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隐性X连锁鱼鳞病与寻常型鱼鳞病临床诊断的准确性。

Accuracy of the clinical diagnosis of recessive X-linked ichthyosis vs ichthyosis vulgaris.

作者信息

Cuevas-Covarrubias S A, Kofman-Alfaro S H, Palencia A B, Díaz-Zagoya J C

机构信息

Servicio de Genética, Hospital General de México, Facultad de Medicina, UNAM, D.F., México.

出版信息

J Dermatol. 1996 Sep;23(9):594-7. doi: 10.1111/j.1346-8138.1996.tb02660.x.

DOI:10.1111/j.1346-8138.1996.tb02660.x
PMID:8916657
Abstract

The present study analyzes the accuracy of the clinical diagnosis of X-linked ichthyosis (XLI) vs ichthyosis vulgaris (IV), in a sample of Mexican patients. The study was double blind, using steroid sulfatase (STS) activity as the golden standard. Twenty male patients were included; 16 corresponded to XLI and 4 to IV. The clinical diagnosis was correct in 9 of the 16 XLI cases (56%) and in 2 of the 4 IV cases (50%). Some clinical findings in XLI, such as cryptorchidism in patients and delayed labor in their mothers, were important features for diagnosis. Statistical analysis of the results showed: among physicians (n = 2) Kappa value 0.50, specific concordance 0.40, and absolute concordance 0.75; other values were sensibility 0.56, specificity 0.50, positive predictive value 0.82, negative predictive value 0.22, accuracy 0.55, prevalence 0.80. In conclusion, the differential diagnosis of XLI and IV is very difficult, and we consider that this is not explained either by personal skills or by other conditions. It could be attributed to the similarities in skin manifestations of these two diseases. The performance of the STS assay is imperative in order to correctly diagnose the disease and offer adequate genetic counseling.

摘要

本研究分析了墨西哥患者样本中X连锁鱼鳞病(XLI)与寻常型鱼鳞病(IV)临床诊断的准确性。该研究为双盲研究,使用类固醇硫酸酯酶(STS)活性作为金标准。纳入了20名男性患者;其中16例为XLI,4例为IV。16例XLI病例中有9例(56%)临床诊断正确,4例IV病例中有2例(50%)临床诊断正确。XLI的一些临床发现,如患者隐睾症及其母亲分娩延迟,是诊断的重要特征。结果的统计分析显示:医生(n = 2)之间的Kappa值为0.50,特异性一致性为0.40,绝对一致性为0.75;其他值为敏感性0.56、特异性0.50、阳性预测值0.82、阴性预测值0.22、准确性0.55、患病率0.80。总之,XLI和IV的鉴别诊断非常困难,我们认为这既不能用个人技能也不能用其他条件来解释。这可能归因于这两种疾病皮肤表现的相似性。为了正确诊断疾病并提供充分的遗传咨询,进行STS检测是必不可少的。

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