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Pulmonary hypertension in MCTD: report of two cases with anticardiolipin antibody.

作者信息

Miyata M, Kida S, Kanno T, Suzuki K, Watanabe H, Kaise S, Nishimaki T, Hosoda Y, Kasukawa R

机构信息

Second Department of Internal Medicine, Fukushima Medical College, Japan.

出版信息

Clin Rheumatol. 1992 Jun;11(2):195-201. doi: 10.1007/BF02207956.

Abstract

We report on 2 patients with well-documented mixed connective tissue disease (MCTD) accompanied by severe pulmonary hypertension (PH) due to thrombosis or thromboembolism. In a previous report we indicated (1) that patients with MCTD complicated by PH have a significantly worse prognosis than patients with other connective tissue disease (CTD) complicated by PH. Both our patients had anticardiolipin antibody (a-CL) in the initial stages of the disease. We also studied the relationship of a-CL to PH in patients with other CTD. Patients of either MCTD or SLE with high levels of a-CL had significantly higher values of mean pulmonary arterial pressure than patients without a-CL. Several factors were suggested for the pathogenesis of PH such as vasospasm, arteritis, platelet dysfunction, and thrombosis or thromboembolism. The presence of a-CL may be one of important factors in development of PH among patients with MCTD with recurrent pulmonary thrombosis or thromboembolism.

摘要

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