双侧自发性晶状体脱位,视网膜血管炎和早衰样改变。

M Sharir, L Ragenbogen
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引用次数: 0

摘要

本文报告一位70岁男性患者,表现为早衰样综合征,包括早衰(按病史)、弥漫性消瘦、皮肤萎缩、弥散性骨骼骨质疏松症(记录至少25年),主要表现为脊柱和指骨关节,身材矮小,鼻尖,声音尖细。成熟型晶状体白内障自发性双侧脱位进入玻璃体并伴有双侧视网膜血管炎,以静脉充血、扭曲和闭塞为特征,据我们所知,尚未见一人同时具有上述所有特征的病例报告,因此,鉴别诊断也将讨论。
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Bilateral spontaneous dislocated lenses, retinal vasculitis and progeria-like changes.

Findings are reported for a 70-year-old man with a progeria-like syndrome consisting of premature aging (per history), diffuse wasting, skin atrophy, disseminated skeletal osteoporosis (documented for at least 25 years), especially in the vertebral column and metacarpal joints with short stature, beaked nose and high-pitched voice, The ocular findings include: spontaneous bilateral dislocation of spherophakic mature cataracts into the vitreous together with bilateral retinal vasculitis, characterized by venous congestion, tortuosity and occlusion, To the best of our knowledge, there is no case report with all the above features in one person, Hence, the differential diagnosis will also be discussed.

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