Ocular fundus in neurofibromatosis type 2.
Ocular fundus in neurofibromatosis type 2.
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2 型神经纤维瘤病的眼底。
DOI：
10.1136/bjo.77.10.646
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发表时间：
1993
影响因子：
4.1
通讯作者：
G. M. Yaargil
中科院分区：
文献类型：
--
作者：
K. Landau;Gazi M Ya§;G. M. Yaargil
自从神经纤维瘤病2型（NF 2）被确认为一种独特的临床疾病以来，一些眼部表现与NF 2相关。青少年白内障首先被报道，其次是色素上皮和视网膜错构瘤。在最近的一份报告中，9名患者中有7名描述了视网膜前膜。此外，NF 2和视盘胶质瘤之间的关联已被建议基于早期发表的报告。对6例确诊为NF 2的患者进行了检查。4例患者（12只眼中的6只眼）有视网膜前膜，1例有视盘胶质瘤。此外，还追踪了一例NF 2患者的视盘胶质瘤.结论是视网膜前膜是常见的NF 2，视盘胶质瘤是一种罕见的，但具体的迹象NF 2。有患此病风险的患者应仔细检查眼底。
Several ocular findings have been associated with neurofibromatosis type 2 (NF 2) since the identification of this disease as a distinct clinical entity. Juvenile cataracts were reported first, followed by combined pigment epithelial and retinal hamartomas. In a recent report, epiretinal membranes were described in seven of nine patients. Moreover, an association between NF 2 and optic disc gliomas has been suggested based on earlier published reports. Six patients with a confirmed diagnosis of NF 2 were examined. Four patients (six of 12 eyes) had epiretinal membranes and one had an optic disc glioma. In addition, one case of an optic disc glioma in a patient with NF 2 was tracked. It is concluded that epiretinal membranes are frequent in NF 2, and that optic disc glioma is a rare but specific sign of NF 2. Patients at risk for development of this disease should undergo careful examination of the ocular fundus.
影响因子：
56.9
作者：
BARKER, D;WRIGHT, E;SKOLNICK, M
通讯作者：
SKOLNICK, M