eosinophilic fasciitis


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e·o·sin·o·phil·ic fas·ci·i·tis

[MIM*226350]
induration and edema of the connective tissues of the extremities, usually appearing following exertion; associated with elevated sedimentation rate, elevated IgG, and eosinophilia.
Synonym(s): Shulman syndrome

eosinophilic fasciitis

inflammation of fasciae of the limbs, associated with eosinophilia, edema, and swelling. The cause is unknown, but the condition often occurs after strenuous exercise. Also called Shulman's syndrome.
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Eosinophilic fasciitis

eosinophilic fasciitis

Inflammation of muscle fascia, associated with eosinophilia, pain, and swelling.
See also: fasciitis

Shulman,

Lawrence Edward, U.S. rheumatologist, 1919–.
Shulman syndrome - induration and edema of the connective tissues of the extremities, usually appearing following exertion. Synonym(s): eosinophilic fasciitis
References in periodicals archive ?
The features were compatible with eosinophilic fasciitis.
Eosinophilic fasciitis is a scleroderma-like syndrome of unknown cause characterized by inflammation, followed by sclerosis of the dermis, subcutis, and deep fascia.
The presentation of this patient with itchy reddish and swollen skin lesion was not typical of eosinophilic fasciitis at the beginning, leading to a reasonable delay in diagnosis, especially as it is a rare disease.
Eosinophilic fasciitis (also called Shul-man's syndrome) is a rare, localized, fibrosing disorder of subcutaneous tissues.
Eosinophilic fasciitis is slightly more common in middle-aged men, but can occur in women and children.
In eosinophilic fasciitis, low- to moderate-dose prednisone (20-30 mg)--and, if needed, methotrexate as a steroid-sparing agent--can be given, Dr.
Eosinophilic fasciitis (EF) is a rare condition, characterized by generalized induration of the skin and subcutaneous tissues.
Eosinophilia-myalgia syndrome, eosinophilic fasciitis, and related fibrosing disorders.
Eosinophilic fasciitis (EF) is a rare inflammatory disease of unknown etiology.
Eosinophilic fasciitis (EF) is a rare disease, first identified in 1974 by Shulman (1).
When the woman was admitted, the differential diagnosis was between scleroderma and eosinophilic fasciitis (also known as generalized morphea profunda), according to Dr.
Histology showed deep dermal fibrosis with fibrosis of fat septa extending down to a thickened fascial layer, which is confirmatory for eosinophilic fasciitis, said Dr.

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