Ohno Kousaku
Department of Child Neurology, Tottori University Hospital.
Nihon Rinsho. 2010 Jan;68(1):131-5.
Neurofibromatosis type 1(NF1) is an autosomal dominant disorder with variable expression. The complications are age specific. Serious complication during early childhood is rare but optic glioma, brain tumors or leukemia may appear. Learning difficulties and attention deficit hyperactive disorders occur in as many as 60% of patients during school age. Overall, intelligence in neurofibromatosis is normal and mental retardation occurs in 6-7%. Managements for learning difficulties and attention deficit hyperactive disorders are especially important for quality of life in these patients. Skin neurofibromas or subcutaneous plexiform neurofibromas appear during childhood and may cause pain or spinal cord involvement. Malignant peripheral nerve sheath tumors that arise from plexiform neurifibromas are a particularly devastating complication during middle age.
1型神经纤维瘤病(NF1)是一种具有可变表达的常染色体显性疾病。其并发症具有年龄特异性。幼儿期的严重并发症很少见,但可能会出现视神经胶质瘤、脑肿瘤或白血病。多达60%的患者在学龄期会出现学习困难和注意力缺陷多动障碍。总体而言,神经纤维瘤病患者的智力正常,6 - 7%的患者会出现智力迟钝。针对学习困难和注意力缺陷多动障碍的管理对这些患者的生活质量尤为重要。皮肤神经纤维瘤或皮下丛状神经纤维瘤在儿童期出现,可能会引起疼痛或脊髓受累。由丛状神经纤维瘤引发的恶性外周神经鞘瘤是中年时期一种特别具有破坏性的并发症。