Autoinflammatory diseases: Mimics of Autoimmunity or part of its spectrum? Case presentation


Autoria(s): KISS, Maria Helena B.; MAGALHAES, Claudia Saad
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Introduction: Autoinflammatory diseases are very rare diseases presenting within a wide clinical spectrum. Recognition of the main clinical features are challenging due to overlapping or mimicking with autoimmune diseases. Discussion: A case series is reviewed to illustrate typical and atypical features and the difficulties of these diagnoses in the low prevalence areas-a typical unrecognized case of familial Mediterranean fever (FMF) in a youngster, an atypical adult case with overlapping of IMF with Behcet disease, and an early presentation of FMF in infant presenting with inflammatory colitis, as well as the overlapping features within the cryopirin diseases spectrum in an 8-year-old boy who presented with systemic onset arthritis. Conclusion: These cases may represent examples of a very puzzling relationship among disorders of innate and adaptive immune systems and inflammation.

Identificador

JOURNAL OF CLINICAL IMMUNOLOGY, v.28, suppl.1, p.S84-S89, 2008

0271-9142

http://producao.usp.br/handle/BDPI/23554

10.1007/s10875-008-9179-2

http://dx.doi.org/10.1007/s10875-008-9179-2

Idioma(s)

eng

Publicador

SPRINGER/PLENUM PUBLISHERS

Relação

Journal of Clinical Immunology

Direitos

closedAccess

Copyright SPRINGER/PLENUM PUBLISHERS

Palavras-Chave #autoinflammatory disorders #Muckle-Wells syndrome #CINCA/NOMID syndrome #familial Mediterranean fever #RECURRENT MULTIFOCAL OSTEOMYELITIS #FAMILIAL-MEDITERRANEAN-FEVER #BEHCETS-DISEASE #MUCKLE-WELLS #ARTICULAR SYNDROME #PERIODIC SYNDROME #GENE #MUTATIONS #PUSTULOSIS #MEFV #Immunology
Tipo

article

original article

publishedVersion