency of vitamins known to exert neurotrophic and neuroprotective effects) and immune-mediated mechanisms. CD should be kept in mind in the differential diagnosis of ischemic stroke in young patients.
乳糜泻(CD)常与神经系统疾病相关,但很少有报道涉及与缺血性中风的关联。一名 26 岁的女性患有 CD 伴继发闭经,是同型半胱氨酸血症伴 5,10-亚甲基四氢叶酸还原酶纯合突变的携带者,在 5 个月内发生了两次枕叶缺血性中风。第二次中风时,她正在接受叶酸、乙酰水杨酸和无麸质饮食治疗,出现左侧偏盲、左侧半身感觉异常和步态不平衡。脑磁共振成像显示右侧枕叶亚急性缺血性病变,延伸至右侧丘脑背侧和同侧丘脑-壳核交界处。抗转谷氨酰胺酶和脱酰胺麸质肽抗体不再存在,而抗核抗体、抗神经元抗体和免疫循环复合物仅略有升高。由于患者正在服用叶酸,其同型半胱氨酸水平几乎正常,显然单独服用叶酸不足以解释临床事件。常规脑血管造影未显示血管炎迹象。最后,通过适当的检查排除了年轻患者枕叶中风的罕见原因,如法布里病和线粒体肌病、脑病、乳酸酸中毒和类似中风的症状。因此,尽管涉及的机制尚不清楚,但这位年轻女性反复发作中风的最可能原因仍然是 CD。CD 应在年轻患者缺血性中风的鉴别诊断中予以考虑。