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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.

Authors :
Baldo F
Brena M
Carbogno S
Minoia F
Lanni S
Guez S
Petaccia A
Agostoni C
Cimaz R
Filocamo G
Source :
Pediatric rheumatology online journal [Pediatr Rheumatol Online J] 2021 Jun 03; Vol. 19 (1), pp. 80. Date of Electronic Publication: 2021 Jun 03.
Publication Year :
2021

Abstract

Background: 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.<br />Case Presentation: 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.<br />Conclusion: 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.

Details

Language :
English
ISSN :
1546-0096
Volume :
19
Issue :
1
Database :
MEDLINE
Journal :
Pediatric rheumatology online journal
Publication Type :
Academic Journal
Accession number :
34082764
Full Text :
https://doi.org/10.1186/s12969-021-00571-9