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皮肤浆细胞增多症：特发性多中心Castleman病的一种罕见初始表现。

Cutaneous plasmacytosis: A rare initial presentation of idiopathic multicentric Castleman's disease.

作者信息

Yamamoto Yu, Matsumura Masami

机构信息

Division of General Medicine, Center for Community Medicine Jichi Medical University Shimotsuke Japan.

出版信息

Clin Case Rep. 2021 May 4;9(5):e04109. doi: 10.1002/ccr3.4109. eCollection 2021 May.

DOI:10.1002/ccr3.4109
PMID:34026151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8122127/
Abstract

Cutaneous plasmacytosis could precede the development of idiopathic multicentric Castleman's disease (iMCD). If a patient is diagnosed with cutaneous plasmacytosis without systemic manifestations, clinicians should carefully follow up with the patient keeping in mind the potential for the development of iMCD.

摘要

皮肤浆细胞增多症可能先于特发性多中心Castleman病（iMCD）出现。如果患者被诊断为无全身表现的皮肤浆细胞增多症，临床医生应牢记iMCD发生的可能性，对患者进行密切随访。

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本文引用的文献

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Idiopathic multicentric Castleman disease preceded by cutaneous plasmacytosis successfully treated by tocilizumab.特发性多中心 Castleman 病继发皮肤浆细胞瘤，经托珠单抗治疗后获得良好疗效。
BMJ Case Rep. 2020 Nov 4;13(11):e236283. doi: 10.1136/bcr-2020-236283.
2
Cutaneous and systemic plasmocytosis.皮肤和全身浆细胞增多症。
J Dtsch Dermatol Ges. 2013 Dec;11(12):1161-7. doi: 10.1111/ddg.12190. Epub 2013 Aug 12.