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系统性红斑狼疮中具有临床意义的心脏瓣膜病。

Clinically significant valvular heart disease in systemic lupus erythematosus.

作者信息

Straaton K V, Chatham W W, Reveille J D, Koopman W J, Smith S H

机构信息

Department of Medicine, University of Alabama, Birmingham 35294.

出版信息

Am J Med. 1988 Nov;85(5):645-50. doi: 10.1016/s0002-9343(88)80236-5.

Abstract

PURPOSE

Clinically significant valvular heart disease due to systemic lupus erythematosus (SLE) has generally been considered rare, and Libman-Sacks endocarditis has been thought to be predominantly an autopsy finding. With the declining prevalence of rheumatic heart disease, however, the spectrum of valvular heart disease is changing. We retrospectively analyzed our experience with SLE between 1975 and 1987 for the presence of hemodynamically significant valvular heart disease.

PATIENTS AND METHODS

An existing data base of 421 patients with SLE was selected for review. Patients were selected for inclusion in the study if they met four or more of the criteria of the American Rheumatism Association for SLE, they had clinically significant valvular heart disease, and tissue from the involved valve was available for review. The etiology of the valve lesion was determined by assessment of the clinical history, chart review, gross morphology, and valve histology.

RESULTS

Of 14 cases with pathologic material available for review, six had anatomic features of SLE valvular heart disease such as verrucous vegetations or valvulitis with necrosis and vasculitis. Two of these patients underwent successful valve replacements and four died from complications of their valve disease.

CONCLUSION

We suggest that significant morbidity and mortality may result from SLE valvular heart disease in about 1 to 2 percent of SLE patients and that the pathogenetic mechanisms underlying valve dysfunction in SLE patients are multifactorial.

摘要

目的

系统性红斑狼疮(SLE)所致具有临床意义的瓣膜性心脏病通常被认为较为罕见,而Libman-Sacks心内膜炎一直被认为主要是尸检时的发现。然而,随着风湿性心脏病患病率的下降,瓣膜性心脏病的范围正在发生变化。我们回顾性分析了1975年至1987年间我们诊治SLE患者时存在血流动力学显著改变的瓣膜性心脏病的经验。

患者与方法

选取一个包含421例SLE患者的现有数据库进行回顾。如果患者符合美国风湿病协会SLE标准中的四项或更多项、患有具有临床意义的瓣膜性心脏病且受累瓣膜的组织可供检查,则将其纳入本研究。通过评估临床病史、病历审查、大体形态和瓣膜组织学来确定瓣膜病变的病因。

结果

在14例有病理材料可供检查的病例中,6例具有SLE瓣膜性心脏病的解剖学特征,如疣状赘生物或伴有坏死和血管炎的瓣膜炎症。其中2例患者成功进行了瓣膜置换,4例死于瓣膜疾病的并发症。

结论

我们认为,约1%至2%的SLE患者可能因SLE瓣膜性心脏病导致严重的发病率和死亡率,且SLE患者瓣膜功能障碍的发病机制是多因素的。

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