Literature DB >> 6754236

Eosinophilic fasciitis.

L A Sibrack, E M Mazur, R Hoffman, A J Bollet.   

Abstract

Eosinophilic fasciitis (EF, a diffuse fasciitis with eosinophilia) is a recently recognized connective tissue disorder. It consists of deeply indurated, bound-down plaques of skin and subcutaneous tissue, most commonly present on the extremities. It is associated with peripheral eosinophilia, hypergammaglobulinaemia and an elevated sedimentation rate. There is usually no evidence of Raynaud's phenomenon, acral sclerosis or visceral involvement. Antinuclear antibodies are usually absent. The abnormal histopathology primarily involves the lower subcutis and the fascia. The clinical and laboratory features usually improve following the administration of systemic corticosteroids. Serious haematological abnormalities have been associated with eosinophilic fasciitis (EF) and have been discussed in detail. The similarities and distinctions between eosinophilic fasciitis and scleroderma have been discussed.

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Year:  1982        PMID: 6754236

Source DB:  PubMed          Journal:  Clin Rheum Dis        ISSN: 0307-742X


  4 in total

Review 1.  Mixed connective tissue disease, overlap syndromes, and eosinophilic fasciitis.

Authors:  P J Maddison
Journal:  Ann Rheum Dis       Date:  1991-11       Impact factor: 19.103

2.  An unusual soft tissue tumour and peripheral eosinophilia.

Authors:  B Banerjee; M Nashi; G R Dixon
Journal:  Postgrad Med J       Date:  1998-07       Impact factor: 2.401

3.  Eosinophilic fasciitis in association with chronic vasculitic-like leg ulcerations.

Authors:  A L Wong; N Anderson-Wilms; S E Mortensen; K K Colburn
Journal:  Clin Rheumatol       Date:  1993-03       Impact factor: 2.980

4.  Eosinophilic fasciitis presenting as psoriatic arthropathy.

Authors:  G D Wright; C Thornton; D A Keegan; A L Bell
Journal:  Ulster Med J       Date:  1992-04
  4 in total

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