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| http://dx.doi.org/10.1038/aja.2010.34 | DOI Listing |
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[Interpretation of the EULAR and PReS recommendations for the diagnosis and management of Still's disease, comprising systemic juenile idiopathic arthritis and adult-onset Still's disease].
Zhonghua Er Ke Za Zhi
December 2024
Department of Pediatrics, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Delayed diagnosis of adult onset Still's disease in 2 cases: diagnostic dilemma in positive antinuclear antibody and tuberculosis endemic areas.
Postgrad Med
November 2024
Internal Medicine, Department of Internal Medicine, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Article Synopsis
- Adult-onset Still's disease (AoSD) is a rare inflammatory condition affecting young adults, often misdiagnosed as other diseases.
- Two cases are outlined where AoSD was initially misidentified as tuberculous arthritis and systemic lupus erythematosus (SLE), leading to ineffective treatments.
- After further evaluation, both patients were correctly diagnosed with AoSD and treated with high-dose methylprednisolone and methotrexate, resulting in clinical improvement and reduced ferritin levels.
Characteristics of Patients with Adult-Onset Dermatomyositis at 2 Tertiary Care Centres in Ontario, Canada.
J Cutan Med Surg
November 2024
Michael G. DeGroote School of Medicine, Hamilton, ON, Canada.
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by progressive muscle weakness and distinctive cutaneous findings. The exact incidence and prevalence of DM in the general population is largely unknown, and data on demographic and clinical features in patients in Canada are lacking. This study aimed to comprehensively evaluate the patients with DM in Southwestern Ontario, Canada.
View Article and Find Full Text PDFExploring the Symptoms of and Insights Into Idiopathic Opsoclonus-Myoclonus-Ataxia Syndrome in Adults.
Cureus
October 2024
Neurology, Hospital San Juan de Dios, San José, CRI.
Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare immunological central nervous system disorder that mostly affects children, and it is extremely uncommon in adults. It usually presents idiopathically, as a parainfectious condition, or as a paraneoplastic syndrome. We present a case of a patient who developed adult-onset opsoclonus-myoclonus-ataxia syndrome (OMAS) without any associated infectious or neoplastic disease, a condition that is considered very rare in Central America.
View Article and Find Full Text PDFLifetime clinical presentation of Still's disease in the Afro-descendant population of the French West Indies.
Joint Bone Spine
November 2024
EpiCliV Research Unit, University of the French West Indies, Martinique University Hospital, Fort-de France, Martinique; Department of Internal Medicine, Martinique University Hospital, Fort-de France, Martinique.
Introduction: The continuum in Still's disease has never been addressed in Afro-descendant (AD) populations. The aim of this study was to compare the features of Still's disease between children and adults in the AD population of French West Indies (FWI).
Methods: Retrospective longitudinal study from January 2000-2022.
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