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Published on: August 18, 2022
Malignancy-associated Multicentric Reticulohistocytosis Mimicking Dermatomyositis-like Features, with a Significant
Hirotake Inomata1, Shinya Asatani1, Natsumi Ikumi2
1Division of Hematology and Rheumatology, School of Medicine, Nihon University, Japan.
Abstract:
Multicentric reticulohistocytosis (MRH) is a rare systemic non-Langerhans cell histiocytosis characterized by destructive polyarthritis and nodular skin lesions, often associated with malignancy. We present the case of a 74-year-old Japanese man initially suspected of having dermatomyositis due to polyarthritis, typical skin manifestations, and laboratory findings. Malignancy screening revealed invasive bladder cancer, which necessitated surgery and chemotherapy. Although the skin symptoms improved, aggressive joint destruction persisted, and histopathological analyses confirmed MRH. Remarkably, ultrasonography revealed significant inflammation and tendon involvement, highlighting its diagnostic utility. This case emphasizes the challenge of distinguishing MRH from autoimmune diseases and the critical role of ultrasound in capturing destructive joint damage.
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