Abstract
We report a case of a patient with scleromyxedema limited to the skin with an associated IgG λ monoclonal protein treated successfully with high-dose dexamethasone. We encourage the continued investigation of this complex relationship between the clinical presentation of scleromyxedema and its frequently associated paraproteinemia.
Original language | English (US) |
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Pages (from-to) | 120-123 |
Number of pages | 4 |
Journal | Journal of the American Academy of Dermatology |
Volume | 51 |
Issue number | 2 |
DOIs | |
State | Published - Aug 2004 |
ASJC Scopus subject areas
- Dermatology