Journal of Clinical Immunology

, Volume 28, Supplement 1, pp 73–83

Diagnosis and Management of Autoinflammatory Diseases in Childhood

Authors

    • 2nd Division of Pediatrics, “G. Gaslini” Scientific Institute
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Silvia Federici
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Maria Antonietta Pelagatti
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Roberta Caorsi
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Giacomo Brisca
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Clara Malattia
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
  • Alberto Martini
    • 2nd Division of Pediatrics, “G. Gaslini” Institute and Laboratory of Immunology of Rheumatic Diseases, Department of PediatricsUniversity of Genoa
Article

DOI: 10.1007/s10875-008-9178-3

Cite this article as:
Gattorno, M., Federici, S., Pelagatti, M.A. et al. J Clin Immunol (2008) 28: 73. doi:10.1007/s10875-008-9178-3

Abstract

Introduction

Autoinflammatory diseases are a group monogenic inflammatory conditions characterized by an early onset during childhood.

Discussion

Under the term “periodic fevers” are gathered some monogenic diseases (familial Mediterranean fever, mevalonate kinase deficiency, and tumor necrosis factor receptor-associated syndrome) characterized by periodic or recurrent episodes of systemic inflammation causing fever often associated with rash, serositis (peritonitis, pleuritis), lymphadenopathy, arthritis, and other clinical manifestations. Systemic reactive (AA) amyloidosis may be a severe long-term complication. Cryopyrinopathies are a group of conditions associated to mutations of the gene Cryopyrin that are responsible for a spectrum of diseases (familial cold autoinflammatory syndrome, Muckle–Wells syndrome, and chronic infantile neurological cutaneous and articular syndrome) characterized by a chronic or recurrent systemic inflammation variably associated with a number of clinical features, such as urticarial-like rash, arthritis, sensorineural deafness, and central nervous system and bone involvement. Other disorders are dominated by the presence of sterile pyogen abscesses prevalently affecting the skin, joints, and bones (pyogenic disorders). These include pyogenic sterile arthritis, pyoderma gangrenosum, and acne syndrome, and Majeed syndrome. Finally, some diseases, such as Blau’s syndrome, are characterized by the appearance of typical noncaseating granulomatous inflammation affecting the joints, skin, and uveal tract (granulomatous disorders). In the present review, we will focus on the clinical presentation of these disorders in childhood and report on the available therapeutic strategies.

Keywords

Familial Mediterranean fevermevalonate kinase deficiencytumor necrosis factor (TNF) receptor-associated syndromecryopyrinopathies

Copyright information

© Springer Science+Business Media, LLC 2008