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在以肺部为主的结缔组织病中,非特异性间质性肺炎与机化性肺炎重叠。

Nonspecific interstitial pneumonia overlaps organizing pneumonia in lung-dominant connective tissue disease.

作者信息

Li Xue-Ren, Peng Shou-Chun, Wei Lu-Qing

机构信息

Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Logistics University of Chinese People's Armed Police Force P. R. China.

出版信息

Int J Clin Exp Pathol. 2015 Sep 1;8(9):11230-5. eCollection 2015.

Abstract

Here, we reported two cases of nonspecific interstitial pneumonia overlap organizing pneumonia (NSIP/OP) with lung-dominant connective tissue disease (LD-ILD). The first case is a patient with hands of chapped skin, right-sided pleuritic chest discomfort, weakness, positive ANA and antibodies to Ro/SS-A (+++) and Ro-52 (++). In the second case, there were Reynaud's disease, and nucleolus-ANA increased (1:800). Chest high resolution CT scan in both cases showed ground-glass opacifications, predominantly in basal and subpleural region and the pathologic manifestation were correlated with NSIP/OP, which were previously discovered in Sjogren syndrome, PM/DM and other rheumatic diseases. The two cases of NSIP/OP with LD-CTD we reported expand disease spectrum of NSIP/OP pathological types in ILD. However, it is necessary to process large-scale studies.

摘要

在此,我们报告了两例非特异性间质性肺炎重叠机化性肺炎(NSIP/OP)合并以肺部为主的结缔组织病(LD-ILD)的病例。第一例患者双手皮肤皲裂、右侧胸膜炎性胸痛、乏力,抗核抗体(ANA)及抗Ro/SS-A抗体(+++)和Ro-52抗体(++)阳性。第二例患者有雷诺病,核仁型ANA升高(1:800)。两例患者的胸部高分辨率CT扫描均显示磨玻璃影,主要位于基底段和胸膜下区域,病理表现与NSIP/OP相关,此前在干燥综合征、皮肌炎/多肌炎及其他风湿性疾病中也曾发现。我们报告的这两例合并LD-CTD的NSIP/OP病例扩展了ILD中NSIP/OP病理类型的疾病谱。然而,有必要进行大规模研究。

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