Primary Breast Angiosarcoma: Serial Cases

Authors

  • Benny Gunawan Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  • Yohana Azhar Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  • Monty P. Soemitro Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  • Maman Abdurahman Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  • Kiki A. Rizky Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  • Bethy Hernowo Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Anatomical Pathology, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia

DOI:

https://doi.org/10.37275/bsm.v8i6.1016

Keywords:

Breast angiosarcoma, Histopathology, Immunohistochemistry

Abstract

Background: Breast angiosarcoma is a rare malignancy arising from endothelial cell lining, approximately 0.04–0.05% of all breast malignancies and less than 1% of all sarcomas. Consisting of primary breast angiosarcoma (PAS) and secondary breast angiosarcoma (SAS). Diagnosis is often delayed because the case is rare and asymptomatic, the lump is painless, grows quickly, progressive disease can develop distant metastasize, and the prognosis is reportedly poor.

Case presentation: This case series presents two cases of primary breast angiosarcoma; the first patient is a patient who needs to obtain a diagnosis through physical examination, imaging, surgery, histopathology, and immunohistochemistry. The second patient is how to reconstruct the surgical defect using the Latissimus dorsi flap, and interestingly, with thirteen years of survival without recurrence, Surgery is the main treatment with high local recurrence. Wide excision in the form of a simple mastectomy is recommended if a tumor-free margin of 2-3 cm cannot be achieved. Tumor excision, or cosmesis, is not achieved, which is related to the proportion of breast and tumor size. The use of radiation therapy and neoadjuvant or adjuvant chemotherapy is still controversial.

Conclusion: Establishing a diagnosis with a thorough examination starts with anamnesis, physical examination, radiological examination, and histopathology, including immunohistochemistry, which is an important examination in confirming the diagnosis.

Authors

  • Benny Gunawan1*
  • Yohana Azhar1
  • Monty P. Soemitro1
  • Maman Abdurahman1
  • Kiki A. Rizky1
  • Bethy Hernowo2
  1. 1Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Surgery, Surgical Oncology Division, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
  2. 2Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia/Department of Anatomical Pathology, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia

Corresponding author Benny Gunawan — benny.gunawan.ben@gmail.com

Article history

  1. Submitted
  2. Accepted
  3. Published

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Published

2024-04-04

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How to Cite

1.
Gunawan B, Yohana Azhar, Monty P. Soemitro, Maman Abdurahman, Kiki A. Rizky, Bethy Hernowo. Primary Breast Angiosarcoma: Serial Cases. Bioscmed [Internet]. 2024 Apr. 4 [cited 2026 Aug. 7];8(6):4529-38. Available from: https://bioscmed.com/index.php/bsm/article/view/1016

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