Results 111 to 120 of about 562 (139)
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Archives of Dermatology, 1966
Two patients with typical skin lesions of scleromyxedema (lichen myxedematosus) are described. The disorder is characterized by proliferation of fibroblasts and excessive deposition of acid mucopolysaccharides in the dermis. Quantitative elevated levels of acid mucopolysaccharides were demonstrated in the serum and skin of one patient.
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Two patients with typical skin lesions of scleromyxedema (lichen myxedematosus) are described. The disorder is characterized by proliferation of fibroblasts and excessive deposition of acid mucopolysaccharides in the dermis. Quantitative elevated levels of acid mucopolysaccharides were demonstrated in the serum and skin of one patient.
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New England Journal of Medicine, 2023
Soumya Chatterjee, Anthony P. Fernandez
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Soumya Chatterjee, Anthony P. Fernandez
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Dermatologie (Heidelberg, Germany)
Scleromyxedema or generalized diffuse lichen myxoedematosus is a rare mucinosis that is associated with monoclonal gammopathy and which frequently affects multiple extracutaneous organ systems. The pathogenesis of scleromyxedema has not been fully elucidated, but includes stimulation of glycosaminoglycan synthesis. The clinical course of scleromyxedema
Cord, Sunderkötter +2 more
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Scleromyxedema or generalized diffuse lichen myxoedematosus is a rare mucinosis that is associated with monoclonal gammopathy and which frequently affects multiple extracutaneous organ systems. The pathogenesis of scleromyxedema has not been fully elucidated, but includes stimulation of glycosaminoglycan synthesis. The clinical course of scleromyxedema
Cord, Sunderkötter +2 more
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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 ...
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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
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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
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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
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Histopathologic characteristics of scleromyxedema: A study of a series of 34 cases
Journal of the American Academy of Dermatology, 2016, Franco Rongioletti, Bernard Cribier
exaly