Results 11 to 20 of about 6,693,194 (256)
Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?
Acta 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
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Biomarkers for adult-onset Still’s disease [PDF]
Научно-практическая ревматология, 2022 Adult-onset Still’s disease (AOSD) is a rare complex autoinflammatory disease of unknown etiology. The main problem, practitioners have been facing with when researching AOSD, is the lack of developed approaches to assessing the activity of the disease ...
V. Yu. Myachikova +4 more
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Association between adult-onset still’s disease and COVID-19: A report of two cases and brief review
SAGE Open Medical Case ReportsAdult-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
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Hepatic tuberculosis presenting with extreme hyperferritinemia masquerading as adult-onset Still’s disease: a case report [PDF]
Journal 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
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Macrophage Activation Syndrome Associated with Adult-Onset Still’s Disease Successfully Treated with Anakinra [PDF]
Case 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
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Journal 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
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Adult Onset Still’s Disease: A Case Report with a Rare Clinical Manifestation and Pathophysiological Correlations [PDF]
Case Reports in Medicine, 2013 Adult-onset Still’s disease is an inflammatory multisystemic disease of unknown etiology. Pleuritis is the most common pulmonary manifestation and pleural effusions are usually exudates with a predominance of neutrophils.
Katerina M. Antoniou +6 more
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Apollo Medicine, 2010 Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disorder characterised by high spiking fever, an evanescent salmon pink rash and arthritis,frequently accompanied by sore throat, myalgias, lymphadenopathies, splenomegaly and ...
Lalitha Sekhar +3 more
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Adult Onset Still’s Disease in Oman [PDF]
Sultan Qaboos University Medical Journal, 2006 Objective: To 1. Highlight the demographic characteristics, clinical features, laboratory investigations and outcome if possible of a relatively rare disease (Adult Onset Still’s Disease {AOSD}) and 2.
Faisal A Al-Temimi, Prasad George
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Acute Myocarditis Revealing Adult-Onset Still’s Disease
, 2021 International audienceA 34-year-old man presented with fever, palpitations, maculopapular rash, pharyngitis, left cheilitis, and bilateral gonalgia. High-sensitivity troponin I concentration was 4,900 ng/l.
Ederhy, Stéphane +8 more
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