[遗传性玻璃体变性混浊：10例报告]
[Hereditary vitreous degeneration muddy: report of ten cases].
作者信息
Shen Zhixin, Gao Enfang, Weng Wenqing, Luo Weiling
机构信息
Department of Ophthalmology, Jiaxing Hospital of Traditional Chinese Medicine, Jiaxing 314000, China.
出版信息
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2016 May 25;45(6):636-640. doi: 10.3785/j.issn.1008-9292.2016.11.13.
Hereditary vitreous degeneration muddy is rare in clinic. Here we report ten cases (thirteen eyes) of hereditary vitreous degeneration muddy from two families. All patients presented with vitreous opacity, and the textures appeared tough and tensile. Two cases had concurrent detachment of rhegmatogenous retina. HE staining showed red changeableness, and methyl violet staining appeared purple. All patients received vitrectomy with traditional Chinese medicine treatment, and got satisfactory efficacy.
遗传性玻璃体混浊在临床上较为罕见。在此，我们报告来自两个家族的10例（13只眼）遗传性玻璃体混浊病例。所有患者均表现为玻璃体混浊，质地坚韧且有张力。2例合并孔源性视网膜脱离。苏木精-伊红染色显示呈红色变化，甲基紫染色呈紫色。所有患者均接受了玻璃体切除术及中药治疗，疗效满意。
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