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 +2 more
core +7 more sources
Oral mucosa lesions as atypical manifestation of adult-onset Still´s disease [PDF]
Anais Brasileiros de Dermatologia, 2018 : Adult-onset Still's disease is a systemic inflammatory disorder of unknown etiology, characterized by skin rash, spiking fever, arthralgias or arthritis, and leukocytosis. The typical skin rash is evanescent, salmon-pink, nonpruritic and maculopapular,
María Lorena Brance, Eldo Luis Neffen
doaj +1 more source
Rheumatology International, 2009 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 neutrophilic leukocytosis.
Bagnari V +4 more
openaire +4 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 +3 more
doaj +1 more source
Case Report of a Female Patient with Adult-onset Still's Disease and Review of the Literature [PDF]
Iranian Journal of Immunology, 2022 Background: Adult-onset Still's disease (AOSD), which presents many non-specific symptoms, such as rash leukocytosis, spiking fever, and sore throat, is a rare auto inflammatory disease.
Yan Gao +4 more
doaj +1 more source
Therapy with canakinumab for adult-onset still's disease
Научно-практическая ревматология, 2019 Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic ...
E. L. Nasonov
doaj +1 more source
A promoter haplotype of the interleukin-18 gene is associated with juvenile idiopathic arthritis in the Japanese population [PDF]
, 2015 journal ...
HARA, Masako +8 more
core +2 more sources
Fever and erythema: exclude all and then… think of Still’s disease!
Italian 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
Adult‐onset Still's disease complicated by macrophage activation syndrome
Clinical Case Reports, 2023 Key Clinical Message Young patients with persistent rash and fevers despite antibiotic treatment should be evaluated for non‐infectious etiologies. In our patient's case, these findings led to a diagnosis of MAS, which ultimately affected how she was ...
Toluwalase Awoyemi +2 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. +3 more
core +3 more sources