Primary Cutaneous Angiosarcoma of the Breast After Breast Trauma

Primary angiosarcoma of the breast is a rare malignant tumor. We report a case of breast primary cutaneous angiosarcoma in a patient with a strong family history of malignancy. For definitive diagnosis, a tissue biopsy is needed, with immunostaining for the presence of blood vessel endothelial markers CD31 and CD34. Total mastectomy is the preferred method of surgical treatment. Chemotherapy has not been shown to increase overall survival, but in some instances it may improve local control and disease-free survival. Surgery combined with radiation may increase local control, but patients at high risk of recurrence may benefit from adjuvant treatment as well. We discuss the potential benefits from various treatments for primary cutaneous breast angiosarcoma.

[1]  J. Hogue,et al.  Primary Breast Angiosarcoma: Avoiding a Common Trap , 2011, Case reports in oncological medicine.

[2]  D. Malkin Li-fraumeni syndrome. , 2001, Genes & cancer.

[3]  K. Syrigos,et al.  Breast angiosarcoma that is not related to radiation exposure: A comprehensive review of the literature , 2011, Surgery Today.

[4]  O. Tawfik,et al.  Angiosarcoma of the breast: a clinicopathologic analysis of cases from the last 10 years. , 2009, Annals of diagnostic pathology.

[5]  Richard C. E. Anderson,et al.  A case of chest wall angiosarcoma associated with breast implants. , 2007, The Journal of thoracic and cardiovascular surgery.

[6]  W. Woodward,et al.  Primary angiosarcomas of the breast , 2007, Cancer.

[7]  K. Hunt,et al.  Mammary angiosarcomas: imaging findings in 24 patients. , 2007, Radiology.

[8]  J. Coindre Grading of soft tissue sarcomas: review and update. , 2009, Archives of pathology & laboratory medicine.

[9]  P. Canney,et al.  Radiation-induced angiosarcoma of the breast shows major response to docetaxel after failure of anthracycline-based chemotherapy. , 2006, Breast.

[10]  S. Rossi,et al.  Angiosarcoma after breast‐conserving therapy: Fine‐needle aspiration biopsy, immunocytochemistry, and clinicopathologic correlates , 2005, Cancer.

[11]  A. Bockisch,et al.  Diagnosis of a cardiac angiosarcoma by fluorine-18 fluordeoxyglucose positron emission tomography , 2002, European Radiology.

[12]  R. Severson,et al.  Sarcoma as a second malignancy after treatment for breast cancer. , 2002, International journal of radiation oncology, biology, physics.

[13]  B. de León-Bojorge,et al.  [Breast angiosarcoma in a patient with multiple surgical procedures and breast implant. Report of a case]. , 2002, Ginecología y Obstetricia de México.

[14]  W. Mackillop,et al.  Increased risk of soft tissue sarcoma after radiotherapy in women with breast carcinoma , 2001, Cancer.

[15]  J. Birch The Li‐Fraumeni cancer family syndrome , 1990, The Journal of pathology.

[16]  P. Rosen,et al.  Mammary angiosarcoma: The prognostic significance of tumor differentiation , 1988, Cancer.

[17]  C. Fiévez,et al.  [Angiosarcoma of the breast]. , 1984, Annales de dermatologie et de venereologie.

[18]  H. Taylor,et al.  Hemangiosarcoma of the breast , 1965, Cancer.