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Angiosarcoma of the breast: A review
Ran An1,2, Xiao-Juan Men2, Xi-Hao Ni1
1School of Clinical Medicine, Shandong Second Medical University, Weifang 261041, Shandong Province, China.
Heliyon
|February 6, 2024
Summary
Breast angiosarcoma is a rare, aggressive cancer. This review clarifies its causes, symptoms, and diverse pathology to aid clinicians in diagnosis and treatment, despite unclear guidelines.
Area of Science:
- Oncology
- Surgical Pathology
Background:
- Breast angiosarcoma is a rare, aggressive malignancy with poor prognosis.
- Etiology, pathogenesis, and diagnostic specificity remain unclear.
- Associated factors include radiation therapy and chronic lymphedema.
Purpose of the Study:
- To review the etiology, clinical manifestations, pathological features, imaging findings, treatment, and prognosis of breast angiosarcoma.
- To enhance clinicians' understanding and reduce misdiagnosis.
- To provide insights into current treatment strategies and challenges.
Main Methods:
- Comprehensive literature review.
- Analysis of clinical, pathological, and imaging data.
- Synthesis of information on etiology, diagnosis, and management.
Main Results:
- Breast angiosarcoma presents with non-specific symptoms and diverse pathological features, often leading to diagnostic challenges.
- Surgical excision with optimal margins is the primary treatment, though optimal approaches vary.
- Adjuvant radiotherapy and chemotherapy lack clear consensus and proven efficacy.
Conclusions:
- Accurate diagnosis requires a high index of suspicion and comprehensive evaluation.
- Multidisciplinary management tailored to individual patient factors is crucial.
- Further research is needed to establish clear diagnostic criteria and optimize treatment protocols.
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