Fois A, Vascotto M, Di Bartolo R M, Di Marco V
Institute of Clinical Pediatrics, University of Siena, Italy.
Childs Nerv Syst. 1994 Sep;10(7):450-4. doi: 10.1007/BF00303610.
Among 783 patients referred to our institute with different types of seizures as presenting symptom, systematic evaluation of antigliadin and antiendomysial antibodies in the serum has identified nine in whom jejunal biopsy has subsequently confirmed the diagnosis of celiac disease (CD). In three of them brain imaging showed the presence of calcified areas in the occipital region. They had complex partial seizures (CPS), associated in two with transient episodes of blindness. In another patient with CPS and generalized tonic-clonic seizures (GTCS) progressive multifocal cerebral calcifications were noted. In the other six patients with CPS and/or GTCS cerebral calcifications were absent. Symptoms of CD in all these cases were either not previously taken into account, or they were very mild or completely absent. In a group of 36 patients with clinically manifest CD, regular follow-up, and good compliance with the dietary regimen, no clinical seizures were reported. The pathogenetic mechanism and the relationship between epilepsy and an early diagnosis and treatment of celiac disease are discussed.
在我院以不同类型癫痫发作为主要症状前来就诊的783例患者中,通过对血清中抗麦醇溶蛋白抗体和抗肌内膜抗体进行系统评估,发现9例患者经空肠活检随后确诊为乳糜泻(CD)。其中3例患者的脑部影像学检查显示枕叶存在钙化区域。他们患有复杂部分性发作(CPS),其中2例伴有短暂性失明发作。另1例患有CPS和全身强直-阵挛发作(GTCS)的患者发现有进行性多灶性脑钙化。其他6例患有CPS和/或GTCS的患者未出现脑钙化。所有这些病例中,CD的症状要么之前未被考虑到,要么非常轻微或完全没有。在一组36例临床表现为CD的患者中,进行定期随访且患者对饮食方案依从性良好,未报告有临床癫痫发作。本文讨论了发病机制以及癫痫与乳糜泻早期诊断和治疗之间的关系。