Results 31 to 40 of about 103,363 (247)
Fever and erythema: exclude all and then… think of Still’s disease!
Adult-onset Still’s disease is a rare disease. Diagnosis of Still’s disease is often difficult to achieve. Herein, we describe our diagnostic approach in a case report regarding an adult patient who presented with fever, erythema, lymphadenopathy and ...
Marta Maset +5 more
doaj +1 more source
Background Hyperinflammation with dysregulated production of galectins and cytokines may develop in COVID-19 or adult-onset Still’s disease (AOSD). Given the similar clinical features in both diseases, it is necessary to identify biomarkers that can ...
Po‐Ku Chen +7 more
semanticscholar +1 more source
Background Germinal center kinase-like kinase (GLK, also termed MAP4K3), a member of the MAP4K family, may regulate gene transcription, apoptosis and immune inflammation in response to extracellular signals.
Chen Der-Yuan +6 more
doaj +1 more source
Adult-onset Still's disease (AOSD) is an uncommon systemic auto-inflammatory disease. It can affect multiple body organs. Herein, we report the reproductive hormone and semen profiles in a male with AOSD. A 23-year-old male with already diagnosed and controlled AOSD requested a premarital check-up on his fertility potential.
Salama,Nader, Blgozah,Saeed
openaire +4 more sources
Supplementary methods and Figures S1â S5. (DOCX 2226 kb)
Hu, Qiongyi +16 more
openaire +1 more source
Tofacitinib in refractory adult-onset Still’s disease: 14 cases from a single centre in China
Adult-onset Still’s disease (AOSD) is an autoinflammatory disease characterised by spiking fever, rash, polyarthralgia, sore throat and even life-threatening complications, such as macrophage activation syndrome and fulminant hepatitis.
Qiong-yi Hu +16 more
semanticscholar +1 more source
Adult Onset Still's Disease and Rocky Mountain Spotted Fever
Adult Still's Disease was first described in 1971 by Bywaters in fourteen adult female patients who presented with symptoms indistinguishable from that of classic childhood Still's Disease (Bywaters, 1971).
Paul Persad +2 more
doaj +1 more source
Correlations between inflammatory cell grading (CD4/CD8/CD68 staining) and the percentages of inflammatory cells staining for C-X-C motif chemokine 10 (CXCL10)/C-X-C chemokine receptor type 3 (CXCR3) /CXCL13. Spearmanâ s correlations were calculated. (PPTX 45 kb)
Han, Jae +6 more
openaire +1 more source
We report a series of 3 Adult-onset Still’s disease (AOSD)-like presentations in previously healthy females following vaccination with the ChAdOx1 nCoV-19 vaccine, and also compare them with similar cases reported in literature through a PubMed database ...
Shivraj Padiyar +7 more
semanticscholar +1 more source
Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?
The adult onset Still’s Disease is an uncommon entity characterized by multiple clinical manifestations. Pneumonitis, less often considered, deserves particular emphasis given the need for differential diagnosis and because it can progress to severe ...
Silvia Fernandes +3 more
doaj +1 more source

