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成人斯蒂尔病并发肺动脉高压。

Pulmonary arterial hypertension complicating adult-onset Still's disease.

机构信息

Department of Rheumatology, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, India.

出版信息

Clin Rheumatol. 2013 Mar;32 Suppl 1:S1-2. doi: 10.1007/s10067-009-1230-z. Epub 2009 Aug 11.

Abstract

Adult-onset Still's disease (AOSD) is a rare condition diagnosed by a combination of clinical and laboratory features and after ruling out other conditions. Pulmonary manifestations, apart from pleuritis, are uncommon and pulmonary arterial hypertension (PAH) in extremely uncommon. We have described a case of AOSD with severe PAH. There have been rare reports of PAH occurring in AOSD in the literature. Probably, this manifestation may have been understudied, being confined to cases which are symptomatic. A larger study to look at the asymptomatic occurrences of PAH in AOSD may help in unraveling the mystery of this disease.

摘要

成人Still 病(AOSD)是一种罕见的疾病,通过临床和实验室特征的综合诊断,并排除其他疾病后得出诊断。除胸膜炎外,肺部表现并不常见,肺动脉高压(PAH)极为罕见。我们描述了一例伴有严重 PAH 的 AOSD 病例。文献中罕见有 AOSD 合并 PAH 的报道。可能这种表现可能研究不足,仅限于有症状的病例。更大规模的研究观察 AOSD 中无症状 PAH 的发生情况,可能有助于揭示这种疾病的奥秘。

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