Juvenile eosinophilic fasciitis: three case reports with review of the literature.

Abstract:

OBJECTIVES:Eosinophilic fasciitis is an uncommon scleroderma-like disorder characterised by induration and thickening of skin and soft tissue, usually associated with peripheral eosinophilia, poorly characterised in childhood. METHODS:We report 3 paediatric cases of eosinophilic fasciitis showing unusual clinical and histopathological features with a review of the literature. RESULTS:All cases presented progressive motility impairment started from upper limbs with no skin abnormalities. All cases showed systemic inflammatory involvement and 2 patients had acute complications. Two patients developed disabling outcomes despite appropriate treatments. CONCLUSIONS:Eosinophilic fasciitis may present unusual clinical and histopathological features during childhood and requires early recognition in order to prevent acute complications and disabling outcomes.

journal_name

Clin Exp Rheumatol

authors

Papa R,Nozza P,Granata C,Caorsi R,Gattorno M,Martini A,Picco P

subject

Has Abstract

pub_date

2016-05-01 00:00:00

pages

527-30

issue

3

eissn

0392-856X

issn

1593-098X

pii

9623

journal_volume

34

pub_type

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