| Literature DB >> 29860887 |
Bernadett Mosdósi1, Beáta Tóth2.
Abstract
Autoinflammatory diseases are disorders of the innate immune system characterized by recurrent systematic inflammation and serious complications. Dysregulation of inflammasome and overproduction of interleukin-1 play a major role in the pathogenesis of autoinflammatory diseases. The diagnosis of these rare conditions rely on recognising the pattern of presentation and differential diagnosis. Manifestations may include fever, rash, serositis (pleuritis and peritonitis), arthritis, meningitis and uveitis. Secondary amyloidosis may complicate longstanding disease. Advances in our understanding of the molecular and pathophysiological basis of the autoinflammatory diseases have resulted in new treatment strategies. Early diagnosis and effective therapy are critical to prevent irreversible organ damage. The purpose of this review is to describe the major clinical, genetic, and therapeutic features of the most common autoinflammatory syndromes. Orv Hetil. 2018; 159(23): 898-907.Entities:
Keywords: autoinflammatiós kórképek; autoinflammatory disorders; fever; inflammasoma; inflammasome; interleukin-1; láz
Mesh:
Year: 2018 PMID: 29860887 DOI: 10.1556/650.2018.31068
Source DB: PubMed Journal: Orv Hetil ISSN: 0030-6002 Impact factor: 0.540