Streeten B W, Robinson M R, Wallace R, Jones D B
Department of Ophthalmology, State University of New York Health Science Center, Syracuse 13210.
Arch Ophthalmol. 1987 Dec;105(12):1693-7. doi: 10.1001/archopht.1987.01060120091033.
The ultrastructure of the glomerular basement membrane in Alport's syndrome is well known and characteristic of this disease, but the anterior lenticonus that frequently occurs in this syndrome has not been similarly studied. An anterior lens capsule from a 30-year-old patient with lenticonus who had Alport's syndrome was obtained at capsulectomy and found to be one third the normal thickness centrally and to be more fibrillar than usual. There were large numbers of partial capsular dehiscences containing fibrillar material and vacuoles. Cellular debris and more recent ruptures of lens epithelial cell membranes underlaid the breaks. The anterior capsule is clearly fragile in this disease, forming the basis for the progressive lenticonus and anterior polar cataract. These abnormalities correlate well with a defect in the type IV collagen molecule, as has been recently reported in Alport's syndrome.
阿尔波特综合征肾小球基底膜的超微结构是该疾病所特有的且广为人知,但该综合征中常见的圆锥形晶状体前突尚未得到类似研究。一名患有圆锥形晶状体且患有阿尔波特综合征的30岁患者在晶状体囊切除术时获取的前晶状体囊,发现其中心厚度仅为正常厚度的三分之一,且比正常情况更具纤维性。存在大量含有纤维状物质和空泡的部分囊膜裂开。细胞碎片以及晶状体上皮细胞膜更近的破裂位于这些裂口之下。在这种疾病中,前囊膜明显脆弱,这构成了进行性圆锥形晶状体和前极性白内障的基础。正如最近在阿尔波特综合征中所报道的,这些异常与IV型胶原分子的缺陷密切相关。