PT  - JOURNAL ARTICLE
AU  - Marsha L. Muldrow
AU  - Philip L. Bailin
TI  - Scleromyxedema associated with IgG lambda multiple myeloma
DP  - 1983 Jun 20
TA  - Cleveland Clinic Journal of Medicine
PG  - 189--195
VI  - 50
IP  - 2
4099  - http://www.ccjm.org/content/50/2/189.short
4100  - http://www.ccjm.org/content/50/2/189.full
SO  - Cleve Clin J Med1983 Jun 20; 50
AB  - 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.