Dermatomyositis (DM) and polymyositis (PM) are both inflammatory conditions characterized by proximal muscle weakness and inflammation. Both conditions, particularly DM, have also been closely associated with an increased risk of malignancy. In one retrospective cohort study performed in Australia, 537 patients with biopsy-proven inflammatory myopathies were identified, and retrospectively assessed for concomitant malignancies. In these patients, 116 cases of malignancy were identified. Of the types of myositis, patients with dermatomyositis had the highest incidence of malignancy, with 42% of patients diagnosed with malignant disease, leading to a standardized incidence ratio of 6.2 (95% CI 3.9 to 10.0]. Polymyositis was also associated with malignant disease, though to a lesser degree with a standardized incidence ratio of only 2.0 (CI 1.4 to 2.7). The most common types of malignancy diagnosed are adenocarcinomas, including lung, gastric, ovarian, and pancreatic, though prevalence varies based on the underlying population and risk factors. Currently, the recommendation for patients diagnosed with DM or PM is to perform a basic laboratory evaluation and age-appropriate screening, with additional diagnostic imaging based on risk for malignancy and underlying symptoms.
References: Dermatomyositis and Malignancy