Rapidly progressive interstitial lung disease with an organising pneumonia-dominant high-resolution computed tomography pattern in systemic lupus erythematosus: a case report and literature review.

IF 0.9 Q4 RHEUMATOLOGY
Kentaro Kuzuya, Yoshinobu Matsuura, Akito Morimoto, Norihiko Yamaguchi, Hiroyuki Yamane
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Abstract

Among pulmonary involvements of systemic lupus erythematosus (SLE), interstitial lung disease (ILD) is an infrequent but clinically significant complication, with fatal cases reported as 'acute lupus pneumonitis' and associated with increased mortality. However, SLE-ILD remains insufficiently stratified according to clinical course, and no predictive factor for rapidly progressive ILD (RP-ILD), including high-resolution computed tomography (HRCT) pattern, has yet been established. Here we report a 71-year-old man who presented with dyspnea, fever, pancytopenia, anti-double-stranded DNA antibody positivity, hypocomplementemia, proteinuria, and neuropsychiatric symptoms. HRCT initially showed bilateral consolidation predominantly in the peripheral lower lung zones, consistent with organising pneumonia (OP), followed by rapid extension with ground-glass opacities. He was diagnosed with rapidly progressive systemic lupus erythematosus-associated interstitial lung disease (RP-SLE-ILD) with neuropsychiatric involvement and nephritis and improved after intensive combined immunosuppressive therapy. To characterise the HRCT findings of RP-SLE-ILD, we performed a systematic literature review and identified 27 patients with RP-SLE-ILD, including the present case. OP-dominant patterns, defined as OP alone or OP combined with nonspecific interstitial pneumonia, were significantly more frequent than in the chronic reference cohorts (77.8% vs 10.0% or 14.6%). In contrast, isolated nonspecific interstitial pneumonia was significantly less frequent than in the chronic cohorts (3.7% vs 55.0% or 31.5%). These findings suggest that OP-dominant HRCT patterns and lower lung zone consolidation may be recurring radiological features among reported RP-SLE-ILD cases, although their predictive value requires validation in consecutive cohorts.

快速进展的间质性肺病伴系统性红斑狼疮组织肺炎为主的高分辨率计算机断层扫描模式:1例报告和文献复习。
在系统性红斑狼疮(SLE)的肺部累及中,间质性肺疾病(ILD)是一种罕见但临床意义重大的并发症,有致命病例报道为“急性狼疮肺炎”,并与死亡率增加相关。然而,slel - ild仍然没有根据临床病程进行充分的分层,并且尚未建立快速进展(RP) slel - ild的预测因素,包括高分辨率计算机断层扫描(HRCT)模式。我们在此报告一位71岁男性患者,他表现为呼吸困难、发热、全血细胞减少症、抗双链DNA抗体阳性、低补体血症、蛋白尿和神经精神症状。HRCT最初显示双侧实变主要在肺下周区,与组织性肺炎一致,随后迅速扩展并伴有磨玻璃影。他被诊断为RP-SLE-ILD,伴有神经精神受累和肾炎,经强化联合免疫抑制治疗后病情好转。为了描述RP-SLE-ILD的HRCT表现,我们进行了系统的文献回顾,并确定了27例RP-SLE-ILD患者,包括本病例。组织性肺炎(OP)-显性模式,定义为OP单独或OP合并非特异性间质性肺炎(OP+NSIP),明显高于慢性参考队列(77.8% vs 10.0%或14.6%)。相反,孤立性NSIP的发生率明显低于慢性组(3.7% vs 55.0%或31.5%)。这些发现表明,在RP-SLE-ILD病例中,op主导的HRCT模式和下肺区实变可能是反复出现的影像学特征,尽管它们的预测价值需要在连续队列中得到验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.40
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