Vertse Gergely, Svastics Egon, Iványi András
Fovárosi Onkormányzat Károlyi Sándor Kórház és Rendelointézet Altalános Sebészeti Osztály 1041 Budapest Nyár u. 103.
Magy Seb. 2010 Aug;63(4):164-7. doi: 10.1556/MaSeb.63.2010.4.4.
Although secondary angiosarcomas (AS) are relatively rare neoplasms, they are increasingly recognized as the result of more breast conserving therapy (BCT) followed by radiotherapy. The diagnosis of this very aggressive and rapidly spreading tumour is based on the immunohystochemical characteristics of the biopsy specimen. Only radical surgical intervention can provide successful treatment. Authors present a case of a 56-y-old woman who underwent BCT and radiotherapy. 10 years later secondary AS occurred in the remaining breast.
尽管继发性血管肉瘤(AS)是相对罕见的肿瘤,但随着越来越多的保乳治疗(BCT)后接着进行放疗,它们越来越多地被认识到。这种极具侵袭性且迅速扩散的肿瘤的诊断基于活检标本的免疫组织化学特征。只有根治性手术干预才能提供成功的治疗。作者介绍了一例56岁女性的病例,该女性接受了保乳治疗和放疗。10年后,剩余乳房发生了继发性血管肉瘤。