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Ocular fundus in neurofibromatosis type 2.

机译:2型神经纤维瘤病的眼底

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摘要

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.
机译:自从该疾病被鉴定为独特的临床实体以来,已有数种眼部发现与2型神经纤维瘤病(NF 2)相关。首先报道了青少年白内障,其次是色素上皮和视网膜错构瘤。在最近的一份报告中,九名患者中有七名描述了视网膜前膜。此外,基于较早发表的报告,已经提出了NF 2和视神经胶质瘤之间的联系。检查了六名确诊为NF 2的患者。 4例患者(12眼中的6例)具有视网膜前膜,其中1例患有视神经胶质瘤。另外,追踪了1例NF 2患者的视神经胶质瘤。结论是在NF 2中视网膜前膜很常见,而视神经胶质瘤是NF 2的一种罕见但特定的征象。有此病风险的患者应仔细检查眼底。

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