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富克斯异色性睫状体炎的临床分析

Clinical analysis of Fuchs' heterochromic cyclitis.

作者信息

La Hey E, Baarsma G S, De Vries J, Kijlstra A

机构信息

The Netherlands Ophthalmic Research Institute, Amsterdam.

出版信息

Doc Ophthalmol. 1991;78(3-4):225-35. doi: 10.1007/BF00165685.

DOI:10.1007/BF00165685
PMID:1790745
Abstract

Fuchs' heterochromic cyclitis (FHC) is an important diagnosis to make. Not only for the patient, because incorrect diagnosis may lead to unnecessary therapy and the failure to detect secondary glaucoma, but also for the comparison of studies on the etiology of FHC, which is still unknown. No clinical criteria for establishing the diagnosis of FHC have been internationally accepted yet. By means of clinical analyses of FHC patients in different parts of the world, predominant clinical features may be distinguished and combined to form (internationally accepted) diagnostic criteria. We report a clinical analysis of 51 FHC patients in the Netherlands. Acute symptoms (severe redness, pain or photophobia) were never (100%) encountered. Characteristic keratic precipitates (88%) and/or minimal aqueous cells and flare (60%) and/or vitreous opacities (84%) were major signs, indicating a chronic inflammatory activity, in which no synechiae (100%) were present. Heterochromia (82%) was not a constant sign, but iris stromal atrophy, which causes the heterochromia, was always present (100%). Cataract was present in 82% as a result of the chronic iridocyclitis. Secondary glaucoma was present in 22%. Based on the predominant clinical findings obtained from this analysis of FHC patients, and on data in the literature, we propose clinical diagnostic criteria for FHC. Future studies, also including other uveitis groups, are necessary to confirm these diagnostic criteria.

摘要

富克斯异色性睫状体炎(FHC)是一项需要做出的重要诊断。这不仅对患者很重要,因为错误诊断可能导致不必要的治疗以及无法检测到继发性青光眼,而且对于FHC病因研究的比较也很重要,目前FHC的病因仍不清楚。国际上尚未接受用于确立FHC诊断的临床标准。通过对世界各地FHC患者的临床分析,可以区分并综合主要临床特征以形成(国际认可的)诊断标准。我们报告了对荷兰51例FHC患者的临床分析。从未出现过急性症状(严重眼红、疼痛或畏光)(100%)。特征性角膜后沉着物(88%)和/或少量房水细胞及闪光(60%)和/或玻璃体混浊(84%)是主要体征,表明存在慢性炎症活动,其中不存在虹膜粘连(100%)。异色症(82%)并非始终存在的体征,但导致异色症的虹膜基质萎缩总是存在(100%)。由于慢性虹膜睫状体炎,82%的患者存在白内障。22%的患者存在继发性青光眼。基于对FHC患者的这一分析所获得的主要临床发现以及文献中的数据,我们提出了FHC的临床诊断标准。未来还需要开展包括其他葡萄膜炎组在内的研究来证实这些诊断标准。

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[Fuchs' heterochromic cyclitis without heterochromia: a diagnostic approach].[无虹膜异色的富克斯异色性睫状体炎:一种诊断方法]
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本文引用的文献

1
Fuchs' syndrome of heterochromic cyclitis.富克斯异色性睫状体炎综合征
AMA Arch Ophthalmol. 1955 Aug;54(2):179-86. doi: 10.1001/archopht.1955.00930020181003.
2
Signs and symptoms of uveitis. I. Anterior uveitis.葡萄膜炎的体征和症状。I. 前葡萄膜炎。
Am J Ophthalmol. 1959 May;47(5 Pt 2):155-70. doi: 10.1016/s0002-9394(14)78239-x.
3
Fuchs' heterochromic cyclitis and ocular toxoplasmosis.富克斯异色性睫状体炎与眼弓形体病
Immunol Rev. 2024 Mar;322(1):113-137. doi: 10.1111/imr.13290. Epub 2023 Nov 27.
4
Comparison Between Two Types of Viral-Induced Anterior Uveitis In Vitro and In Vivo: A Stronger Response in Herpes Simplex Virus Type 1 Than in Murine Cytomegalovirus.两种病毒诱导的前葡萄膜炎的体外与体内比较:单纯疱疹病毒 1 型比鼠巨细胞病毒引起的反应更强。
Invest Ophthalmol Vis Sci. 2023 Nov 1;64(14):20. doi: 10.1167/iovs.64.14.20.
5
Overview and update on cytomegalovirus-associated anterior uveitis and glaucoma.巨细胞病毒相关性前葡萄膜炎和青光眼的概述及最新进展。
Front Public Health. 2023 Mar 1;11:1117412. doi: 10.3389/fpubh.2023.1117412. eCollection 2023.
6
Factors associated with low prevalence of Fuchs' uveitis syndrome in Japan.日本富克斯葡萄膜炎综合征低患病率相关因素。
Front Med (Lausanne). 2022 Sep 30;9:999804. doi: 10.3389/fmed.2022.999804. eCollection 2022.
7
Detection of Fuchs' Uveitis Syndrome From Slit-Lamp Images Using Deep Convolutional Neural Networks in a Chinese Population.在中国人群中使用深度卷积神经网络从裂隙灯图像检测Fuchs葡萄膜炎综合征
Front Cell Dev Biol. 2021 Jun 18;9:684522. doi: 10.3389/fcell.2021.684522. eCollection 2021.
8
Development of revised diagnostic criteria for Fuchs' uveitis syndrome in a Chinese population.修订的中国人 Fuchs 葡萄膜炎综合征诊断标准的制定。
Br J Ophthalmol. 2022 Dec;106(12):1678-1683. doi: 10.1136/bjophthalmol-2021-319343. Epub 2021 Jun 9.
9
Incidence and changing patterns of uveitis in Central Tokyo.东京都中心葡萄膜炎的发病情况及变化模式。
Int Ophthalmol. 2021 Jul;41(7):2377-2388. doi: 10.1007/s10792-021-01791-4. Epub 2021 May 28.
10
Evaluation of radial peripapillary capillary density in patients with Fuchs uveitis syndrome.评价 Fuchs 葡萄膜炎综合征患者的视盘旁放射状毛细血管密度。
Graefes Arch Clin Exp Ophthalmol. 2019 Dec;257(12):2735-2742. doi: 10.1007/s00417-019-04491-z. Epub 2019 Oct 22.
Am J Ophthalmol. 1982 Jun;93(6):739-44. doi: 10.1016/0002-9394(82)90470-6.
4
Clinical features and prognosis in Fuchs' uveitis syndrome.富克斯葡萄膜炎综合征的临床特征与预后
Arch Ophthalmol. 1982 Oct;100(10):1622-6. doi: 10.1001/archopht.1982.01030040600009.
5
Chorioretinal scars in Fuchs' heterochromic iridocyclitis.富克斯异色性虹膜睫状体炎中的脉络膜视网膜瘢痕
Arch Ophthalmol. 1984 Aug;102(8):1153-5. doi: 10.1001/archopht.1984.01040030931016.
6
Fuchs's heterochromic cyclitis: A critical review of the literature. I. Clinical characteristics of the syndrome.富克斯异色性睫状体炎:文献综述。I. 该综合征的临床特征
Surv Ophthalmol. 1973 May-Jun;17(6):394-457.
7
Doyne lecture. Heterochromic iridocyclitis.多伊内讲座。异色性虹膜睫状体炎。
Trans Ophthalmol Soc U K (1962). 1985;104 ( Pt 3):219-31.
8
Lens Opacities Classification System.晶状体混浊分类系统
Arch Ophthalmol. 1988 Mar;106(3):330-4. doi: 10.1001/archopht.1988.01060130356020.
9
Fuchs' heterochromic iridocyclitis in blacks.黑人中的富克斯异色性虹膜睫状体炎
Arch Ophthalmol. 1988 Dec;106(12):1688-90. doi: 10.1001/archopht.1988.01060140860027.
10
Glaucoma in patients with uveitis.葡萄膜炎患者的青光眼
Br J Ophthalmol. 1990 Apr;74(4):223-7. doi: 10.1136/bjo.74.4.223.