Department of Pediatrics, American University of Beirut, Medical Center, Beirut, Lebanon.
Epileptic Disord. 2009 Dec;11(4):293-300. doi: 10.1684/epd.2009.0280. Epub 2009 Dec 23.
Pyridoxine-dependent epilepsy (PDE) is a rare disease, of which the EEG manifestations are only partially characterised. We report our observations of EEG recordings in four patients with PDE.
EEG tracings from four patients fulfilling the clinical criteria for PDE were reviewed. Relative to the time of treatment with pyridoxine, EEG recordings were available before treatment in two patients (at ages four and 10 months), immediately after treatment in two patients and during long-term follow-up with treatment in all four patients.
Pre-pyridoxine interictal EEG findings included: diffuse slowing, bilateral independent multifocal epileptiform discharges, generalized bursts of polyspike slow waves and focal or generalized sharp waves. In addition, the EEG was often asymmetrical and included: generalized semi-rhythmic sharp and slow waves, a burst suppression pattern and continuous generalized spike and slow waves. In one patient, who was followed subsequently, a decrease in multifocal spikes and sharp waves and permanent cessation of clinical seizures, within 10 minutes of concurrent reduction of spikes in the pre-existing generalized spike slow wave pattern, was observed immediately after pyridoxine treatment. However, despite the clinical response in this patient we observed persistent generalized burst suppression for four days, and fluctuation of the EEG with diffuse slowing on day four and transient exacerbation of discharges with continuous spike slow waves on day 22. This was followed by intermittent sharp waves at eight and 20 months, mild slowing at 31 months and normal EEG at 43 months. Long-term EEG findings in the other three patients receiving pyridoxine ranged between normal and intermittent multifocal sharp waves.
Our data confirm previous observations and provide the following new findings: (1) the presence of burst suppression pattern after cessation of seizures can occur for up to five days after initiation of pyridoxine and should not exclude the diagnosis of PDE, (2) possible fluctuation and even transient worsening of electrographic discharges were observed for up to three weeks after initiation of pyridoxine and (3) the abnormal EEG can persist for up to 43 months before normalizing (range 1-43 months) and in other cases in which it continues to be abnormal it may still improve after increasing the dose of pyridoxine.
吡哆醇依赖性癫痫(PDE)是一种罕见疾病,其脑电图表现仅部分特征化。我们报告了对四名符合 PDE 临床标准的患者的脑电图记录观察结果。
回顾了四名满足 PDE 临床标准的患者的脑电图记录。相对于使用吡哆醇治疗的时间,两名患者在治疗前(4 月龄和 10 月龄)有脑电图记录,两名患者在治疗后立即有脑电图记录,所有四名患者均在长期随访中接受治疗。
吡哆醇治疗前的发作间期脑电图发现包括:弥漫性减慢,双侧独立多灶性癫痫样放电,广泛性多棘慢波爆发和局灶或广泛性尖波。此外,脑电图通常不对称,包括:广泛的半节律性尖波和慢波,爆发抑制模式以及连续的广泛棘慢波。在一名随后接受随访的患者中,在接受吡哆醇治疗后立即观察到,在原有广泛棘慢波模式中的棘波减少的同时,多灶性棘波和尖波减少,并且临床发作停止,而在接受治疗后的四天内观察到持续的广泛爆发抑制,在第四天出现脑电图弥漫性减慢的波动,以及在第 22 天出现连续棘慢波放电的短暂恶化。之后在第 8 个月和第 20 个月出现间歇性尖波,第 31 个月轻度减慢,第 43 个月脑电图正常。其他三名接受吡哆醇治疗的患者的长期脑电图发现介于正常和间歇性多灶性尖波之间。
我们的数据证实了之前的观察结果,并提供了以下新发现:(1)在开始使用吡哆醇后,即使在癫痫发作停止后,仍可能出现爆发抑制模式,持续时间长达五天,不应排除 PDE 的诊断,(2)在开始使用吡哆醇后长达三周内观察到电描记法放电的波动,甚至短暂恶化,(3)异常脑电图在恢复正常前可持续长达 43 个月(范围 1-43 个月),在其他情况下,如果继续异常,增加吡哆醇剂量后仍可能改善。