Article citationsMore>>

J. R. Toro, L. B. Travis, H. J. Wu, K. Zhu, C. D. M. Fletcher and S. S. Devesa, “Incidence Patterns of Soft Tissue Sarcomas, Regardless of Primary Site, in the Surveillance, Epidemiology, and End Results Program, 1978-2001: An Analysis of 26,758 Cases,” International Journal of Cancer, Vol. 119, No. 12, 2006, pp. 2922-2930. http://dx.doi.org/10.1002/ijc.22239

has been cited by the following article:

• TITLE: Angiosarcoma Following Radiation Therapy for Breast Cancer:Case Presentation and Clinical Management Considerations

  AUTHORS: Joseph R. Scalea, Branko Bojovic, Robin Legros, Julia Choi, Andrea Hebert, Nader Hanna

  KEYWORDS: Angiosarcoma; Breast Cancer; Radiation Therapy; Immunohistochemistry; TRAM Flap

  JOURNAL NAME: Open Journal of Pathology, Vol.3 No.4, October 8, 2013

  ABSTRACT: A 59-year-old woman presented with erythema and pruritis of the breast 4.5 years after undergoing lumpectomy and radiation for breast cancer. Biopsy confirmed a diagnosis of angiosarcoma. This tumor stained positive for CD34 as well as 70% Ki67 prior to therapy initiation. A multidisciplinary approach yielded a plan for neoadjuvant chemoradiation and surgical resection including delayed completion transverse rectus abdominis flap for tissue coverage. Neoadjuvant therapy successfully decreased rates of cellular proliferation, as reflected by a Ki67 of 5%, at the time of resection. Pathophysiologically, angiosarcomas may be very aggressive and may develop following radiation for breast cancer. Such tumors may become more common as breast cancer therapies, which frequently include radiation therapy, improve with time. Early recognition of angiosarcoma is imperative for successful therapy. These tumors may present with a wide range of symptoms, but may be asymptomatic. Surgical resection is the preferred therapy, but early recognition is critical.