Results 21 to 30 of about 6,693,194 (256)

Canakinumab injection for the treatment of active Still’s disease, including adult-onset Still’s disease

open access: yes, 2021
Introduction: Still’s disease is a systemic, non-monogenic autoinflammatory condition affecting both children and adolescents (systemic juvenile idiopathic arthritis, sJIA) and adults (adult-onset Still’s disease, AOSD). Its clinical spectrum ranges from
Campochiaro C.   +5 more
core   +1 more source

Adult-onset Still's Disease: A Case Report

open access: yesJournal of Nepal Medical Association, 2020
Adult-onset Still’s Disease is a rare auto inflammatory disorder of unknown etiology characterized mainly by high spiking fever, arthritis, evanescent rash and lymphadenopathy.
Ashok Sapkota   +4 more
doaj   +1 more source

Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Adult onset Still's disease is a chronic multisystemic inflammatory disorder characterized by high spiking fever, polyarthralgia and rash.
Otrock Zaher K   +5 more
doaj   +1 more source

A case of adult‐onset Still's disease in a patient after a car accident

open access: yesClinical Case Reports, 2023
Key Clinical Message Adult‐onset Still's disease is a rare inflammatory condition with diverse clinical features. Yamaguchi criteria aid diagnosis, and pleural effusion and elevated ferritin levels are important markers.
Feride Yaman, Ali Kimiaei
doaj   +1 more source

Additional file 2: of Association of CXCL10 and CXCL13 levels with disease activity and cutaneous manifestation in active adult-onset Stillâ s disease

open access: yes, 2015
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

Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report

open access: yesJournal of Medical Case Reports, 2012
Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F   +5 more
doaj   +1 more source

Association Between Peripheral Eosinophilia and Clinical Characteristics of Adult-onset Still’s Disease with Persistent Eruption: A Retrospective Study

open access: yesActa Dermato-Venereologica, 2021
Persistent eruption occurs in a subset of patients with adult-onset Still’s disease. In our experience, a considerable proportion of these patients present with peripheral eosinophilia.
Jia-Wei Liu   +6 more
doaj   +1 more source

Adult-Onset Still’s Disease Presenting as Macrophage-Activation Syndrome With Critical Illness in the Third Trimester of Pregnancy: A Case Report

open access: yesCritical Care Explorations, 2021
BACKGROUND:. We report a case of a young woman with adult-onset Still’s disease presenting as macrophage-activation syndrome complicated by shock and respiratory failure during the third trimester of pregnancy. CASE SUMMARY:. A previously healthy 26-year-
Andrew T. Peters, MD   +1 more
doaj   +1 more source

Additional file 1: of Increased neutrophil extracellular traps activate NLRP3 and inflammatory macrophages in adult-onset Stillâ s disease

open access: yes, 2019
Supplementary methods and Figures S1â S5. (DOCX 2226 kb)
Hu, Qiongyi   +16 more
openaire   +1 more source

Fever and erythema: exclude all and then… think of Still’s disease!

open access: yesItalian Journal of Medicine, 2016
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

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