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Adult-onset Still’s disease is a rare inflammatory disorder characterised by fever, arthritis and rash. It can present in a number of ways and is associated in 5% of cases with parenchymal lung involvement.
Robert Perry +4 more
doaj +1 more source
Case Report of a Female Patient with Adult-onset Still's Disease and Review of the Literature [PDF]
Background: Adult-onset Still's disease (AOSD), which presents many non-specific symptoms, such as rash leukocytosis, spiking fever, and sore throat, is a rare auto inflammatory disease.
Yan Gao +4 more
doaj +1 more source
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
Adult‐onset Still's disease complicated by macrophage activation syndrome
Key Clinical Message Young patients with persistent rash and fevers despite antibiotic treatment should be evaluated for non‐infectious etiologies. In our patient's case, these findings led to a diagnosis of MAS, which ultimately affected how she was ...
Toluwalase Awoyemi +2 more
doaj +1 more source
Anakinra in children and adults with Still’s disease [PDF]
AbstractSystemic juvenile idiopathic arthritis and adult-onset Still’s disease are rare autoinflammatory disorders with common features, supporting the recognition of these being one disease—Still’s disease—with different ages of onset. Anakinra was recently approved by the European Medicines Agency for Still’s disease.
Vastert, Sebastiaan +8 more
openaire +3 more sources
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
doaj +1 more source
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
doaj +1 more source
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
doaj +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
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
doaj +1 more source

