Kumar C Anand, Jagat Reddy R C, Gupta Siddarth, Laller Sanjeev
Department of Oral Medicine and Radiology, Kanti Devi Dental College and Hospital, Mathura, Uttar Pradesh, India.
Ann Saudi Med. 2011 Jul-Aug;31(4):428-30. doi: 10.4103/0256-4947.76407.
Neurofibromatosis is a genetically-inherited disorder of the nervous system that primarily affects the development and growth of neural (nerve) cell tissues and also causes cafe-au-lait spots on the skin, dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. The two major classifications are NF-1, a generalized form, is the commonest and affects peripheral nerve tissues and NF-2, a rare central form, affects the central nervous system. An unusual finding of oral hamartomas may occur as part of NF-1 and here we presented one such rare case of oral hamartomas in a patient with Von-Recklinghausen's disease.
神经纤维瘤病是一种遗传性神经系统疾病，主要影响神经（神经）细胞组织的发育和生长，还会导致皮肤上出现牛奶咖啡斑、皮肤、神经系统、骨骼、内分泌器官和血管的发育异常。主要分为两种类型：NF-1，一种全身性形式，最为常见，影响周围神经组织；NF-2，一种罕见的中枢性形式，影响中枢神经系统。口腔错构瘤的异常表现可能是NF-1的一部分，在此我们报告了1例患有冯·雷克林豪森病患者出现口腔错构瘤的罕见病例。
