| Literature DB >> 18572979 |
Selmin Ataergin1, Fikret Arpaci, Murat Demiriz, Ahmet Ozet.
Abstract
Scleromyxedema is a rare disorder characterized by mucin deposits in the dermis and monoclonal gammopathy. No definitive treatment of this condition has been described to date. We present the case of a 38-year-old male patient with scleromyxedema who underwent double consecutive autologous peripheral stem cell transplantations and received immunoglobulin, thalidomide, and bortezomib. This resulted in considerable clinical and pathologic amelioration of the patient's condition. However, 3 years after the second transplant, the patient relapsed and manifested the same skin lesions evident at his initial presentation.Entities:
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Year: 2008 PMID: 18572979 DOI: 10.2165/00128071-200809040-00008
Source DB: PubMed Journal: Am J Clin Dermatol ISSN: 1175-0561 Impact factor: 7.403