Results 11 to 20 of about 4,864,129 (252)

Macrophage Activation Syndrome Associated with Adult-Onset Still’s Disease Successfully Treated with Anakinra [PDF]

open access: yesCase Reports in Rheumatology, 2016
Macrophage activation syndrome (MAS) is a potentially fatal complication of Adult-Onset Still’s disease (Still’s disease). Whereas an increasing body of evidence supports interleukin-1 (IL-1) blockade as a promising treatment for Still’s disease, whether
Aswini Kumar, Hiroshi Kato
doaj   +2 more sources

ADULT-ONSET STILL’S DISEASE: ASPECTS OF THE HEMATOLOGY CLINIC

open access: yesСибирский научный медицинский журнал, 2019
The analysis of literature data on modern approaches in the diagnosis and treatment of adult-onset Still’s disease has been performed. A clinical case of Still’s disease associated with lymphadenopathy syndrome was demonstrated.
M. M. Agakishiev   +6 more
doaj   +2 more sources

Fever and erythema: exclude all and then… think of Still’s disease!

open access: yesItalian Journal of Medicine, 2016
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   +2 more sources

Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?

open access: yesActa Médica Portuguesa, 2017
The adult onset Still’s Disease is an uncommon entity characterized by multiple clinical manifestations. Pneumonitis, less often considered, deserves particular emphasis given the need for differential diagnosis and because it can progress to severe ...
Silvia Fernandes   +3 more
doaj   +2 more sources

Association between adult-onset still’s disease and COVID-19: A report of two cases and brief review

open access: yesSAGE Open Medical Case Reports
Adult-onset still’s disease is a rare multisystemic autoinflammatory disorder with an estimated annual incidence of 0.16–0.62 per 100,000 individuals worldwide. It is typically considered a diagnosis of exclusion.
Sarah Fet-He   +2 more
doaj   +2 more sources

Adult Still’s disease and Tako-Tsubo syndrome [PDF]

open access: yesClinical Management Issues, 2012
Here we describe the case of a 68-year-old Italian female who was admitted in our hospital for the occurrence of arthralgia, abdominal pain and general discomfort.
Susanna Cozzio   +4 more
doaj   +2 more sources

Efficacy of canakinumab in patients with Still’s disease across different lines of biologic therapy: real-life data from the International AIDA Network Registry for Still’s Disease [PDF]

open access: yesFrontiers in Medicine, 2023
IntroductionThe effectiveness of canakinumab may change according to the different times it is used after Still’s disease onset. This study aimed to investigate whether canakinumab (CAN) shows differences in short- and long-term therapeutic outcomes ...
Antonio Vitale   +75 more
doaj   +2 more sources

Elevated serum levels of interleukin-18 discriminate Still’s disease from other autoinflammatory conditions: results from the European ImmunAID cohort

open access: yesRMD Open
Objectives Systemic autoinflammatory diseases (SAIDs) represent a set of conditions with exaggerated innate immune responses. IL-1β and IL-18 are key cytokines involved in the pathogenesis of some SAID.
  +94 more
doaj   +2 more sources

Hepatic tuberculosis presenting with extreme hyperferritinemia masquerading as adult-onset Still’s disease: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2012
Introduction Isolated hepatic tuberculosis is an uncommon manifestation of one of the most common infections worldwide, caused by Mycobacterium tuberculosis. Extremely high serum ferritin, which is regarded as a marker of adult onset Still’s disease, has
Manoj Edirisooriya   +2 more
doaj   +2 more sources

Noncaseating suppurative granulomatous lymphadenitis in adult onset Still’s disease – a diagnostic dilemma in a tuberculosis-endemic region: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Lymphadenopathy is not an uncommon presentation of adult onset Still’s disease: it is present in up to two thirds of patients with adult onset Still’s disease.
S. W. G. J. W. Chinthaka   +5 more
doaj   +2 more sources

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