| Literature DB >> 26998101 |
Sheng Fang1, Kui Shan1, Ai-Jun Chen1.
Abstract
Cutaneous and systemic plasmacytosis is an exceedingly rare condition that is identified in Japanese individuals in particular. The present study describes the case of a patient of mainland Chinese origin who manifested with red-brown macules, papules and plaques limited to the face. Identifying a therapy for cutaneous and systemic plasmacytosis is quite difficult, however, the present patient showed a good response to low-dose thalidomide. The exact mechanism of action is not yet clear, however, we hypothesize that thalidomide may function through decreasing the secretion of interleukin-6 and affecting the growth of plasma cells.Entities:
Keywords: hypergammaglobulinemia; lymphadenopathy; plasmacytosis
Year: 2016 PMID: 26998101 PMCID: PMC4774603 DOI: 10.3892/ol.2016.4140
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967