Lung lesion in a patient with systemic lupus erythematosus

E. Pravkina, A. S. Baranova, S. P. Filonenko, S. A. Molchanov
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Abstract

Systemic lupus erythematosus is a chronic rheumatic autoimmune disease characterized by polysystemic lesions and a variety of clinical manifestations. This disease often aff ects the respiratory system, represented mainly by pleurisy or pulmonary hypertension. However, this publication describes a clinical case in which lung damage in a patient who has had systemic lupus erythematosus for over than 25 years, manifested itself as interstitial lung disease (ILD), which is more typical for other rheumatic diseases, such as  diff use scleroderma, Sjogren disease. ILD manifested with an atypically bright clinical picture, progressed and required the prescription of genetically engineered biological drugs. Their use was complicated by recurrent urinary tract infection, and therefore these drugs were withheld. A peculiar feature of ILD is its blurred clinical picture, which causes additional diffi  culties in diff erential diagnosis, especially during the period of widespread new coronavirus infection, taking into account similar clinical manifestations and changes detected by computed tomography of the lungs, so it leads to a late start of pathogenetic therapy. In this regard, the episode of recrudescence of the patient’s condition manifested by a clinical picture and a pattern of changes on a CT scan, similar to both progressive IPL and pneumonia associated with a new coronavirus infection, which complicated diff erential diagnosis and management tactics, deserves special attention.
系统性红斑狼疮患者肺部病变
系统性红斑狼疮是一种慢性风湿性自身免疫性疾病,以多系统病变和多种临床表现为特征。本病常累及呼吸系统,主要表现为胸膜炎或肺动脉高压。然而,本出版物描述了一个临床病例,患者患有系统性红斑狼疮超过25年,肺损伤表现为间质性肺疾病(ILD),这是更典型的其他风湿性疾病,如硬皮病,干燥病。ILD表现为非典型的临床表现,病情进展,需要使用基因工程生物药物。他们的使用是复杂的复发性尿路感染,因此这些药物被扣留。ILD的一个特点是其模糊的临床表现,这给鉴别诊断带来了额外的困难,特别是在新型冠状病毒广泛感染期间,考虑到肺部计算机断层扫描检测到的相似临床表现和变化,因此导致发病治疗开始较晚。因此,临床表现和CT扫描改变模式显示的患者病情复发的发作,类似于进行性IPL和新型冠状病毒感染相关肺炎,这给鉴别诊断和治疗策略带来了复杂的问题,值得特别关注。
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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