Results 21 to 30 of about 118,654 (333)

Recurring Lower Abdominal Pain and Fever as Initial Presentation of Adult Onset Still’s Disease in the Absence of Arthralgia and Other System Involvement [PDF]

, 2017
A 34 year-old Afro-Caribbean female presented with recurring episodes of fever and lower abdominal pain over a period of two months not improving despite courses of antibiotics for possible recurrent urinary tract infections.
Rajaiah, Nithyananda, Saim, Mohammad, Sreh, Abuajela   +2 more
core   +7 more sources

Adult-Onset Still’s Disease—A Complex Disease, a Challenging Treatment

International Journal of Molecular Sciences, 2022
Adult-onset Still’s disease (AOSD) is a systemic inflammatory disorder with an unknown cause characterized by high-spiking fever, lymphadenopathy, hepatosplenomegaly, hyperferritinemia, and leukocytosis.
L. Macovei, A. Burlui, I. Bratoiu, C. Rezus, A. Cardoneanu, P. Richter, A. Szalontay, E. Rezuș   +7 more
semanticscholar   +1 more source

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

Rheumatology, 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, Paul L. A. van Daele, C. Mulders-Manders, R. Michels, A. Rutgers, E. Legger, M. Bijl, E. Hak, Wai‐Kwan Lam‐Tse, F. Bonte‐Mineur, Peter Fretter, Anna Simon, P. van Paassen, Marlies van der Goes, M. Flendrie, W. Vercoutere, A. W. V. van Lieshout, Arjen P. Leek, S. Vastert, S. Tas   +19 more
semanticscholar   +1 more source

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

Rheumatology, 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, J. Pouchot, F. Cohen-Aubart, I. Koné-Paut, G. Mouterde, M. Michaud, H. Reumaux, L. Savey, A. Belot, B. Fautrel, S. Mitrovic   +10 more
semanticscholar   +1 more source

Elderly-onset adult Still’s disease

Rheumatology, 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, Rym Fakhfakh, Maissa Thabet, Imen Ben Hassine, Jihed Anoun, Monia Karmani, Fatma Ben Fredj, Chadia Laouani   +7 more
doaj   +1 more source

Refractory Adult Onset Still’s Disease [PDF]

Cureus, 2017
It is often a challenge and a dilemma for clinicians encountering patients with pyrexia of unknown origin. Numerous tests performed to determine the underlying cause often give inconclusive results. We present a 52-year-old man with undulating fever for more than 10 months with persistent hyperferritinaemia, and negative immunological and serological ...
Sulaiman, Wahinuddin, Abdullah, Aris Chandran, Tan Tsen Chuen, Jerome, Baba, Shaffie, Karim, Norain   +4 more
openaire   +2 more sources

Adult-Onset Still Disease (AOSD) [PDF]

The Journal of the American Board of Family Medicine, 2010
Adult-onset Still disease (AOSD) is an uncommon clinical entity that predominantly affects young adults. One of the most common presentations of the disease is fever of unknown origin. Early diagnosis can be difficult because fever of unknown origin is more commonly seen with other conditions such as malignancy or infection.
Egambaram, Senthilvel, Aphrodite, Papadakis, Michael, McNamara, Iyabode, Adebambo   +3 more
openaire   +2 more sources

The association between adult-onset Still’s disease and collapsing glomerulopathy: a case report

Journal of Medical Case Reports, 2022
Background Collapsing glomerulopathy, characterized by marked hypertrophy and hyperplasia of the podocytes with eventual collapse of the glomerular tuft, is an important cause of end-stage renal disease. Among the many causes of collapsing glomerulopathy,
Matas Orentas, Nilam Patel, Roger Rodby, Sobia Hassan   +3 more
doaj   +1 more source

Treatment of adult-onset Still's disease: a review [PDF]

, 2014
Adult-onset Still's disease (AOSD) is a rare inflammatory disorder that has been recently classified as a polygenic autoinflammatory disorder. The former classification, based on the disease course, seems to be quite dated.
Gerfaud-Valentin, M., Henry, T., Jamilloux, Y., Seve, P.   +3 more
core   +3 more sources

Adult-Onset Still’s Disease: Clinical Aspects and Therapeutic Approach

Journal of Clinical Medicine, 2021
Adult-onset Still’s disease (AoSD) is a rare systemic autoinflammatory disease characterized by arthritis, spiking fever, skin rash and elevated ferritin levels.
Stylianos Tomaras, Carl Christoph Goetzke, T. Kallinich, E. Feist   +3 more
semanticscholar   +1 more source