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伴冯·雷克林霍增氏病的口腔错构瘤

Oral hamartomas with von Recklinghausen disease.

作者信息

Kumar C Anand, Jagat Reddy R C, Gupta Siddarth, Laller Sanjeev

机构信息

Department of Oral Medicine and Radiology, Kanti Devi Dental College and Hospital, Mathura, Uttar Pradesh, India.

出版信息

Ann Saudi Med. 2011 Jul-Aug;31(4):428-30. doi: 10.4103/0256-4947.76407.

Abstract

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.

摘要

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。

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