Literature DB >> 610515

[Shulman's syndrome: fasciitis with eosinophilia, pseudoscleroderma with eosinophilia].

J Chevrant-Breton, M Mondaud, O Sabouraud, A Huguenin.   

Abstract

The authors report two cases of the Shulman's syndrome. Twenty one cases of this new entity are found in the literature. The main signs are the acute painful onset after an unusual physical exertion, the development of fasciitis, and (or) myositis, and (or) scleroderma of limbs, the absence of Raynaud's phenomenon, visceral involvement, constant eosinophilia and hypergammaglobulinemia; the prognosis is good with an improvement sometimes spontaneous or coincident with prednisone therapy. One of the observations is interesting by the association with Gougerot-Sjogren's syndrome, and a familial case of morphea. The prognosis in this case is mediocre: failure of corticotherapy, and incomplete remission with cyclophosphamide.

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Year:  1977        PMID: 610515

Source DB:  PubMed          Journal:  Ann Dermatol Venereol        ISSN: 0151-9638            Impact factor:   0.777


  4 in total

1.  Diffuse fasciitis.

Authors:  M M Steven; A Cats
Journal:  Clin Rheumatol       Date:  1984-09       Impact factor: 2.980

2.  [Eosinophilic fasciitis (Shulman syndrome)].

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

3.  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

4.  Diffuse (eosinophilic) fasciitis. A series of six cases.

Authors:  J M De Jonge-Bok; M M Steven; F Eulderink; A Cats
Journal:  Clin Rheumatol       Date:  1984-09       Impact factor: 2.980

  4 in total

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