重度虹膜角膜角色素沉着和青光眼与氟中毒有关

E. Aytuluner, E. Mensiz
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引用次数: 2

摘要

地方性氟中毒是一种慢性致残骨骼和牙齿疾病,由摄入或吸入大量氟化物引起。虽然这种疾病的流行率已大大下降,但在世界某些地区仍时有发生。我省伊斯帕塔省是一个自然发生的地方性氟中毒地区。本研究的目的是探讨一组氟中毒患者的眼部表现。研究对象为50例(32例F, 18例M),年龄29 ~ 74岁(54.44±12.28),均为地方性氟中毒患者。选择年龄和性别匹配的连续50例无氟中毒临床表现的患者作为对照。氟中毒患者和不氟中毒患者均行常规眼科检查。为了评估前房角色素沉着的程度,我们根据Pantone®颜色配方指南中选择的棕色组成了一个评分系统(从1到4)。两组在血清、尿液和水中氟化物水平方面的差异具有统计学意义(均p0.05)。我们认为重度小梁色素沉着可能是地方性氟中毒的一个特征。在没有虹膜色素分散的病因和症状的氟中毒患者的病理性小梁色素沉着的鉴别诊断中,应牢记这种疾病。我们还提出地方性氟中毒可能导致或加重青光眼的严重程度。为了了解地方性氟中毒患者小梁改变的确切机制,需要进一步的研究。
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HEAVY IRIDOCORNEAL ANGLE HYPERPIGMENTATION AND GLAUCOMA ASSOCIATED WITH FLUOROSIS
Endemic fluorosis is a chronic crippling skeletal and dental disease caused by ingestion or inhalation of large amounts of fluoride. Although the prevalence of this disease has decreased considerably, it still occurs in some parts of the world. Our province Isparta is a naturally occurring endemic fluorosis area. The aim of this study is to investigate the ocular manifestations of the disorder in a group of patients with fluorosis. Fifty (32 F, 18 M) consecutive patients, ages ranging between 29 and 74 years (54.44±12.28), with endemic fluorosis constituted the study group. Age and sex matched fifty consecutive patients without clinical findings of fluorosis were selected as controls. Patients with and without fluorosis underwent a routine ophthalmologic examination. To assess the levels of hyperpigmentation in anterior chamber angle, we constituted a grading system (from 1 to 4) based on selected brownish colors from Pantone® Color Formula Guide. The differences between two groups with respect to serum, urine, and water fluoride levels are statistically significant (for all p<0.001). With respect to iridocorneal angle hyperpigmentation (ICA HP) grades, the difference between fluorosis and control group was statistically significant (p<0.001). In the fluorosis group, we observed eight cases (16%) of open angle glaucoma (OAG). Remarkably, ICA HP grade was 4+ in six out of eight cases; this finding was statistically significant (p<0.001). The remaining two showed grade 1+ ICA HP. Difference between number of cataracts or previous cataract operations of the two groups [fluorosis group: 15 cases (30%), controls: 12 cases (24%)] was not statistically significant (p>0.05). We suggest that heavy trabecular hyperpigmentation appearance may be a feature of endemic fluorosis. This disorder should be kept in mind in differential diagnosis of pathologic trabecular hyperpigmentation in patients with fluorosis and without the causes and symptoms of iris pigment dispersion. We also propose that endemic fluorosis may lead or augment the severity of glaucoma. Further studies are warranted in order to comprehend the exact mechanism of trabecular changes in patients with endemic fluorosis.
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