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fasciitis/edema

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Atypical Presentation of Eosinophilic Fasciitis with Pitting Edema.

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Eosinophilic fasciitis (EF) is a rare condition involving inflammation of the fascia and peripheral eosinophilia of unknown etiology leading to tissue fibrosis. Clinical presentation includes peripheral eosinophilia, symmetrical skin thickening with subcutaneous tissue induration of the extremities

Finger stiffness or edema as presenting symptoms of eosinophilic fasciitis.

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To investigate the clinical features and finger symptoms of eosinophilic fasciitis (EF), we reviewed five patients with EF. The chief complaint was pain, edema and/or stiffness of the extremities. The distal extremities were affected in all patients, and there was also proximal involvement in one

MR imaging of plantar fasciitis: edema, tears, and occult marrow abnormalities correlated with outcome.

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OBJECTIVE We sought to evaluate various MR imaging signs of plantar fasciitis and to determine if a difference in these findings exists between clinically typical and atypical patients with chronic symptoms resistant to conservative treatment. CONCLUSIONS We found signs on MR imaging that, to our

A case of eosinophilic fasciitis presenting as pitting edema of the lower extremities.

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Eosinophilic fasciitis is a rare disease characterized by diffuse fasciitis with peripheral eosinophilia and progressive induration and thickening of the skin and soft tissues. We report a 19-year-old female who presented with pitting edema in both lower extremities. She had a history of excessive

Plantar Fasciitis and Bone Marrow Edema in Brucellosis.

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Eosinophilic fasciitis: an uncommon cause of edema.

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Eosinophilic fasciitis presenting as pitting edema of the extremities.

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Pyoderma gangrenosum (PG) is associated with systemic disease, mostly rheumatoid arthritis (RA) and inflammatory bowel disease (IBD), in many patients (more than 50%). Lesions associated with arthritis are often ulcerative. Although these lesions typically affect the lower limbs, they can also

A case of eosinophilic fasciitis without skin manifestations: a case report in a patient with lupus and literature review

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Eosinophilic fasciitis (EF) is a rare connective tissue disease that causes inflammation and fibrosis of the fascia, inducing pain and motor dysfunction. Characteristic skin manifestations, such as edema, erythema, induration, peau d'orange appearance, and the groove sign, are of diagnostic

Antisynthethase syndrome presenting as peripheral limb fasciitis.

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Inflammatory myopathy is a major clinical manifestation of the antisynthetase syndrome. Patients with anti Jo-1 antibodies can also present with other clinical manifestations as arthritis, mechanic's hands and lung fibrosis. As in dermatomyositis, polymyositis and overlap myopathies proximal muscle

[Eosinophilic fasciitis--a case report].

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Eosinophilic fasciitis characterized by symmetrical limbs' edema, myalgia, erythema, and progressive cutaneous and subcutaneous induration. Peripheral eosinophilia and hypergammaglobulinaemia are the most characteristic features of the disease. Histopathological examination shows fibrosis of fascia

Diffuse abdominal wall cellulitis in ascending omphalitis--a lethal association in neonatal necrotizing fasciitis.

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Necrotizing fasciitis is a grave complication of ascending omphalitis in the neonate, but because it is rare some of the signs are not well documented. Rapidly progressive anterior abdominal wall edema and cellulitis were noted in 16 patients who were clinically diagnosed with necrotizing fasciitis.

Eosinophilic fasciitis: an atypical presentation of a rare disease.

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Eosinophilic fasciitis, or Shulman's disease, is a rare disease of unknown etiology. It is characterized by peripheral eosinophilia, hypergammaglobulinemia, and high erythrocyte sedimentation rate. The diagnosis is confirmed by a deep biopsy of the skin. The first line of treatment is

[Shulman's syndrome (eosinophilic fasciitis)].

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Eosinophilic fasciitis is a rare disease characterized by edema, painful indurations, and progressive muscle weakness. Mainly the extremities are involved. We report on a 22-year-old woman with eosinophilic fasciitis presenting with progressive muscle weakness of both hands and feet and a reduced

A case of eosinophilic fasciitis and generalized morphea overlap.

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A 60-year old man developed skin hardening and edema on his extremities. Although he had been treated with oral prednisolone at another hospital, skin stiffness relapsed during tapering of prednisolone. At the initial visit to our department, physical examination showed skin hardening of the
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