Weiss A H, Kousseff B G, Ross E A, Longbottom J
Department of Ophthalmology, University of South Florida Medical Center, Tampa 33612.
Arch Ophthalmol. 1989 Nov;107(11):1619-24. doi: 10.1001/archopht.1989.01070020697031.
Forty patients were diagnosed as having complex microphthalmos on the basis of a malformed globe with a total axial length measurement at least 2 SDs below the mean for age-similar controls. Three had anterior segment dysgenesis; 4, congenital lens abnormalities; 14, chorioretinal colobomas; 12, persistent hyperplastic primary vitreous; 4, retinal dysplasia; and 3, complex malformations due to ipsilateral facial malformations. Measurements of total axial length indicated that complex microphthalmos was congenital and that postnatal growth of the malformed eye was similar to that of normal eyes. In most patients the anterior segment length was normal, while in all patients the posterior segment length was at least 2 SDs below the mean. Corneal diameter correlated significantly with total axial length (r2 = .57) and decreased linearly as total axial length decreased. In most patients in whom measurements were obtained, the lens and corneal power were increased, thereby compensating for decreased total axial length. We propose that inadequate production of secondary vitreous is the cause of the microphthalmos, given that the posterior segment was disproportionately reduced in size and the secondary vitreous is its predominant component. Evidence that each of the various ocular malformations can influence the production of secondary vitreous is presented.
40例患者根据眼球畸形被诊断为复杂性小眼症,其总眼轴长度测量值至少比年龄匹配的对照组均值低2个标准差。3例有眼前节发育异常;4例有先天性晶状体异常;14例有脉络膜视网膜缺损;12例有永存原始玻璃体增生症;4例有视网膜发育异常;3例因同侧面部畸形导致复杂畸形。总眼轴长度测量表明复杂性小眼症是先天性的,畸形眼的出生后生长与正常眼相似。大多数患者眼前节长度正常,而所有患者眼后节长度至少比均值低2个标准差。角膜直径与总眼轴长度显著相关(r2 = 0.57),并随着总眼轴长度的减少而呈线性下降。在大多数进行测量的患者中,晶状体和角膜屈光力增加,从而补偿总眼轴长度的减少。鉴于眼后节大小不成比例地减小且继发性玻璃体是其主要成分,我们提出继发性玻璃体生成不足是小眼症的病因。文中还给出了各种眼部畸形均可影响继发性玻璃体生成的证据。