Naumann G O, Lerche W, Schroeder W
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1976 Jul 26;200(1):39-50. doi: 10.1007/BF00411431.
The eye of a 47 year old man with tyrosinase-positive oculocutaneous albinism, photophobia, nystagmus and visual acuity 0, 4-0, 5 was histologically examined after orbital exenteration for neoplasia. Histologic serial sections of the centre of the retina showed a continuous 6-8 cell-layer of ganglion cells, without any suggestion of a foveolar pit. The outer layers of the macular retina were altered secondarily by tumor-impression-folds; they were unremarkable at the periphery as were the acid mucopolysaccharides in the receptor region. Electron microscopy of the uvea and the retinal pigment epithelium showed a normal number of pigment granules but a deficiency of melanin, as well as structural anomalies. The absence of the foveolar pit and the decrease of visual acuity in tyrosinase-positive albinism is caused by definite morphologic alteration in the arrangement of ganglion cells in the macular region in the sense of a foveolar aplasia. The etiology is discussed. An identic anomaly has been described in aniridia, similar ones in other congenital ocular diseases.
一名47岁患有酪氨酸酶阳性眼皮肤白化病、畏光、眼球震颤且视力为0.4 - 0.5的男性患者,因肿瘤行眼眶内容剜除术后,对其眼球进行了组织学检查。视网膜中央的组织学连续切片显示有一层由6 - 8个细胞层组成的连续神经节细胞层,未发现任何中央凹坑的迹象。黄斑视网膜外层因肿瘤压迫形成褶皱而继发改变;周边区域无明显异常,感受器区域的酸性粘多糖也无异常。葡萄膜和视网膜色素上皮的电子显微镜检查显示色素颗粒数量正常,但黑色素缺乏以及存在结构异常。酪氨酸酶阳性白化病中中央凹坑的缺失和视力下降是由于黄斑区神经节细胞排列出现明确的形态学改变,即中央凹发育不全。文中讨论了其病因。在无虹膜症中曾描述过相同的异常情况,在其他先天性眼病中也有类似情况。