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Scleromyxedema: clinical diagnosis and autopsy findings
Scleromyxedema is a rare chronic cutaneous mucinosis of unknown etiology. It is characterized by papular eruption and scleroderma with microscopic evidence of mucin deposition, fibroblast proliferation, and fibrosis. Most patients with scleromyxedema have monoclonal gammopathy and systemic manifesta...
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| Publicado en: | An Bras Dermatol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Sociedade Brasileira de Dermatologia
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5324991/ https://ncbi.nlm.nih.gov/pubmed/28300892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20164527 |
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