Polster T, Hoppe M, Ebner A
Klinik Mara I, Epilepsiezentrum Bethel, Maraweg 21, D-33617 Bielefeld, Germany.
J Neurol Neurosurg Psychiatry. 2001 Apr;70(4):459-63. doi: 10.1136/jnnp.70.4.459.
Focal lesions limited to the splenium of the corpus callosum (SCC) are rare and little is known about their aetiology. Three patients were examined for presurgical evaluation in epilepsy with a transient lesion in the SCC and a pathophysiological hypothesis is presented.
Three patients were identified with a circumscribed lesion in the centre of the corpus callosum. Follow up MRI was performed, the medical records examined retrospectively, and the literature reviewed.
The patients showed identical lesions in the SCC with reduced T1 and increased T2 signal intensity and an unaffected marginal hemline of a few mm. Patients were asymptomatic and control MRIs showed complete normalisation within 2 months. Patients had been treated with antiepileptic drugs (AEDs) without signs of toxicity. In all patients AEDs were rapidly reduced for diagnostic purposes, but only one had psychomotor seizures, 5 days before imaging.
A transient lesion in the SCC has so far only been described in 13 patients with epilepsy and has been interpreted either as reversible demyelination due to AED toxicity or transient oedema after secondary generalised seizures. The data confirm neither of these hypotheses. A transient lesion in the SCC seems to be a non-specific end point of different disease processes leading to a vasogenic oedema. This suggests, in these patients, a multifactorial pathology triggered by transient effects of AEDs on arginine vasopressin and its function in fluid balance systems in a condition of vitamin deficiency. The complete and rapid reversibility in all cases without specific intervention is emphasised and any invasive diagnostic or therapeutic approach is discouraged.
局限于胼胝体压部(SCC)的局灶性病变较为罕见,其病因鲜为人知。本文对3例患有SCC短暂性病变的癫痫患者进行术前评估,并提出一种病理生理假说。
确定3例患者胼胝体中部有一局限性病变。进行了随访磁共振成像(MRI),回顾性检查病历,并查阅了文献。
患者的SCC出现相同病变,T1信号降低,T2信号增强,边缘有几毫米未受影响。患者无症状,对照MRI显示2个月内完全恢复正常。患者曾接受抗癫痫药物(AEDs)治疗,无中毒迹象。为诊断目的,所有患者的AEDs均迅速减量,但只有1例在成像前5天出现精神运动性发作。
迄今为止,仅在13例癫痫患者中描述过SCC的短暂性病变,其被解释为要么是由于AED毒性导致的可逆性脱髓鞘,要么是继发性全身性癫痫发作后的短暂性水肿。这些数据均未证实上述假说。SCC的短暂性病变似乎是不同疾病过程导致血管源性水肿的非特异性终点。这表明,在这些患者中,在维生素缺乏的情况下,AEDs对精氨酸血管加压素及其在液体平衡系统中的功能产生短暂影响,从而引发多因素病理改变。强调了所有病例在无特殊干预情况下的完全且快速可逆性,不鼓励采取任何侵入性诊断或治疗方法。