Literature DB >> 7456771

[Eosinophilic fasciitis. A recently reported oligotopic connective tissue inflammation. A case report].

M Giordano, M Ara, R Rossiello, C Cicala, G Valentini.   

Abstract

A 25 year old suffering from eosinophilic fasciitis is reported. This patient showed periostitis at some bones and myatrophy of thenar and hypothenar besides the typical manifestations related to the involvement of fascia and nearby tissues. On the whole these manifestations reduced the patient's mobility seriously. The typical humoral findings of eosinophilic fasciitis were present, i. e. remarkable eosinophilia, hypergammaglobulinemia with rise of Ig G, and inflammatory serum alterations. Furthermore an increase urinary hydroxyproline excretion was found which means an altered collagen metabolism. This is obviously related to collagen accumulation that in this patient was observed at fascia, perimysium and in the subcutaneous tissue. Ig G deposits were found in the fascia. The reported case raised some problems of differential diagnosis with polymyositis, progressive systemic sclerosis, localized scleroderma and, perhaps, mixed connective tissue disease.

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Year:  1980        PMID: 7456771

Source DB:  PubMed          Journal:  Z Rheumatol        ISSN: 0340-1855            Impact factor:   1.372


  2 in total

1.  [Eosinophilic fasciitis (Shulman syndrome)].

Authors:  P Herzer; H S Füessl; M Meurer; M Schattenkirchner
Journal:  Klin Wochenschr       Date:  1982-11-02

2.  Presence of eosinophilia in progressive systemic sclerosis and localized scleroderma.

Authors:  M Giordano; M Ara; G Valentini; U Chianese; T Bencivenga
Journal:  Arch Dermatol Res       Date:  1981       Impact factor: 3.017

  2 in total

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