Results 21 to 30 of about 6,693,207 (250)

Acute Myocarditis Revealing Adult-Onset Still’s Disease

open access: yes, 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
core   +1 more source

Canakinumab injection for the treatment of active Still’s disease, including adult-onset Still’s disease

open access: yes, 2021
Introduction: Still’s disease is a systemic, non-monogenic autoinflammatory condition affecting both children and adolescents (systemic juvenile idiopathic arthritis, sJIA) and adults (adult-onset Still’s disease, AOSD). Its clinical spectrum ranges from
Campochiaro C.   +5 more
core   +1 more source

Adult-onset Still's Disease: A Case Report

open access: yesJournal of Nepal Medical Association, 2020
Adult-onset Still’s Disease is a rare auto inflammatory disorder of unknown etiology characterized mainly by high spiking fever, arthritis, evanescent rash and lymphadenopathy.
Ashok Sapkota   +4 more
doaj   +1 more source

Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Adult onset Still's disease is a chronic multisystemic inflammatory disorder characterized by high spiking fever, polyarthralgia and rash.
Otrock Zaher K   +5 more
doaj   +1 more source

Adult-Onset Still’s Disease Presenting as Macrophage-Activation Syndrome With Critical Illness in the Third Trimester of Pregnancy: A Case Report

open access: yesCritical Care Explorations, 2021
BACKGROUND:. We report a case of a young woman with adult-onset Still’s disease presenting as macrophage-activation syndrome complicated by shock and respiratory failure during the third trimester of pregnancy. CASE SUMMARY:. A previously healthy 26-year-
Andrew T. Peters, MD   +1 more
doaj   +1 more source

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

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

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

CHARACTERISTICS OF ADULT-ONSET STILL’S DISEASE IN THE 21ST CENTURY [PDF]

open access: yes, 2018
The review gives an update on adult-onset Still’s disease: on its causes, the specific features of its pathogenesis, diagnosis, clinical presentations (with identification of subtypes), and treatment with consideration for the nature of the course of the
V. V. Lebedeva, Yu. V. Muravyev
core   +1 more source

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