The first case of SARS-CoV-2-induced eosinophilic fasciitis.

IF 0.9 Q4 RHEUMATOLOGY
Hiba Boussaa, Mariem Kamoun, Saoussen Miladi, Yasmine Makhlouf, Kawther Ben Abdelghani, Alia Fazaa, Ahmed Laatar
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Abstract

Eosinophilic fasciitis (EF), also known as Shulman syndrome, is a rare auto-immune fibrosing disorder of the fascia. Etiopathogeny of EF is still unclear. Nowadays, it is widely known that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may induce hyper-stimulation of the immune system. Several cases with fasciitis and rhabdomyolysis induced by coronavirus disease 2019 vaccines have been reported in the literature. Herein, we report the first case of EF possibly triggered by SARS-CoV-2 infection. A 45-year-old Tunisian woman, with no medical history, presented to our department with severe widespread muscle pain noticed one month after a SARS-CoV-2 infection. Physical examination showed an induration of the skin and subcutaneous tissue of the arms, forearms and legs with a restricted joint mobility. The level of eosinophils was 430 E/mm3 (6.1%) [1-4%]. Electromyography and creatine kinase levels were normal. Myositis-related antibodies were negative. Magnetic resonance imaging of the left arm showed high-intensity signal and thickness of the fascia without evidence of muscle or bone involvement. A muscular biopsy from the right deltoid showed thickening and inflammation of the fascia. The patient received intraveinous injections of 1000 mg of methylprednisolone for 3 days with an oral relay of 1 mg/kg per day of prednisone equivalent during 4 weeks. At one-month follow-up, a significant improvement of the skin induration and myalgia was observed, with a disappearance of the biological inflammatory syndrome. This brief report suggests a potential link between SARS-CoV-2 infection and new-onset of auto-immune fasciitis.

首例严重急性呼吸系统综合征冠状病毒2型引起的嗜酸性筋膜炎。
嗜酸性筋膜炎(EF),也称为舒尔曼综合征,是一种罕见的筋膜自身免疫纤维化疾病。EF的病因尚不清楚。如今,众所周知,严重急性呼吸系统综合征冠状病毒2型可能会诱导免疫系统的过度刺激。文献中报道了几例新冠肺炎疫苗诱导的筋膜炎和横纹肌溶解症。在此,我们报告了第一例可能由严重急性呼吸系统综合征冠状病毒2型感染引发的EF病例。一名45岁的突尼斯妇女,无病史,在感染严重急性呼吸系统综合征冠状病毒2型一个月后,出现严重的广泛肌肉疼痛。体格检查显示,手臂、前臂和腿的皮肤和皮下组织硬结,关节活动受限。嗜酸性粒细胞水平为430 E/mm3(6.1%)[1-4%]。肌电图和肌酸激酶水平正常。肌炎相关抗体为阴性。左臂的磁共振成像显示高强度信号和筋膜厚度,没有肌肉或骨骼受累的证据。右侧三角肌的肌肉活检显示筋膜增厚和炎症。患者接受1000 mg甲基强的松龙静脉注射3天,并在四周内每天口服1 mg/kg的强的松酮当量。在一个月的随访中,观察到皮肤硬结和肌痛的显著改善,生物炎症综合征消失。这份简短的报告表明,严重急性呼吸系统综合征冠状病毒2型感染与新发的自身免疫性筋膜炎之间存在潜在联系。
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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