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Angiosarcoma of breast and chest wall complicated with tuberculous empyema: A case report

Angiosarcoma is a highly malignant endothelial tumor, accounting for 1% to 2% of soft tissue sarcomas. The most common site of the disease is the skin, accounting for approximately 60% of cases, especially the skin of the head. It can also occur in soft tissue, bone, and retroperitoneum. However, an...

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Published in:Thoracic cancer 2022-07, Vol.13 (14), p.2078-2081
Main Authors: Gao, Xingchen, Liu, Haiyan, Wang, Feng, Xu, Ziwei, Han, Yi, Liu, Shuku
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Liu, Haiyan
Wang, Feng
Xu, Ziwei
Han, Yi
Liu, Shuku
description Angiosarcoma is a highly malignant endothelial tumor, accounting for 1% to 2% of soft tissue sarcomas. The most common site of the disease is the skin, accounting for approximately 60% of cases, especially the skin of the head. It can also occur in soft tissue, bone, and retroperitoneum. However, angiosarcomas of the breast and chest wall are rare. Here, we report a 44‐year‐old woman who was admitted to hospital with encapsulated empyema. She was subsequently diagnosed with angiosarcomas of the breast and chest wall with tuberculous empyema. At the same time, we also reviewed the current research progress in angiosarcoma of the breast and chest wall to explore better treatment options for these patients. Angiosarcoma of breast and chest are both very rare. A 44‐year‐old woman was diagnosed with angiosarcomas of the breast and chest wall with tuberculous empyema.
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subjects angiosarcoma
Blood
Blood transfusions
Breast cancer
Cancer therapies
Case Report
Case Reports
Chemotherapy
Diabetes
Disease
empyema
General anesthesia
Hazardous materials
Hemoptysis
Hepatitis
Immunotherapy
Lymphedema
Mesothelioma
Morphology
Ostomy
Pathology
Patients
Pleural effusion
Radiation therapy
Thrombosis
Tomography
Tuberculosis
Ultrasonic imaging
title Angiosarcoma of breast and chest wall complicated with tuberculous empyema: A case report
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