Kumar Sudhir, Kumar Ravi P
Department of Neurological Sciences, Christian Medical College Hospital, Vellore, India.
Indian J Dermatol Venereol Leprol. 2004 Nov-Dec;70(6):361-3.
Neurofibromatosis (NF), one of the commonest phakomatoses, is characterized by varied clinical manifestations. Segmental NF is one of the uncommon subtypes of NF. We report a young adult presenting with asymptomatic skin lesions- neurofibromas and café-au-lait macules- over localized areas of the lower back, affecting more than one segment. None of the family members were found to have features of segmental NF. Segmental NF may be misdiagnosed as a birthmark or remain undiagnosed for long periods of time, as the patients are often asymptomatic. Moreover, the clinical features are highly variable and range from a small area of skin involvement to involvement over the entire half of the body. This variation is explained by the fact that segmental NF is thought to arise from a postzygotic NF1 gene mutation, leading to somatic mosaicism. We have also reviewed the relevant literature on this subject.
神经纤维瘤病(NF)是最常见的错构瘤病之一,其临床表现多样。节段性NF是NF的罕见亚型之一。我们报告了一名年轻成人,其下背部局部区域出现无症状性皮肤病变——神经纤维瘤和咖啡斑,累及多个节段。未发现其家庭成员有节段性NF的特征。节段性NF可能被误诊为胎记,或长时间未被诊断,因为患者通常无症状。此外,其临床特征高度可变,范围从小面积皮肤受累到累及身体的整个半侧。这种变异的原因是节段性NF被认为是由合子后NF1基因突变引起的,导致体细胞镶嵌现象。我们还回顾了关于该主题的相关文献。