Amyopathic Dermatomyositis Revealing Triple-Negative Breast Cancer: A Case Report and Literature Review

Amyopathic dermatomyositis (ADM) is a rare form of dermatomyositis characterized by specific cutaneous lesions without muscle involvement. It can reveal an underlying malignancy, particularly breast carcinoma. We report the case of a 48-year-old woman presenting with a skin eruption suggestive of ADM, preceding the diagnosis of triple-negative breast cancer. Paraneoplastic etiology was confirmed by the presence of anti-TIF1γ antibodies. Management included corticosteroids, intravenous immunoglobulins, and neoadjuvant chemotherapy followed by mastectomy, resulting in rapid improvement in cutaneous manifestations. One-year post-treatment, no recurrence has been observed. This case highlights the importance of systematic oncologic screening in ADM and the value of multidisciplinary care.

Authors

Publication Details

Journal
Scholars Journal of Medical Case Reports
Published
2025-09-09
DOI
https://doi.org/10.36347/sjmcr.2025.v13i09.014
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Amyopathic Dermatomyositis Revealing Triple-Negative Breast Cancer: A Case Report and Literature Review

Adil Chaouni, Hafid Hachi, Nezha Elbahaoui, Hajar Kandoussi et al.
Scholars Journal of Medical Case Reports
Inflammatory Myopathies and Dermatomyositis
article

Amyopathic Dermatomyositis Revealing Triple-Negative Breast Cancer: A Case Report and Literature Review

Adil Chaouni, Hafid Hachi, Nezha Elbahaoui, Hajar Kandoussi, Marouane Oucharqui
article en

Abstract

Amyopathic dermatomyositis (ADM) is a rare form of dermatomyositis characterized by specific cutaneous lesions without muscle involvement. It can reveal an underlying malignancy, particularly breast carcinoma. We report the case of a 48-year-old woman presenting with a skin eruption suggestive of ADM, preceding the diagnosis of triple-negative breast cancer. Paraneoplastic etiology was confirmed by the presence of anti-TIF1γ antibodies. Management included corticosteroids, intravenous immunoglobulins, and neoadjuvant chemotherapy followed by mastectomy, resulting in rapid improvement in cutaneous manifestations. One-year post-treatment, no recurrence has been observed. This case highlights the importance of systematic oncologic screening in ADM and the value of multidisciplinary care.

Scholars Journal of Medical Case ReportsVol. 13(09)
Openalex Percentile: Top 67%
Inflammatory Myopathies and Dermatomyositis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.