Bonioli E V, Bertola A, Di Stefano A, Bellini C
Istituto di Clinica Pediatrica G. Gaslini, Università di Genova, Italy.
Pediatr Neurol. 1997 Jul;17(1):77-9. doi: 10.1016/s0887-8994(97)80672-8.
Sebaceous nevus (SN) syndrome is a neurocutaneous disorder characterized by a distinctive skin lesion in association with epilepsy and mental retardation. In one group of patients, brain lesions may be consequent to vascular abnormalities ("vascular variant"); another group of SN patients presents ipsilateral hemimegalencephaly, gyral anomalies, and facial hemihypertrophy ("neurologic variant" or "SN with hemimegalencephaly"). In the latter group, facial hemihypertrophy does not appear to be a constant feature and was not present in our 2 SN patients with hemimegalencephaly. Considering that about half of the SN patients with hemimegalencephaly described so far do not have facial asymmetry, we suggest the existence of a separate subgroup of SN patients with hemimegalencephaly and without facial hemihypertrophy. In these patients, the only clinical diagnostic clue is a nevus that is barely visible until puberty.
皮脂腺痣(SN)综合征是一种神经皮肤疾病,其特征为独特的皮肤病变,并伴有癫痫和智力障碍。在一组患者中,脑部病变可能由血管异常引起(“血管变异型”);另一组SN患者表现为同侧半侧巨脑症、脑回异常和面部半侧肥大(“神经学变异型”或“伴半侧巨脑症的SN”)。在后一组中,面部半侧肥大似乎并非恒定特征,在我们的2例伴半侧巨脑症的SN患者中未出现。鉴于迄今为止所描述的伴半侧巨脑症的SN患者中约有一半没有面部不对称,我们建议存在一个单独的伴半侧巨脑症且无面部半侧肥大的SN患者亚组。在这些患者中,唯一的临床诊断线索是直到青春期才勉强可见的痣。