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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
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Adult-onset Still's Disease: A Case Report
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
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Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report
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
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A case of adult‐onset Still's disease in a patient after a car accident
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
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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
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Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report
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
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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
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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
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Supplementary methods and Figures S1â S5. (DOCX 2226 kb)
Hu, Qiongyi +16 more
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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
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