Cunha Ana Luísa, Amendoeira Isabel
Department of Pathology, Hospital de S. João, Porto, Portugal.
Breast Care (Basel). 2011;6(3):227-229. doi: 10.1159/000329323. Epub 2011 Jun 14.
Breast angiosarcoma is a rare disease occurring as primary tumour or secondary to lymphoedema or radiotherapy. The more frequent use of breast-conserving therapy and radiotherapy for breast carcinoma explains the increasing diagnosis of these tumours. CASE REPORT: We report a case of a breast epithelioid angiosarcoma which metastasized to the contralateral axillary lymph node, occurring 4 years after breast-conserving therapy with axillary lymph node dissection and radiotherapy. The patient presented skin lesions and an axillary lump (clinically diagnosed as carcinoma relapse and lymph node metastasis). Fine-needle cytology on both lesions and a core needle biopsy of the axillary lump were carried out. Differential diagnosis included carcinoma, malignant melanoma, and angiosarcoma. Immunohistochemistry confirmed the diagnosis of angiosarcoma. CONCLUSIONS: Breast angiosarcoma is a challenge - clinically, radiologically and pathologically - and requires a high index of suspicion in susceptible patients.
乳腺血管肉瘤是一种罕见疾病,可作为原发性肿瘤出现,或继发于淋巴水肿或放疗。乳腺癌保乳治疗和放疗的更频繁使用解释了这些肿瘤诊断率的上升。病例报告:我们报告一例乳腺上皮样血管肉瘤病例,该病例在保乳治疗加腋窝淋巴结清扫和放疗4年后转移至对侧腋窝淋巴结。患者出现皮肤病变和腋窝肿块(临床诊断为癌复发和淋巴结转移)。对两个病变部位进行了细针穿刺细胞学检查,并对腋窝肿块进行了粗针活检。鉴别诊断包括癌、恶性黑色素瘤和血管肉瘤。免疫组化确诊为血管肉瘤。结论:乳腺血管肉瘤在临床、放射学和病理学方面都是一个挑战,在易感患者中需要高度怀疑。