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抗磷脂综合征的皮肤表现:200例连续病例

Dermatologic manifestations of the antiphospholipid syndrome: two hundred consecutive cases.

作者信息

Francès Camille, Niang Suzanne, Laffitte Emmanuel, Pelletier Francois le, Costedoat Nathalie, Piette Jean Charles

机构信息

Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

出版信息

Arthritis Rheum. 2005 Jun;52(6):1785-93. doi: 10.1002/art.21041.

Abstract

OBJECTIVE

To describe dermatologic manifestations of the antiphospholipid syndrome (APS) and to investigate possible correlations between livedo reticularis and other APS manifestations.

METHODS

We conducted a single-center study of 200 consecutive patients with primary or systemic lupus erythematosus-related APS. To qualify for the study, patients had to fulfill clinical and laboratory criteria from the most recent international consensus statement on classification of definite APS. Dermatologic manifestations were systematically evaluated by a dermatologist. Only dermatologic lesions that may be related to APS were included in the analyses. Correlations between livedo reticularis and other APS manifestations were determined using Fisher's 2-tailed, chi-square, and nonparametric Mann-Whitney tests.

RESULTS

Dermatologic manifestations were noted in 49% of the patients and were the presenting manifestations in 30.5%. Livedo reticularis was the most frequent manifestation, observed in 25.5% of the patients. Livedo reticularis was shown to be significantly associated with cerebral or ocular ischemic arterial events (odds ratio [OR] 10.8, 95% confidence interval [95% CI] 5.2-22.5), seizures (OR 6.5, 95% CI 2.6-16), all arterial events (OR 6, 95% CI 2.9-12.6), heart valve abnormalities detected on echocardiography (OR 7.3, 95% CI 3.6-14.7), and arterial systemic hypertension (>/=160/90 mm Hg) (OR 2.9, 95% CI 1.5-5.7). Conversely, it was observed with decreased frequency in patients with only venous thrombosis (OR 0.2, 95% CI 0.1-0.5).

CONCLUSION

The dermatologic manifestations of APS are frequently the presenting feature of the syndrome, and livedo reticularis is significantly associated with the arterial subset of APS.

摘要

目的

描述抗磷脂综合征(APS)的皮肤表现,并研究网状青斑与其他APS表现之间可能存在的相关性。

方法

我们对200例连续的原发性或与系统性红斑狼疮相关的APS患者进行了单中心研究。为符合研究条件,患者必须满足最新的关于明确APS分类的国际共识声明中的临床和实验室标准。由皮肤科医生对皮肤表现进行系统评估。分析中仅纳入可能与APS相关的皮肤病变。使用Fisher双侧检验、卡方检验和非参数Mann-Whitney检验确定网状青斑与其他APS表现之间的相关性。

结果

49%的患者出现皮肤表现,其中30.5%为首发表现。网状青斑是最常见的表现,见于25.5%的患者。网状青斑与脑或眼部缺血性动脉事件(比值比[OR] 10.8,95%置信区间[95%CI] 5.2 - 22.5)、癫痫发作(OR 6.5,95%CI 2.6 - 16)、所有动脉事件(OR 6,95%CI 2.9 - 12.6)、超声心动图检测到的心脏瓣膜异常(OR 7.3,95%CI 3.6 - 14.7)以及动脉性系统性高血压(≥160/90 mmHg)(OR 2.9,95%CI 1.5 - 5.7)显著相关。相反,仅患有静脉血栓形成的患者中其出现频率降低(OR 0.2,95%CI 0.1 - 0.5)。

结论

APS的皮肤表现常常是该综合征的首发特征,且网状青斑与APS的动脉型显著相关。

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