HIGHLIGHTS
- who: Shang-shang Wang et al. from the Institute of Biochemistry and Biophysics (PAN), Poland Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China have published the Article: Case report: Scleromyxedema associated with a monoclonal gammapathy: Successful treatment with intravenous immunoglobulins, in the Journal: (JOURNAL)
SUMMARY
Scleromyxedema is a rare, chronic form of cutaneous mucinosis characterized by numerous, closely spaced waxy papules and diffuse skin induration that usually affects middle-aged adults aged between 30 and 80 years. Diagnosis is based on clinical findings of a generalized papular and sclerodermoid eruption; a typical . . .
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