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[疱疹性葡萄膜炎和角膜葡萄膜炎的诊断]

[Diagnosis of herpetic uveitis and keratouveitis].

作者信息

Schacher S, Garweg J G, Russ C, Böhnke M

机构信息

Universitäts-Augenklinik, Inselspital, Bern.

出版信息

Klin Monbl Augenheilkd. 1998 May;212(5):359-62. doi: 10.1055/s-2008-1034906.

Abstract

BACKGROUND

In epithelial viral keratitis as in viral retinitis, the diagnosis is made on the basis of typical clinical findings. A laboratory confirmation is achieved in over 80% using routine laboratory methods. In contrast, it is almost impossible to confirm the diagnosis of stromal herpetic keratitis in vivo using the currently available laboratory methods. Nothing is known about the situation in cases of viral anterior uveitis.

METHODS

Of 52 patients with granulomatous anterior uveitis, 31 were diagnosed on the basis of clinical findings as active herpetic uveitis (group 1), 14 as active granulomatous uveitis of unknown origin (group 2), and 7 had inactive disease after quietening down of herpetic uveitis (group 3). From all patients, aqueous humor was collected at the time of diagnosis and processed for viral culture, Herpes antigen ELISA, and amplification of viral DNA of HSV-1 and VZV.

RESULTS

Viral growth in culture was found in only one case in group 3. In this group, viral antigen or viral DNA were detected in no case. Herpes antigen was found in 5/31 cases (16%) in group 1 and in 1/11 cases (9%) in group 2, and viral DNA was found in 8/31 cases from group 1 (5x HSV-1 and 3x VZV) and in 5/14 cases (31%) from group 2. After combination of antigen detection and DNA amplification, the presence of virus was confirmed in 14/45 cases (29%).

CONCLUSION

Virus culture has not proven useful in the diagnosis of viral anterior segment disease. Despite their high overall sensitivity, neither antigen ELISA nor the amplification of viral DNA proved sensitive enough to establish a viral etiology. Nevertheless, a laboratory confirmation should be attempted in granulomatous uveitis of unknown origin after preclusion of an underlying systemic disease because of the consequences of a diagnosis of viral anterior segment disease for treatment and prognosis.

摘要

背景

在上皮性病毒性角膜炎和病毒性视网膜炎中,诊断基于典型的临床发现。使用常规实验室方法,超过80%的病例可获得实验室确诊。相比之下,使用目前可用的实验室方法在体内确诊基质性疱疹性角膜炎几乎是不可能的。对于病毒性前葡萄膜炎病例的情况则一无所知。

方法

在52例肉芽肿性前葡萄膜炎患者中,31例根据临床发现被诊断为活动性疱疹性葡萄膜炎(第1组),14例为病因不明的活动性肉芽肿性葡萄膜炎(第2组),7例在疱疹性葡萄膜炎病情缓解后处于非活动性疾病状态(第3组)。在诊断时从所有患者收集房水,并进行病毒培养、疱疹抗原酶联免疫吸附测定(ELISA)以及单纯疱疹病毒1型(HSV-1)和水痘-带状疱疹病毒(VZV)病毒DNA的扩增。

结果

仅在第3组的1例病例中发现病毒在培养中生长。在该组中,未检测到病毒抗原或病毒DNA。在第1组的5/31例(16%)病例和第2组的1/11例(9%)病例中发现疱疹抗原,在第1组的8/31例(5例HSV-1和3例VZV)病例和第2组的5/14例(31%)病例中发现病毒DNA。在抗原检测和DNA扩增相结合后,45例中的14例(29%)确诊有病毒存在。

结论

病毒培养在病毒性眼前节疾病的诊断中未被证明有用。尽管抗原ELISA和病毒DNA扩增总体敏感性较高,但两者都不足以敏感地确定病毒病因。然而,由于病毒性眼前节疾病的诊断对治疗和预后的影响,在排除潜在的全身性疾病后,对于病因不明的肉芽肿性葡萄膜炎应尝试进行实验室确诊。

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