Adult‐onset Still's disease after SARS‐Cov‐2 infection

Adult‐onset Still's disease (AOSD) is an uncommon inflammatory disorder. AOSD and SARS‐Cov‐2 infection share clinical and laboratory features, including systemic inflammation. A 19‐year‐old woman had prolonged fever for 3 weeks, joint pain, and biological inflammatory syndrome. Post COVID‐19 AOSD was diagnosed. SARS‐Cov‐2 infection induces many inflammatory diseases including AOSD.

[1]  H. Maecker.  Immune profiling of COVID-19: preliminary findings and implications for the pandemic , 2021, Journal for ImmunoTherapy of Cancer.

[2]  M. Hallek,et al.  First manifestation of adult-onset Still's disease after COVID-19 , 2021, The Lancet Rheumatology.

[3]  F. Montorsi,et al.  Interleukin-1 and interleukin-6 inhibition compared with standard management in patients with COVID-19 and hyperinflammation: a cohort study , 2021, The Lancet Rheumatology.

[4]  Mohammed Samannodi,et al.  Diagnosis of Adult Onset Still’s Disease in a Patient Who has recovered from Coronavirus-19 , 2021, Clinical medicine insights. Case reports.

[5]  J. D. de Carvalho.  COVID-19 in Still's disease. , 2020, European review for medical and pharmacological sciences.

[6]  Hongyang Wang,et al.  Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing , 2020, Cell Discovery.

[7]  Hongyang Wang,et al.  Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing , 2020, Cell Discovery.

[8]  Z. Memish,et al.  The continuing 2019-nCoV epidemic threat of novel coronaviruses to global health — The latest 2019 novel coronavirus outbreak in Wuhan, China , 2020, International Journal of Infectious Diseases.

[9]  N. Quan,et al.  Salient type 1 interleukin 1 receptor expression in peripheral non-immune cells , 2018, Scientific Reports.

[10]  P. Efthimiou,et al.  Adult-Onset Still’s Disease , 2012, Drugs.

[11]  A. Prost,et al.  Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west France. , 1995, Annals of the rheumatic diseases.

[12]  M. Akizuki,et al.  Preliminary criteria for classification of adult Still's disease. , 1992, The Journal of rheumatology.

[13]  J. Esdaile,et al.  Adult Still's Disease: Manifestations, Disease Course, and Outcome in 62 Patients , 1991, Medicine.