首页> 美国卫生研究院文献>Clinical and Developmental Immunology >Uniphasic Blanching of the Fingers Abnormal Capillaroscopy in Nonsymptomatic Digits and Autoantibodies: Expanding Options to Increase the Level of Suspicion of Connective Tissue Diseases beyond the Classification of Raynauds Phenomenon
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Uniphasic Blanching of the Fingers Abnormal Capillaroscopy in Nonsymptomatic Digits and Autoantibodies: Expanding Options to Increase the Level of Suspicion of Connective Tissue Diseases beyond the Classification of Raynauds Phenomenon

机译:手指单相变白无症状数字的异常毛细血管镜检查和自身抗体:扩大选择范围以增加对结缔组织疾病的怀疑程度超越雷诺现象的分类

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摘要

In patients with Raynaud's phenomenon (RP), the role of medical history, capillaroscopy, and autoantibodies in order to provide an early diagnosis of connective tissue disease (CTD) were examined. 115 consecutive adults with uni-, bi-, or triphasic colour changes of the fingers were studied. RP was bilateral in 92.7% of patients. The middle finger was significantly more affected. A lack of association between fingers affected by RP and fingers with capillary abnormalities was observed OR = 0.75 (0.34–1.66). RP with the cyanotic phase had a higher risk at capillaroscopy to have hemorrhages OR = 4.46 (1.50–13.30) and giant capillaries OR = 24.85 (1.48–417.44). The thumb and triphasic involvement have an OR of 1.477 and 1.845, respectively. RP secondary to systemic sclerosis (SSc) had greater value of VAS pain (p = 0.011). The presence of anti-centromere antibodies was significantly associated with a higher risk of SSc (p < 0.001). 44.3% of subjects had uniphasic blanching of the fingers, and among these, 27% was diagnosed as having an overt or suspected CTD. Markers of a potential development of CTDs include severe RP symptoms, positive autoantibodies, and capillary abnormalities. These data support the proposal to not discharge patients with uniphasic blanching of the fingers to avoid missing the opportunity of an early diagnosis.
机译:在患有雷诺现象(RP)的患者中,检查了病史,毛细血管镜检查和自身抗体的作用,以便对结缔组织病(CTD)进行早期诊断。研究了115位连续的手指单,双或三色颜色变化的成年人。 RP在92.7%的患者中为双侧。中指的受影响明显更大。观察到受RP影响的手指与毛细血管异常的手指之间缺乏关联,或OR = 0.75(0.34–1.66)。紫otic期的RP在毛细血管镜检查中具有较高的风险,即出血或= 4.46(1.50–13.30)和巨毛细管或= 24.85(1.48–417.44)。拇指和三角肌的OR分别为1.477和1.845。继发于系统性硬化症(SSc)的RP具有更大的VAS疼痛值(p = 0.011)。抗着丝粒抗体的存在与SSc的较高风险显着相关(p <0.001)。 44.3%的受试者手指单相变白,其中27%被诊断为明显的CTD或疑似CTD。 CTD潜在发展的标志包括严重的RP症状,阳性自身抗体和毛细血管异常。这些数据支持不让手指单相变白的患者出院以避免丢失早期诊断机会的建议。

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