84. Eosinophilic fasciitis

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Eosinophilic fasciitis*

Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocyte sedimentation rate can be seen. Clinical features begin acutely, with local edema and a painfu...

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Eosinophilic fasciitis in siblings.

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Eosinophilic fasciitis: MRI evaluation.

We conducted repeat muscle MR imaging (figure) on a 46-yearold man with relapsing eosinophilic fasciitis that can be classified in a continuum around the so-called Shulman syndrome.1 The patient had a 6-month history of relapsing fever and pain and swelling of the lower limbs, which responded to a moderate dosage of corticosteroids but relapsed several times after tapering of corticosteroids. I...

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Eosinophilic fasciitis after parasite infection

Eosinophilic fasciitis is a systemic inflammatory disease characterized by symmetrical swelling and skin induration of the distal portions of the arms and/or legs, evolving into a scleroderma-like appearance, accompanied by peripheral blood eosinophilia. It is a rare disease with a poorly understood etiology. Corticosteroid treatment remains the standard therapy, either taken alone or in associ...

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Two cases of eosinophilic fasciitis.

Eosinophic fasciitis (EF) is an uncommon connective tissue disease characterized by scleroderma-like cutaneous changes, peripheral eosinophilia, hypergammaglobulinemia, and an elevated erythrocyte sedimentation rate (ESR). Typical histopathologic findings include chronic inflammatory infiltration affecting the deep fascia with lymphocytes, histiocytes, and occasionally eosinophils. We report tw...

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ژورنال

عنوان ژورنال: Rheumatology Advances in Practice

سال: 2018

ISSN: 2514-1775

DOI: 10.1093/rap/rky034.047