Results 1 to 10 of about 103,363 (247)

Adult-onset Still’s disease with dermatomyositis-like lesions [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine
Still’s disease is an inflammatory disorder of unknown origin, also known as juvenile idiopathic arthritis, that predominantly affects children, as it usually appears before the age of 16. However, there is another presentation known as adult-onset Still’
Inés Segovia Rodríguez   +6 more
doaj   +2 more sources

Septic arthritis or adult-onset still’s disease: analyzing the causes of recurrent fever after arthroscopic combined anterior cruciate ligament and posterior cruciate ligament reconstruction: a case report [PDF]

open access: yesBMC Musculoskeletal Disorders
Background Adult-onset still’s disease and septic arthritis share similar symptoms—fever, joint pain, and limited mobility—making postoperative diagnosis difficult after combined anterior cruciate ligament and posterior cruciate ligament reconstruction ...
Zenan Tian   +11 more
doaj   +2 more sources

Macrophage activation syndrome complicating early course of adult-onset Still’s disease [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2021
Introduction. Adult-onset Still’s disease is a rare inflammatory disorder of unknown etiology. It can be complicated by macrophage activation syndrome, a potentially life-threatening condition. While macrophage activation syndrome and adult-onset Still’s
Božić Ksenija   +2 more
doaj   +1 more source

Still’s disease continuum from childhood to elderly: data from the international AIDA Network Still’s disease registry

open access: yesRMD Open, 2023
Objective Still’s disease is more frequently observed in the paediatric context, but a delayed onset is not exceptional both in the adulthood and in the elderly.
Micol Frassi   +75 more
doaj   +1 more source

Adult Still’s disease – a multidisciplinary disease [PDF]

open access: yesArchives of the Balkan Medical Union, 2021
Introduction. Adult-onset Still’s disease is a rare systemic autoinflammatory disorder of unknown etiology, characterized by persistent fever, maculopapular skin rash, and arthritis or arthralgia.
Leonid I. DVORETSKY   +6 more
doaj   +1 more source

Adult-onset Still’s Disease: A Case Report

open access: yesJournal of Nepal Medical Association, 2023
Pyrexia of unknown origin refers to a fever of over 38.3°C on multiple occasions for at least three weeks without a known aetiology, even after a week of hospitalization.
Bikash Karki   +4 more
doaj   +1 more source

Oral mucosa lesions as atypical manifestation of adult-onset Still´s disease [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2018
: Adult-onset Still's disease is a systemic inflammatory disorder of unknown etiology, characterized by skin rash, spiking fever, arthralgias or arthritis, and leukocytosis. The typical skin rash is evanescent, salmon-pink, nonpruritic and maculopapular,
María Lorena Brance, Eldo Luis Neffen
doaj   +1 more source

Management of adult-onset Still's disease: evidence- and consensus-based recommendations by experts

open access: yesRheumatology, 2023
Objectives Adult-onset Still’s disease (AOSD) is a rare condition characterized by fevers, rash, and arthralgia/arthritis; most doctors treating AOSD in the Netherlands treat
H. Leavis   +19 more
semanticscholar   +1 more source

JAK inhibitors in difficult-to-treat adult-onset Still's disease and systemic-onset juvenile idiopathic arthritis.

open access: yesRheumatology, 2022
OBJECTIVES Excessive and inappropriate production of pro-inflammatory cytokines plays a key role in Still's disease. JAK inhibitor (JAKi) agents mainly block pro-inflammatory cytokine pathways, notably IL-6 and IFN.
Louise Gillard   +10 more
semanticscholar   +1 more source

Elderly-onset adult Still’s disease

open access: yesRheumatology, 2021
Adult-onset Still’s disease is a rare inflammatory disorder usually affecting young adults. Elderly-onset Still’s disease (EOSD) is reported in some cases, commonly in Japan, the USA and Europe.
Anis Mzabi   +7 more
doaj   +1 more source

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