Babalola O E, Murdoch I E
Rachel Eye Center, Abuja, Nigeria.
Cornea. 2001 Mar;20(2):183-6. doi: 10.1097/00003226-200103000-00015.
We report an unusual type of corneal change in some communities mesoendemic for onchocerciasis in Kaduna State of Northern Nigeria.
Thirty-four villages with an overall average microfilarial skin snip positivity rate of 71% and a total population of about 10,000 were included in a controlled trial of ivermectin for onchocerciasis. Detailed slit lamp examination of 806 persons within this population revealed at least 27 individuals with these lesions. There were 11 women and 16 men, aged between 5 and 70 years with a mean age of 45 years and a SD of 15 years. Drawings and photographs of 22 of these individuals were available for assessment.
The lesions were peripheral, silvery white, and of two main types: the first group's lesions were flaky, refractile, and crystalline in appearance; the second group's lesions were more cylindrical in outline and were crisscrossed, giving a lattice-like pattern. There were indeterminate forms in between these polar topographies. Of the 25 subjects who had skin snips performed, 23 were microfilaria-positive. There was no accompanying inflammation and the posterior segments showed no evidence of crystalline deposits or retinitis pigmentosa, as is found in Bietti's dystrophy. The lesions coexisted with typical sclerosing keratitis in six individuals, and changes noted in the posterior pole of ten individuals were typical of onchocercal chorioretinitis. The evidence for consanguinity was not compelling. Differences between and similarities to Bietti's and Schnyder's crystalline corneal dystrophy, which are known to be composed of cholesterol crystals, are discussed. The lesions are also compared with lattice dystrophy known to be composed of amyloid. These lesions may be related to onchocercal infection.
We describe some unusual peripheral corneal changes in individuals living within areas of Northern Nigeria mesoendemic for onchocerciasis. These changes take the form of flaky crystals or lattice within the anterior stroma and are common in middle-aged individuals. This may be related to onchocercal infection.
我们报告了在尼日利亚北部卡杜纳州盘尾丝虫病中度流行的一些社区中出现的一种不寻常的角膜变化类型。
34个村庄纳入了伊维菌素治疗盘尾丝虫病的对照试验,这些村庄的微丝蚴皮肤切片总体平均阳性率为71%,总人口约10,000人。对该人群中的806人进行了详细的裂隙灯检查,发现至少27人有这些病变。其中有11名女性和16名男性,年龄在5至70岁之间,平均年龄45岁,标准差15岁。有22人的绘图和照片可供评估。
病变位于周边,呈银白色,主要有两种类型:第一组病变外观呈片状、有折光性且似晶体;第二组病变轮廓更呈圆柱形,相互交错,形成格子状图案。在这些极端形态之间存在不确定形式。在进行皮肤切片检查的25名受试者中,23人微丝蚴呈阳性。没有伴随炎症,且后节未显示出比埃蒂营养不良中所见的晶体沉积或色素性视网膜炎的证据。这些病变在6名个体中与典型的硬化性角膜炎共存,在10名个体后极观察到的变化是盘尾丝虫性脉络膜视网膜炎的典型表现。近亲结婚的证据并不确凿。讨论了与已知由胆固醇晶体组成的比埃蒂和施奈德结晶性角膜营养不良的异同。还将这些病变与已知由淀粉样蛋白组成的格子状营养不良进行了比较。这些病变可能与盘尾丝虫感染有关。
我们描述了尼日利亚北部盘尾丝虫病中度流行地区居民中一些不寻常的周边角膜变化。这些变化表现为前基质内的片状晶体或格子状,在中年个体中很常见。这可能与盘尾丝虫感染有关。