两名兄弟姐妹中脉络膜骨瘤的非典型暴发性病程。
An atypical fulminant course of choroidal osteoma in two siblings.
作者信息
Eting E, Savir H
机构信息
Department of Ophthalmology, Golda Medical Center, Hasharon Hospital, Petach-Tikva, Israel.
出版信息
Am J Ophthalmol. 1992 Jan 15;113(1):52-5. doi: 10.1016/s0002-9394(14)75753-8.
We studied two cases of bilateral choroidal osteoma in an otherwise healthy 5-year-old boy and his only sibling, a 7-year-old sister. Both children were known to have normal fundus appearances at younger ages. The tumor showed slow growth in all four eyes, but severe visual acuity loss developed in three eyes because of neovascular complications that could not be effectively treated by photocoagulation. Secondary retinal cysts developed in three eyes.
我们研究了一名5岁健康男孩及其唯一的兄弟姐妹（一名7岁女孩）双侧脉络膜骨瘤的两个病例。已知这两个孩子在较小时眼底外观正常。肿瘤在所有四只眼中均生长缓慢，但由于光凝无法有效治疗的新生血管并发症，三只眼出现了严重的视力丧失。三只眼出现了继发性视网膜囊肿。
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