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J Thorac Cardiovasc Surg 2007;134:1076-1077
© 2007 The American Association for Thoracic Surgery
Brief Communication |
Department of Surgery, University of Illinois College of Medicine, Peoria, Peoria, Ill.
Received for publication March 8, 2007; accepted for publication April 23, 2007. * Address for reprints: Neil D. Saunders, 3602 N Kingston Dr, Apt 37, Peoria, IL 61604. (Email: neilsaunders{at}gmail.com).
Primary angiosarcomas of the breast or chest wall are exceedingly rare. Generally, primary sarcomas of the breast are less than 0.1% of breast malignancies, with angiosarcomas making up between 25% and 40% of these cases.1
Angiosarcomas tend to be aggressive, with a high rate of local recurrence and low 5- and 10-year survival rates. Standard treatment for breast or chest wall angiosarcoma is surgical excision, and there is no clear evidence regarding the role of adjuvant chemotherapy or radiation.2
Both irradiation and postmastectomy angioedema are known to substantially increase the risk for angiosarcoma in the breast or chest wall. However, the case we present is primary angiosarcoma in a radiation-naive, augmented breast.
A 58-year-old woman presented with a 4-month history of nonproductive cough and tenderness on the left side of her chest. The patient received bilateral submuscular silicone breast implants in 1975 and had noted that recently the superior aspect of her left breast had become larger than the right. On physical examination, left breast asymmetry was apparent and caused by a firm nonmobile mass. A computed tomographic (CT) scan showed a lobulated mass posterior to her left breast implant measuring 5 x 4 cm, eroding the third and fourth ribs and extending into the chest (Figure 1). Moderately prominent axillary lymph nodes were also noted. Positron emission tomographic scanning revealed no evidence of spread beyond the anterior left chest wall. Fine-needle aspiration of the mass was pankeratin positive and negative for S100, melanin A, and HMB-45 and was concluded to be non–small cell carcinoma.
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For the past 60 years, it has been known that implanted materials can induce inflammation, blood vessel proliferation, and the eventual development of angiosarcoma. In addition to those in animal models, there have been around a dozen cases of angiosarcoma associated with implanted foreign materials, including Dacron aortic grafts, dialysis shunts, and orthopedic implants.3
Commonalities among them are long latency periods and high grades at presentation, which is consistent with our case.
Multiple cohort and case-control studies of women with silicone breast implants have shown that implants do not increase ones overall cancer risk, and in many studies the breast cancer rate among women with breast implants is actually lower because of lifestyle variables in women who seek cosmetic surgery.4
The types of cancers, sarcoma versus carcinoma, are not broken down in these cohorts, and therefore it is impossible to conclude whether there is an increase in a particular type of cancer. Analysis of the Surveillance Epidemiology and End Results (SEER) data between 1973 and 1990 showed no increase in angiosarcoma in women; however, these data included all women and not just women who received silicone breast implants.5
The rarity of primary angiosarcoma suggests that even if there was a multifold increase in this cancer among women with breast implants, the resulting data would not have enough power to show a statistically significant change. The miniscule incidence of this particular cancer, including a possible increase caused by implanted materials, would not affect overall breast cancer rates but is a complication of which clinicians should be aware.
Footnotes
* Gore-Tex patch, registered trademark of W. L. Gore & Associates, Inc, Newark, Del. ![]()
References
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