Results 21 to 30 of about 2,676 (234)

A case of adult‐onset Still's disease in a patient after a car accident

open access: yesClinical 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

Biomarkers for adult-onset Still’s disease

open access: yesНаучно-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
doaj   +1 more source

Adult-onset Still’s disease

open access: yesJournal of Medical and Scientific Research, 2015
A 24-year-old male presented with fever, sore throat, and arthralgias for duration of 4 weeks. Fever was high grade, intermittent, associated with maculopapular rash. He was admitted in outside hospital and was started on antibiotics, antituberculosis treatment (ATT), and anti-malarials. The patient was discharged without any improvement.
Srinivas   +2 more
openaire   +4 more sources

Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report

open access: yesJournal 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

Association Between Peripheral Eosinophilia and Clinical Characteristics of Adult-onset Still’s Disease with Persistent Eruption: A Retrospective Study

open access: yesActa Dermato-Venereologica, 2021
Persistent eruption occurs in a subset of patients with adult-onset Still’s disease. In our experience, a considerable proportion of these patients present with peripheral eosinophilia.
Jia-Wei Liu   +6 more
doaj   +1 more source

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   +1 more source

Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still's disease and may act as an activity marker

open access: yesBMC 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

Adult Onset Still's Disease and Rocky Mountain Spotted Fever

open access: yesCase Reports in Medicine, 2010
Adult Still's Disease was first described in 1971 by Bywaters in fourteen adult female patients who presented with symptoms indistinguishable from that of classic childhood Still's Disease (Bywaters, 1971).
Paul Persad   +2 more
doaj   +1 more source

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   +1 more source

ADULT-ONSET STILL'S DISEASE TODAY

open access: yesНаучно-практическая ревматология, 2017
The lecture gives an update on adult-onset Still's disease, including that on the specific features of the clinical picture and treatment of this disease.
Yu. V. Muravyev, V. V. Lebedeva
doaj   +1 more source

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