Paraneoplastic Amyopathic Dermatomyositis Associated With a Bone and Medullary Location of Breast Adenocarcinoma
Fadwa Haboub, Mohamed El Fadli, Othmane Zouiten, Leila Afani, Rhizlane Belbaraka

TL;DR
A rare case of paraneoplastic amyopathic dermatomyositis linked to breast cancer highlights the need for early cancer detection and multidisciplinary care.
Contribution
This case report adds to the understanding of paraneoplastic ADM as an early sign of breast cancer with bone metastases.
Findings
Paraneoplastic ADM presented alongside bone metastases from breast adenocarcinoma in a 58-year-old woman.
Endocrine therapy and immunomodulators led to partial improvement, but the patient died from severe complications.
The case emphasizes the importance of recognizing ADM as a potential early indicator of malignancy.
Abstract
Paraneoplastic amyopathic dermatomyositis (ADM) is a rare connective tissue disease presenting with characteristic dermatomyositis-like skin findings in the absence of muscle involvement. It is associated with malignancies in 15%-30% of cases and may portend a fatal outcome, especially when linked to advanced cancers. We report the case of a 58-year-old woman who presented with progressive low back pain and erythroderma. Imaging revealed diffuse bone metastases, and bone biopsy confirmed a poorly differentiated adenocarcinoma of breast origin (estrogen receptor, 60%; progesterone receptor, 35%; GATA3 positive). Simultaneously, dermatological evaluation identified periungual erythema and other cutaneous findings consistent with ADM. The patient was started on endocrine therapy with palbociclib and letrozole, along with corticosteroids and hydroxychloroquine, resulting in partial…
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Taxonomy
TopicsInflammatory Myopathies and Dermatomyositis · Neurogenetic and Muscular Disorders Research · Heterotopic Ossification and Related Conditions
