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Fuchs虹膜异色性睫状体炎不是很少见的疾病。发生漏诊的原因可能是虹膜异色不明显,尤其在棕色虹膜的人。因此,Franceschetti(1955)建议使用Fuchs综合征的名称,其诊断依据系虹膜萎缩性改变。角膜后沉着物、前房内有极少量细胞和闪光、玻璃体内有细胞、无虹膜后粘连,以及常合并有白内障和青光眼。对此种病人视力的最终预后是有争论的。本文对诊断为Fuchs综合征的54例病人的临床特征和病程作一摘要报告。一、材料和方法:把Mayo门诊部1950至1980年间诊断为Fuchs虹膜异色性睫状体炎的全部病人均复习了病史资料,并发出了随访信,
Fuchs iris Xenochromatitis is not a rare disease. The cause of missed diagnosis may be inconspicuous iris color, especially in people with brown iris. Therefore, Franceschetti (1955) recommended the use of Fuchs syndrome name, the diagnosis based on iris atrophy changes. Posterior corneal deposition, a very small amount of cells in the anterior chamber and flash, cells in the vitreous, no post-iris adhesions, and often associated with cataracts and glaucoma. The final prognosis of this patient’s vision is controversial. In this paper, 54 patients diagnosed as Fuchs syndrome clinical features and duration of a summary report. MATERIALS AND METHODS: All patients diagnosed with Fuchs iris Xenoochromatosis from 1950 to 1980 in Mayo Clinic reviewed their medical history and sent out follow-up letters,