Juvenile idiopathic arthritis in Harlequin ichthyosis, a rare combination or the clinical spectrum of the disease? Report of a child treated with etanercept and review of the literature

Harlequin ichthyosis (HI) is the most severe phenotype of autosomal recessive congenital ichthyosis. Juvenile Idiopathic Arthritis (JIA) represents a heterogenous group of disorders all sharing the clinical manifestation of chronic arthritis. Association of HI and chronic arthritis has been reported...

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Veröffentlicht in:Pediatric Rheumatology 2021-06, Vol.19 (1), p.80-80, Article 80
Hauptverfasser: Baldo, Francesco, Brena, Michela, Carbogno, Simone, Minoia, Francesca, Lanni, Stefano, Guez, Sophie, Petaccia, Antonella, Agostoni, Carlo, Cimaz, Rolando, Filocamo, Giovanni
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Sprache:eng
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Zusammenfassung:Harlequin ichthyosis (HI) is the most severe phenotype of autosomal recessive congenital ichthyosis. Juvenile Idiopathic Arthritis (JIA) represents a heterogenous group of disorders all sharing the clinical manifestation of chronic arthritis. Association of HI and chronic arthritis has been reported in few cases. We report the case of a child with HI who developed a severe form of chronic polyarthritis during the first years of life, treated with repeated multiple joint injections, methotrexate and etanercept with good response and without any adverse events. The reported case and the literature review highlighted the presence of a peculiar severe seronegative polyarthritis with early onset in a series of patients with HI, suggesting that polyarthritis may be a specific manifestation of HI, rather than a rare combination of two separate conditions.
ISSN:1546-0096
1546-0096
DOI:10.1186/s12969-021-00571-9