Cutaneous and systemic plasmacytosis showing histopathologic features as mixed-type Castleman disease: a case report.

@article{Chen2012CutaneousAS,
  title={Cutaneous and systemic plasmacytosis showing histopathologic features as mixed-type Castleman disease: a case report.},
  author={Hao Chen and Yanning Xue and Yiqun Jiang and Xuesi Zeng and Jian-Fang Sun},
  journal={The American Journal of dermatopathology},
  year={2012},
  volume={34 5},
  pages={
          553-6
        }
}
  • Hao Chen, Yanning Xue, +2 authors Jian-Fang Sun
  • Published in
    The American Journal of…
    2012
  • Medicine
  • Cutaneous and systemic plasmacytosis (CSP) is a rare disorder characterized by disseminated reddish brown plaques and polyclonal hypergammaglobulinemia. The lesions of CSP are histologically characterized by an infiltration of mature polyclonal plasma cells, which display similar pathological features to the plasma cell-type Castleman disease (CD). The relationship between CSP and CD is controversial. Herein, we described a 43-year-old man from China with disseminated reddish brown plaques and… CONTINUE READING

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