The Case of a Patient with Limited Systemic Sclerosis and Interstitial Lung Disease Overlapping with Systemic Lupus Erythematosus

K. Krawczyk, E. Mazur, Jaromir Kargol, Robert Kijowski, A. Reich
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引用次数: 0

Abstract

About 20% of patients with systemic sclerosis have symptoms of another connective tissue disease (CTD). Interstitial lung disease (ILD) is one of the most common organ manifestations in systemic sclerosis (SSc) as well as viral illnesses, such as COVID-19, and can lead not only to diffuse alveolar damage, but also trigger an exacerbation of fibrosis among patients with preexisting ILD. It is also associated with substantial morbidity and mortality. According to the World Scleroderma Foundation, SSc-ILD can mask or mimic early COVID-19 lesions and there are no available computed tomography guidelines on how to discern those two conditions. We present a case of systemic sclerosis exacerbation after COVID-19 in a patient with SSc-Lupus Overlap Syndrome.
局限性系统性硬化症、间质性肺病合并系统性红斑狼疮1例
大约20%的系统性硬化症患者有另一种结缔组织疾病(CTD)的症状。间质性肺疾病(ILD)是系统性硬化症(SSc)和病毒性疾病(如COVID-19)中最常见的器官表现之一,不仅可导致弥漫性肺泡损伤,还可引发先前存在ILD的患者纤维化加剧。它还与大量发病率和死亡率有关。根据世界硬皮病基金会的说法,SSc-ILD可以掩盖或模拟早期COVID-19病变,并且没有关于如何区分这两种情况的可用计算机断层扫描指南。我们报告了一例ssc -狼疮重叠综合征患者在COVID-19后出现系统性硬化症加重。
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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