Kar Sumit, Preetha Krishnan, Yadav Nidhi, Madke Bhushan, Gangane Nitin
Department of Dermatology, Venereology, Leprosy, Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India.
Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):90-2. doi: 10.4103/0972-2327.144281.
Neurofibromatosis type 1 is an autosomal dominant disorder which primarily affects the growth and development of neural cell tissues. It presents as multiple tumor-like growths over the skin that arises from the nerves and is associated with other abnormalities like pigmentation over the skin and bone deformities. Becker's nevus or hairy pigmented epidermal nevus is a benign cutaneous hamartoma which is characterized by hyperpigmented macule with hypertrichosis. It is rarely associated with neurofibromatosis. We report a 22-years-old male with coexistent Becker's nevus and type 1 neurofibromatosis.
1型神经纤维瘤病是一种常染色体显性疾病，主要影响神经细胞组织的生长和发育。它表现为皮肤上出现多个源于神经的肿瘤样生长物，并伴有其他异常，如皮肤色素沉着和骨骼畸形。贝克尔痣或毛发色素沉着性表皮痣是一种良性皮肤错构瘤，其特征为色素沉着斑伴多毛症。它很少与神经纤维瘤病相关。我们报告一例22岁男性同时患有贝克尔痣和1型神经纤维瘤病。
