Lubiński Wojciech, Gosławski Wojciech, Penkala Krzysztof, Drobek-Słowik Monika, Karczewicz Danuta
Department of Ophthalmology, Pomeranian Medical University, Powstańców Wlkp. 72 str., 70-111 Szczecin, Poland.
Doc Ophthalmol. 2008 Mar;116(2):111-8. doi: 10.1007/s10633-007-9086-5. Epub 2007 Oct 23.
Occult macular dystrophy (OMD) is an unusual, inherited macular dystrophy characterized by a slowly progressive decline of visual acuity with normal fundus and fluorescein angiography (FA). The authors present a 43-year-old man who was diagnosed as having OMD because of the results of electrophysiological, psychophysical, optical coherence tomography (OCT) tests.
Routine ophthalmological evaluation, FA, visual field tests, electroretinographic examinations (EOG, ERG, PERG and mfERG recordings according to ISCEV standards) and foveal thickness measurements (OCT) were performed.
Funduscopic examinations, FA, full field ERG as well as PERG results were all normal. In both eyes, the abnormalities were observed in static perimetry (relative central scotomas), mfERG (significant reduction of P1 amplitude in the central retinas) and OCT (significantly thinner foveal thickness).
A new case with OMD is added to preceding reports. The mfERG and OCT tests are important in detection of OMD patients. It can help in differential diagnosis of amblyopia, optic nerve diseases and non-organic visual disorders.
隐匿性黄斑营养不良(OMD)是一种罕见的遗传性黄斑营养不良,其特征是视力缓慢进行性下降,眼底和荧光素血管造影(FA)正常。作者报告了一名43岁男性,因其电生理、心理物理学、光学相干断层扫描(OCT)检查结果而被诊断为OMD。
进行了常规眼科评估、FA、视野检查、视网膜电图检查(根据国际临床视觉电生理学会标准进行EOG、ERG、PERG和mfERG记录)以及黄斑中心凹厚度测量(OCT)。
眼底检查、FA、全视野ERG以及PERG结果均正常。双眼在静态视野检查(相对中心暗点)、mfERG(中心视网膜P1波幅显著降低)和OCT(黄斑中心凹厚度显著变薄)中观察到异常。
在之前的报告基础上增加了一例OMD新病例。mfERG和OCT检查对OMD患者的检测很重要。它有助于弱视、视神经疾病和非器质性视觉障碍的鉴别诊断。