Literature DB >> 7738278

Systemic plasmacytosis: a case which improved with melphalan.

D W Lee1, S W Choi, J W Park, B K Cho.   

Abstract

Plasmacytosis, a distinctive proliferative disorder of plasma cells, is characterized by peculiar multiple skin eruptions, lymphadenopathy and polyclonal hypergammaglobulinemia. To date there has been no report of such cases showing remarkable responses to therapeutic agents. We herein report a case of plasmacytosis which developed in a 52-year-old Korean man and showed remarkable improvement with melphalan.

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Year:  1995        PMID: 7738278     DOI: 10.1111/j.1346-8138.1995.tb03372.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  2 in total

1.  Cutaneous and systemic plasmacytosis on the face: Effective treatment of a case using thalidomide.

Authors:  Sheng Fang; Kui Shan; Ai-Jun Chen
Journal:  Oncol Lett       Date:  2016-01-25       Impact factor: 2.967

2.  A Rare Case of Cutaneous Plasmacytosis in a Korean Male.

Authors:  Corey Georgesen; Meenal Kheterpal; Melissa Pulitzer
Journal:  Case Rep Pathol       Date:  2017-08-07
  2 in total

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