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Title: Juvenile dermatomyositis/polymyositis and lymphoma. Author: Stübgen JP. Journal: J Neurol Sci; 2017 Jun 15; 377():19-24. PubMed ID: 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.[Abstract] [Full Text] [Related] [New Search]