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- W2320177414 startingPage "189" @default.
- W2320177414 abstract "Scleromyxedema (papular mucinosis) is a rare disorder characterized by proliferation of fibroblasts and cutaneous deposition of acid mucopolysaccharides, usually without disturbances of thyroid function. Associated abnormal proteins in the serum, identified as paraproteins, are a main feature of this disease. The association of scleromyxedema with classicial plasmacytoma or multiple myeloma is extremely rare. We report a case of scleromyxedema associated with multiple myeloma of the IgG lambda type." @default.
- W2320177414 created "2016-06-24" @default.
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- W2320177414 date "1983-06-01" @default.
- W2320177414 modified "2023-10-14" @default.
- W2320177414 title "Scleromyxedema associated with IgG lambda multiple myeloma" @default.
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- W2320177414 doi "https://doi.org/10.3949/ccjm.50.2.189" @default.
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