Paraneoplastic myopathy in pancreatic cancer: a case report and literature review

Dermatomyositis (DM) and polymyositis (PM) are both immune-mediated inflammatory myopathies known to occur in paraneoplastic syndromes associated with a new diagnosis of malignancy, most commonly breast, ovarian, lung, pancreatic, stomach, colorectal, and Non-Hodgkin’s lymphoma1 in DM and breast, lu...

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Veröffentlicht in:Journal of community hospital internal medicine perspectives 2021-11, Vol.11 (6), p.847-851
Hauptverfasser: Padniewski, Jessica Joanne, Nelson, Elizabeth, Mian, Istiaq, Laczniak, Andrew, Ives, Samuel, Nasr, Rawad
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Sprache:eng
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Zusammenfassung:Dermatomyositis (DM) and polymyositis (PM) are both immune-mediated inflammatory myopathies known to occur in paraneoplastic syndromes associated with a new diagnosis of malignancy, most commonly breast, ovarian, lung, pancreatic, stomach, colorectal, and Non-Hodgkin’s lymphoma1 in DM and breast, lung, bladder cancer, and Non-Hodgkin’s lymphoma in PM. 2,3,4 While inflammatory markers such as creatine kinase (CK) may be elevated with either DM or PM, marked elevation is rare. Herein, we report a case of newly diagnosed pancreatic cancer presenting with inflammatory myopathy and marked CK elevation. We review the frequency of PM as a paraneoplastic syndrome, the association with marked CK elevation, and the association with pancreatic cancer.
ISSN:2000-9666
2000-9666
DOI:10.1080/20009666.2021.1982487