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[弥漫性硬皮病和CREST综合征中的肺动脉高压]

[Pulmonary hypertension in diffuse scleroderma and the CREST syndrome].

作者信息

Presetnik M, Music E, Kolsek B, Rozman B

出版信息

Plucne Bolesti. 1989 Jan-Jun;41(1-2):5-7.

PMID:2798573
Abstract

In 22 patients with systemic sclerosis (SS) i.e. 16 patients with diffuse scleroderma and 6 patients with CREST syndrome the presence of pulmonary hypertension (PH) was investigated by microcatheter. Manifest PH was found in 3 patients with diffuse scleroderma (19%) and in 3 patients with CREST syndrome (50%). Latent PH was found in 8 patients with diffuse scleroderma (50%) and in 2 patients with CREST syndrome (33%). In our patients the occurrence of PH in CREST syndrome was more frequent than in diffuse scleroderma which is in accordance with the data from the literature. Isolated PH (without simultaneous involvement of pulmonary interstitium) was found in most patients with CREST syndrome (but in 1 case) and in 3 out of 11 patients with diffuse scleroderma.

摘要

在22例系统性硬化症(SS)患者中,即16例弥漫性硬皮病患者和6例CREST综合征患者,通过微导管研究了肺动脉高压(PH)的存在情况。在3例弥漫性硬皮病患者(19%)和3例CREST综合征患者(50%)中发现了明显的PH。在8例弥漫性硬皮病患者(50%)和2例CREST综合征患者(33%)中发现了潜在的PH。在我们的患者中,CREST综合征中PH的发生率比弥漫性硬皮病更频繁,这与文献数据一致。在大多数CREST综合征患者(但有1例除外)和11例弥漫性硬皮病患者中的3例中发现了孤立性PH(不同时累及肺间质)。

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