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Adult-onset Still's disease with atypical cutaneous manifestations [PDF]
, 2018 The diagnosis of adult-onset Still's disease (AOSD) can be very difficult. There are no specific tests available, and diagnosis is usually based on a symptom complex and the well-described typical evanescent rash seen in the majority of patients. However,
Juarez, Pablo +6 more
core +1 more source
Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report
Journal 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
Macrophage Activation Syndrome [PDF]
, 2015 Macrophage activation syndrome (MAS) is a potentially life-threatening complication of rheumatic diseases such as systemic juvenile idiopathic arthritis (sJIA) and systemic lupus erythematosus.
Clarke, Sarah L N +2 more
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Adult-onset Still's Disease: A Case Report
Journal 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
A case of adult‐onset Still's disease in a patient after a car accident
Clinical 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
Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome [PDF]
, 1994 Contains fulltext : 4767.pdf (publisher's version ) (Open ...
Boom, B.W. +3 more
core +2 more sources
Elevated Troponin Serum Levels in Adult Onset Still's Disease [PDF]
, 2015 Adult onset Still's disease (AOSD) is a rare inflammatory systemic disease that occasionally may affect myocardium. Diagnosis is based on typical AOSD symptoms after the exclusion of well-known infectious, neoplastic, or autoimmune/autoinflammatory ...
Brugioni, Lucio +7 more
core +3 more sources
Autoimmunity Reviews, 2014 First described in 1971, adult-onset Still's disease (AOSD) is a rare multisystemic disorder considered as a complex (multigenic) autoinflammatory syndrome. A genetic background would confer susceptibility to the development of autoinflammatory reactions to environmental triggers.
Gerfaud-Valentin, Mathieu +3 more
openaire +4 more sources
BMC Medicine, 2012 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