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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.

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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