La Mantia L, Pollo B, Savoiardo M, Costa A, Eoli M, Allegranza A, Boiardi A, Cestari C
Department of Clinical Neurology, Istituto Nazionale Neurologica C. Besta, Milan, Italy.
Clin Neurol Neurosurg. 1998 Sep;100(3):209-15. doi: 10.1016/s0303-8467(98)00029-8.
A woman with ophthalmic migraine was found to have bilateral cerebellar and cerebral calcifications. She progressively developed severe intracranial hypertension, with swelling of the brain and downward transtentorial and tonsillar herniation. Because steroid treatment was ineffective, the right occipital pole was resected. Histological study demonstrated meningo-cortical calcifying angiomatosis. Within 2 months, brain swelling and papilledema disappeared. Subtle signs of malabsorption led to the hypothesis of celiac disease, confirmed by jejunal biopsy. Similar cerebral histological findings have been reported in the brain of two young patients affected by epilepsy and celiac disease. The association between cerebral calcifications and celiac disease is peculiar; the pathogenetic relationship is unknown.
一名患有眼型偏头痛的女性被发现双侧小脑和大脑钙化。她逐渐发展为严重的颅内高压,伴有脑肿胀以及经天幕向下和扁桃体疝形成。由于类固醇治疗无效,切除了右侧枕极。组织学研究显示为脑膜-皮质钙化性血管瘤病。两个月内,脑肿胀和视乳头水肿消失。轻微的吸收不良迹象引发了乳糜泻的假说,空肠活检证实了这一假说。在两名患有癫痫和乳糜泻的年轻患者的大脑中也报告了类似的脑组织学发现。脑钙化与乳糜泻之间的关联很特殊;发病机制尚不清楚。