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Scleromyxedema without paraproteinemia

✍ Scribed by Abarzúa, Alvaro A.; Giesen, Laura F.; Sandoval, Mauricio O.; González, Sergio B.

Book ID: 124163587
Publisher: John Wiley and Sons
Year: 2014
Tongue: English
Weight: 293 KB
Volume: 53
Category: Article
ISSN: 0011-9059
DOI: 10.1111/ijd.12124

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## Abstract Scleromyxedema is a rare disease characterized by papular mucinous deposits, dermal fibroblast proliferation, and a monoclonal paraproteinemia. Its chronic course tends to be complicated by gastrointestinal, muscular, pulmonary, and neurologic disorders. We review the literature to iden