Mercé E, Korobelnik J-F, Delyfer M-N, Rougier M-B
Service d'ophtalmologie, CHU Dupuytren, 4, avenue Martin-Luther-King, 87000 Limoges, France.
J Fr Ophtalmol. 2012 Oct;35(8):573-9. doi: 10.1016/j.jfo.2011.12.007. Epub 2012 Jun 12.
Alport syndrome is a progressive inherited glomerulonephritis leading to renal failure, hearing loss and ocular changes.
To report the seventh case of giant macular hole in a patient with Alport syndrome, review the literature, and propose a pathophysiological mechanism.
The case of a man with a giant macular hole of the right eye is described with visual acuity, fundus photographs and spectral domain ocular coherence tomography.
A 56-year-old man with Alport syndrome and giant macular hole (2291 μm × 2265 μm) in his right eye, reducing the visual acuity to 20/200, complained of progressive visual loss in his contralateral eye. Fundus examination of the left eye revealed a circular perimacular atrophy.
Giant macular holes are one possible retinal complication of Alport syndrome. Their pathogenesis differs from idiopathic macular holes and may result from the combination of collagen type IV abnormalities in the basement membranes of both Bruch's membrane and the internal limiting membrane, along with anomalous vitreo-retinal adhesion.
Alport综合征是一种进行性遗传性肾小球肾炎,可导致肾衰竭、听力丧失和眼部病变。
报告1例Alport综合征患者发生巨大黄斑裂孔的病例,复习相关文献,并提出病理生理机制。
通过视力、眼底照片和频域光学相干断层扫描描述1例右眼患有巨大黄斑裂孔男性患者的病例。
1例56岁患有Alport综合征的男性患者,右眼有巨大黄斑裂孔(2291μm×2265μm),视力降至20/200,其对侧眼出现进行性视力丧失。左眼眼底检查发现黄斑周围呈圆形萎缩。
巨大黄斑裂孔是Alport综合征可能出现的一种视网膜并发症。其发病机制不同于特发性黄斑裂孔,可能是由于布鲁赫膜和内界膜基底膜中IV型胶原异常,以及玻璃体视网膜异常粘连共同作用的结果。