Rare diagnosis of locally advanced triple‑negative breast cancer with paraneoplastic dermatomyositis: A case report and literature review

Paraneoplastic dermatomyositis (DM) is a rare autoimmune condition that primarily affects the skin and muscles; it is associated with various malignancies, including breast cancer. The present case report investigates the clinical presentation, therapeutic considerations and relevant literature regarding DM in the context of locally advanced triple-negative breast cancer (TNBC). A 43-year-old female patient presented with progressive myalgia, dysphagia and characteristic skin rashes. Subsequent investigations confirmed locally advanced TNBC and concomitant DM. Due to the severely weakened state of the patient, the standard treatment of neoadjuvant chemotherapy was contraindicated. The patient initially received corticosteroid therapy, which led to partial symptom improvement, followed by a modified radical mastectomy and adjuvant chemotherapy. Following surgical intervention, the patient experienced significant alleviation of DM symptoms. The present study underscores the critical role of early malignancy identification and intervention in managing DM associated with breast cancer; in addition, it explores the epidemiology, risk factors, pathogenesis, diagnostic modalities and treatment strategies for breast cancer-associated DM. The potential challenges in treatment selection are highlighted, particularly in patients with severe presentations. Mastectomy can emerge as a viable therapeutic option to achieve symptom control and facilitate subsequent oncological management.

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Publication Details

Journal
Oncology Letters
Published
2025-04-23
DOI
https://doi.org/10.3892/ol.2025.15055
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
0.00

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article

Rare diagnosis of locally advanced triple‑negative breast cancer with paraneoplastic dermatomyositis: A case report and literature review

Yu Song, Xin Huang, Ying Xu, Qiang Sun et al.
Oncology Letters
Inflammatory Myopathies and Dermatomyositis
article

Rare diagnosis of locally advanced triple‑negative breast cancer with paraneoplastic dermatomyositis: A case report and literature review

Yu Song, Xin Huang, Ying Xu, Qiang Sun, Yan Lin
article en

Abstract

Paraneoplastic dermatomyositis (DM) is a rare autoimmune condition that primarily affects the skin and muscles; it is associated with various malignancies, including breast cancer. The present case report investigates the clinical presentation, therapeutic considerations and relevant literature regarding DM in the context of locally advanced triple-negative breast cancer (TNBC). A 43-year-old female patient presented with progressive myalgia, dysphagia and characteristic skin rashes. Subsequent investigations confirmed locally advanced TNBC and concomitant DM. Due to the severely weakened state of the patient, the standard treatment of neoadjuvant chemotherapy was contraindicated. The patient initially received corticosteroid therapy, which led to partial symptom improvement, followed by a modified radical mastectomy and adjuvant chemotherapy. Following surgical intervention, the patient experienced significant alleviation of DM symptoms. The present study underscores the critical role of early malignancy identification and intervention in managing DM associated with breast cancer; in addition, it explores the epidemiology, risk factors, pathogenesis, diagnostic modalities and treatment strategies for breast cancer-associated DM. The potential challenges in treatment selection are highlighted, particularly in patients with severe presentations. Mastectomy can emerge as a viable therapeutic option to achieve symptom control and facilitate subsequent oncological management.

Oncology LettersVol. 29(6)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN)
Peking Union Medical College Hospital
Good health and well-being
Openalex Percentile: Top 88%
Inflammatory Myopathies and Dermatomyositis
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