Bolin D J, Lukas G M
Kalamazoo Center for Medical Studies, Michigan State University, Michigan, USA.
Am Surg. 1996 Aug;62(8):668-72.
Dermal angiosarcoma is a rare complication of radiotherapy. It is characterized by an aggressive nature and is distinct from other forms of angiosarcoma in that it does not always present with chronic lymphedema. A few case reports have appeared of cutaneous angiosarcoma arising in women previously treated with breast-conserving treatment and radiation for breast cancer. A review of the literature reveals that these lesions are difficult to diagnose because of their rarity and their highly variable and benign appearance, which may mimic radiation-induced changes in the skin. The majority of the literature reports describe high-grade lesions; only one case of low-grade angiosarcoma was described. We now report a second case of low-grade angiosarcoma arising 10 years after segmental mastectomy, axillary lymph node dissection, and radiation treatment for infiltrating ductal carcinoma. The prompt diagnosis of dermal angiosarcoma is strongly dependent upon a high index of suspicion. Biopsy should be considered in patients who present with new skin lesions after radiation treatment for breast cancer.
皮肤血管肉瘤是放射治疗的一种罕见并发症。其特点是具有侵袭性,与其他形式的血管肉瘤不同,它并不总是伴有慢性淋巴水肿。已有一些病例报告称,曾接受保乳治疗和乳腺癌放疗的女性发生了皮肤血管肉瘤。文献综述显示,由于这些病变罕见且外观高度可变且呈良性,可能会模仿皮肤的辐射诱导变化,因此难以诊断。大多数文献报告描述的是高级别病变;仅描述了一例低级别血管肉瘤。我们现报告第二例低级别血管肉瘤,该病例发生在因浸润性导管癌行乳房部分切除术、腋窝淋巴结清扫术及放疗10年后。皮肤血管肉瘤的及时诊断强烈依赖于高度的怀疑指数。对于乳腺癌放疗后出现新皮肤病变的患者,应考虑进行活检。