Results 141 to 150 of about 773 (166)
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Cutis, 1980
Scleromyxedema (also known as lichen myxedematosus or papular mucinosis) is a rare cutaneous disorder characterized by lichenoid waxy papules, sclerosis, and a characteristic paraproteinemia. Rarely, if ever, is there systemic involvement. The cause and pathogenesis remain a mystery, however, a recent report has linked a serum factor with fibroblast ...
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Scleromyxedema (also known as lichen myxedematosus or papular mucinosis) is a rare cutaneous disorder characterized by lichenoid waxy papules, sclerosis, and a characteristic paraproteinemia. Rarely, if ever, is there systemic involvement. The cause and pathogenesis remain a mystery, however, a recent report has linked a serum factor with fibroblast ...
openaire +1 more source
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2019
Scleromyxedema is a rare disorder that frequently affects multiple extracutaneous organ systems and is usually associated with monoclonal gammopathy. The pathogenesis of scleromyxedema is unknown. The clinical course is chronic and progressive and can lead to marked morbidity or death.
M, Neufeld +2 more
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Scleromyxedema is a rare disorder that frequently affects multiple extracutaneous organ systems and is usually associated with monoclonal gammopathy. The pathogenesis of scleromyxedema is unknown. The clinical course is chronic and progressive and can lead to marked morbidity or death.
M, Neufeld +2 more
openaire +1 more source
Zeitschrift fur Hautkrankheiten, 1986
In a 51-year-old man scleromyxedema developed gradually from mucinosis papulosa over 13 years. Paraproteins of the type IgG-lambda were discovered in this patient.
E, Varga, A, Kiss, I, Schneider
openaire +1 more source
In a 51-year-old man scleromyxedema developed gradually from mucinosis papulosa over 13 years. Paraproteins of the type IgG-lambda were discovered in this patient.
E, Varga, A, Kiss, I, Schneider
openaire +1 more source
Scleromyxedema in an adult following Sinopharm BBIBP-CorV vaccination: An extremely rare phenomenon
Journal of Scleroderma and Related Disorders, 2023Amirhossein Parsaei +2 more
exaly
Acute rhabdomyolysis during the treatment of scleromyxedema with interferon alfa
Journal of Dermatological Treatment, 2001A Akar
exaly

