Cutaneous and systemic plasmacytosis

Cutaneous and systemic plasmacytosis （CSP） is a rare condition characterized by a clinical triad of cutaneous lesions, polyclonal hypergammaglobulinemia, and superficial lymphadenopathy. The condition is described primarily in middle-aged Asian patients and particular in Japanese individuals,l A pre...

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Bibliographic Details
Published inChinese medical journal Vol. 125; no. 22; pp. 4156 - 4157
Main Authors Cheng, Ru-hong, Yu, Hong, Li, Ming, Yao, Zhi-rong
Format Journal Article
LanguageEnglish
Published China Department of Dermatology,Xinhua Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai 200092,China 20.11.2012
Subjects
Adult
CSP
Humans
Male
Plasma Cells - pathology
Skin Diseases - diagnosis
丙种球蛋白
中位数
多克隆
年龄
患者
淋巴结肿大
皮肤损伤
Chinese
cutaneous and systemic plasmacytosis
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Summary:Cutaneous and systemic plasmacytosis （CSP） is a rare condition characterized by a clinical triad of cutaneous lesions, polyclonal hypergammaglobulinemia, and superficial lymphadenopathy. The condition is described primarily in middle-aged Asian patients and particular in Japanese individuals,l A previous study suggest a male ： female ratio of 1 to 0.6, and an age of onset ranging from 20 to 62 years, with both a mean and median age of 37 years.2 Here, we report a Chinese case of CSP, who is the youngest patient of Chinese decent in literature.
Bibliography:Cutaneous and systemic plasmacytosis （CSP） is a rare condition characterized by a clinical triad of cutaneous lesions, polyclonal hypergammaglobulinemia, and superficial lymphadenopathy. The condition is described primarily in middle-aged Asian patients and particular in Japanese individuals,l A previous study suggest a male ： female ratio of 1 to 0.6, and an age of onset ranging from 20 to 62 years, with both a mean and median age of 37 years.2 Here, we report a Chinese case of CSP, who is the youngest patient of Chinese decent in literature.
cutaneous and systemic plasmacytosis; Chinese
11-2154/R
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0366-6999
2542-5641
DOI:10.3760/cma.j.issn.0366-6999.2012.22.048