Adult - onset Still's disease : A review.

dc.contributor.authorOwlia, Mohammad Bagher
dc.contributor.authorMehrpoor, Golbarg
dc.date.accessioned2013-03-05T05:33:29Z
dc.date.available2013-03-05T05:33:29Z
dc.date.issued2009-05
dc.description.abstractObjective: This article is an attempt to review recent literature regarding pathogenesis and clinical and laboratory findings in adult-onset Still's disease (AOSD). Materials and methods: A search was conducted in PubMed and Ovid for English language publications, using individual or linked search terms "adult-onset Still's disease," "adult Still's disease," "Still's disease," "AOSD," and other related terms, from 1996 to 2009, and the clinically relevant articles were subsequently selected. Results: More than 1000 titles were reviewed by the authors, and the most important concepts were selected from 143 full-text articles. Conclusion: Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology and pathogenesis, usually presenting with high spiking fever accompanied by systemic manifestations. The disease is an entity with heterogeneous pathology; and diverse suggested etiologies, clinical manifestations and prognoses. There is no single diagnostic test for AOSD; rather, the diagnosis is based on a set of criteria, the most important of which are indeed clinical, but they also include paraclinical ones. Treatment aims at both minimizing inflammation and halting disease progression. For the former, nonsteroidal anti-inflammatory drugs have limited efficacy; so glucocorticoids in conjunction with disease-modifying antirheumatic drugs are also used. Novel therapeutic approaches such as anti-tumor necrosis factor blockade and monoclonal antibodies are promising.en_US
dc.identifier.citationOwlia Mohammad Bagher, Mehrpoor Golbarg. Adult - onset Still's disease : A review. Indian Journal of Medical Sciences. 2009 May; 63(5) 207-221.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/145411
dc.language.isoenen_US
dc.source.urihttps://www.indianjmedsci.org/article.asp?issn=0019-5359;year=2009;volume=63;issue=5;spage=207;epage=221;aulast=Owliaen_US
dc.subjectAdult-onset Still′s diseaseen_US
dc.subjectadult Still′s diseaseen_US
dc.subjectStill′s diseaseen_US
dc.subject.meshAdult
dc.subject.meshHumans
dc.subject.meshStill's Disease, Adult-Onset --diagnosis
dc.subject.meshStill's Disease, Adult-Onset --physiopathology
dc.subject.meshStill's Disease, Adult-Onset --therapy
dc.titleAdult - onset Still's disease : A review.en_US
dc.typeArticleen_US
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