Scuderi G, Papale A, Nucci C, Cerulli L
University of Rome, Tor Vergata Department of Surgery, Italy.
Int Ophthalmol. 1995;19(6):375-8. doi: 10.1007/BF00130858.
Retinal involvement has been documented in a number of patients with pigment dispersion syndrome, which also appears to be associated with a higher than normal risk of retinal detachment. We studied 24 patients with this syndrome to determine the prevalence of lattice degeneration and other retinal disorders associated with a predisposition to detachment. Lattice degeneration was found in 8 of 24 patients examined, with a prevalence that is significantly higher than that reported for normal subjects. Four eyes presented areas of retinoschisis and only one displayed a rhegmatogenous detachment. A father and son (both myopes) were found to have similar lattice lesions in the same retinal quadrants. These findings suggest that pigment dispersion syndrome may be associated with developmental anomalies that are not restricted to the anterior chamber but involve other portions of the bulb as well.
许多色素性分散综合征患者已被证实存在视网膜受累情况,该综合征似乎还与高于正常水平的视网膜脱离风险相关。我们研究了24例患有此综合征的患者,以确定与视网膜脱离易感性相关的格子样变性及其他视网膜疾病的患病率。在接受检查的24例患者中,有8例发现存在格子样变性,其患病率显著高于正常受试者报告的患病率。4只眼出现了视网膜劈裂区域,仅有1只眼表现为孔源性视网膜脱离。发现一名父亲和儿子(均为近视)在相同的视网膜象限有相似的格子样病变。这些发现表明,色素性分散综合征可能与发育异常有关,这种异常不仅局限于前房,还累及眼球的其他部分。