Scleromyxedema: clinical diagnosis and autopsy findings
Abstract 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...
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Format: | Book |
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Sociedade Brasileira de Dermatologia,
2016-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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