“…In pathology examination, PM is generally characterized with 1) infiltration of muscle with large eosinophilic giant cells and 2) proliferative fibroblasts mainly targeting the interfascicular connective tissue. In contrast to other similar disorders like myositis ossificans or nodular fasciitis, the actual muscle is not involved and largely preserved in PM [7] . After the establishment of the diagnosis, the recommended treatment strategy is no specific treatment, because PM might disappear spontaneously.…”