A Rare Case of Post-Radiation Angiosarcoma with Pleural Metastasis

Authors

DOI:

https://doi.org/10.46570/utjms-2026-1324

Keywords:

Angiosarcoma, pleural metastsis, breast cancer

Abstract

Soft tissue sarcomas (STS) represent 1% of all malignancies in adults. Angiosarcomas are an uncommon subtype of vascular or lymphatic origin, compromising 2% of STS. We present a rare case of secondary angiosarcoma of the breast. Following treatment for invasive ductal carcinoma and subsequent diagnosis of radiation-induced angiosarcoma two years prior, a 77-year-old female presented with dyspnea and bilateral pleural effusions. Diagnostic thoracentesis demonstrated findings consistent with metastatic angiosarcoma. Angiosarcoma of the breast is exceptionally rare among soft tissue neoplasms and is typically associated with a poor prognosis.

References

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Published

2026-07-24

How to Cite

1.
Patel R, Salih A, Jame R, Maqsood A, Noori Z, Yoon Y. A Rare Case of Post-Radiation Angiosarcoma with Pleural Metastasis. Translation [Internet]. 2026 Jul. 24 [cited 2026 Jul. 26];16(1). Available from: https://openjournals.utoledo.edu/index.php/translation/article/view/1324

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Section

Case Reports