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青少年皮肌炎/多发性肌炎与淋巴瘤

Juvenile dermatomyositis/polymyositis and lymphoma.

作者信息

Stübgen Joerg-Patrick

机构信息

Department of Neurology, Weill Cornell Medicine/New York Presbyterian Hospital, 525 East 68th Street, New York, NY 10065-4885, USA.

出版信息

J Neurol Sci. 2017 Jun 15;377:19-24. doi: 10.1016/j.jns.2017.03.033. Epub 2017 Mar 27.

Abstract

In patients with juvenile dermatomyositis/polymyositis (JDM/PM), malignancy is a rare phenomenon. An extensive workup for neoplastic disease is not routinely indicated, but should be considered if unusual physical findings are noted at JDM/PM diagnosis or during follow-up period. The objective of this literature review was to assess for any association between, and disease profile of, JDM/PM and lymphoma in childhood. Risk determinants of the possible development of lymphoma in the pediatric population with JDM/PM appear to be the degree and duration of inflammatory activity with chronic B-cell activation and/or antigen stimulation; a paraneoplastic relationship is unlikely.

摘要

在青少年皮肌炎/多发性肌炎(JDM/PM)患者中,恶性肿瘤是一种罕见现象。通常并不常规进行针对肿瘤性疾病的全面检查,但如果在JDM/PM诊断时或随访期间发现异常体征,则应予以考虑。本文献综述的目的是评估儿童JDM/PM与淋巴瘤之间的任何关联及其疾病特征。患有JDM/PM的儿科人群中可能发生淋巴瘤的风险决定因素似乎是伴有慢性B细胞活化和/或抗原刺激的炎症活动的程度和持续时间;不太可能存在副肿瘤关系。

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