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神经纤维瘤病在国内已有很多报导。本病为常染色体显性遗传,其发病率占新生儿1/2000～1/3000。现将我科收治一例并由病理活检确诊的神经纤维瘤病报告如下。 患儿卢海全,男,13岁,汉族,学生。住院号A34644。因皮肤多处褐色斑及右侧肢体抽搐,于1986年2月15日住院。生后发现颈、上肢、肩部前胸、后背等处有小片状色素斑,初为淡褐色,随着年龄增长色素变深,问时色素斑也渐扩大,色素斑有的皇深褐色,有的呈黑色。皮肤出现皮下结
Neurofibromatosis has been reported in China. The disease is autosomal dominant inheritance, the incidence of neonatal 1/2000 ~ 1/3000. Now we receive a case of pathological biopsy diagnosed neurofibromatosis reported as follows. Children Luhai full, male, 13 years old, Han nationality, students. Hospital number A34644. Due to skin spots and brown spots on the right side of the seizures, February 15, 1986 hospitalization. After birth, neck, upper extremity, shoulder chest, back and other small patches of pigmented spots at the beginning of the light brown, darkening with age, pigment spots also gradually enlarged, pigmented spots some deep Brown, some black. Skin appears subcutaneous knot