Scleredema of Buschke Successfully Treated With Electron Beam Therapy

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منابع مشابه

Scleredema of Buschke successfully treated with electron beam therapy.

A 58-year-old white woman with an 11-year history of type 1 diabetes mellitus presented in April 1995 with a complaint of flushing of the neck and the upper part of her trunk. She had had no antecedent febrile illness. The flushing resolved within a few days, but approximately 1 month later, the patient developed thickening and induration of the skin of the posterior section of her neck (Figure...

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Scleredema adultorum of Buschke treated with radiation.

BACKGROUND Scleredema adultorum of Buschke is an uncommon skin condition that may accompany diabetes mellitus. Current therapeutic options are poor, with only case reports and small series supporting their use. OBSERVATION We describe 3 patients with severe restrictive scleredema associated with type 2 diabetes mellitus who responded to radiation therapy after other treatments had failed. Ang...

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Electron beam therapy in patients with scleredema.

treatment with diphencyprone. Z Hautkr 1984; 59: 1080 ± 1083. 3. Weisshaar E, Neumann H-J, Gollnick H. Successful treatment of disseminated facial verrucae with contact immunotherapy. Eur J Dermatol 1998; 8: 488 ± 491. 4. Greenberg JH, Smith TL, Katz RM. Verrucae vulgares rejection. A preliminary study on contact dermatitis and cellular immune response. Arch Dermatol 1973; 107: 580 ± 582. 5. La...

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Long-term benefit of electron beam radiation therapy in the treatment of scleredema of Buschke

INTRODUCTION Scleredema of Buschke is a rare connective tissue disorder presenting with woody thickening and induration of the nuchal and shoulder regions resulting in progressive decrease in the range of motion of the neck. Treatment options include several forms of systemic therapy with variable results. Local radiation therapy (RT) is often thought of as a secondary form of therapy. Few repo...

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Scleredema of Buschke.

Main text A 46-year-old African-American male with a history of type-1 diabetes (DM) was referred to the Rheumatology clinic for a further evaluation of possible systemic scleroderma. He reported a 3-year history of skin thickening and hyperpigmentation on his back and shoulders. Over the last 12 months, his symptoms progressed, involving the proximal arms, legs, and back with sparing of his ha...

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ژورنال

عنوان ژورنال: Archives of Dermatology

سال: 1998

ISSN: 0003-987X

DOI: 10.1001/archderm.134.4.419