| Literature DB >> 28477693 |
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.Entities:
Keywords: Autoimmunity; Dermatomyositis/polymyositis; Juvenile; Lymphoma
Mesh:
Year: 2017 PMID: 28477693 DOI: 10.1016/j.jns.2017.03.033
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181