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结节型角膜营养不良,属较少见的遗传性角膜病,国内仅有零星病理资料报道,我室曾先后遇到10例,现将其临床病理资料扼要分析如下: 临床资料10例中男性8例,女性仅2例。年令从22～64岁(平均30.8岁)病程为8～30年不等(平均17.5年)。眼科所见:为重症病例,侵犯双眼,伴有严重视力障碍(最好的一例视力仅有0.08)。角膜呈灰白色点状、环状和结节状不透明混浊区,甚至呈片状混浊,以角膜中央病灶最明显。在周边部仍或多或少留有透明区。
Nodular corneal dystrophy, is a rare hereditary keratopathy, domestic only sporadic pathological data reported, I have met in our room 10 cases, now its clinical and pathological data brief analysis is as follows: 10 cases of clinical data of men 8 cases, only 2 cases of women. Years from 22 to 64 years (mean 30.8 years) duration of 8 to 30 years (average 17.5 years). Ophthalmology seen: Severe cases of infringement of both eyes, accompanied by serious vision disorders (the best case of vision was only 0.08). Corneal gray spots, ring and nodular opaque opacity, and even flake opacity, the most obvious central corneal lesions. In the peripheral part is still more or less transparent area.