Kouhashi Rika, Kashiwagi Shinichiro, Asano Yuka, Morisaki Tamami, Ishihara Sae, Goto Wataru, Tanaka Sayaka, Kuwae Yuko, Ohsawa Masahiko, Hirakawa Kosei, Ohira Masaichi
Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Department of Gastrointestinal Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Case Rep Oncol. 2021 Mar 29;14(1):604-609. doi: 10.1159/000513906. eCollection 2021 Jan-Apr.
Angiosarcoma is a malignant mesenchymal tumor characterized by the presence of vascular endothelial cells. Although rare, angiosarcoma developing in the mammary glands has a poor prognosis. We report a case of breast angiosarcoma with a preoperative diagnosis of late recurrence of breast cancer. A 78-year-old woman noticed a tumor in her right breast and visited our hospital. The patient had undergone breast-conserving surgery and axillary lymph node dissection from the right breast 12 years before the visit. The tumor was diagnosed as T4bN0M0, stage IIIB. Anastrozole was administered as postoperative adjuvant therapy for 5 years; the patient also received 50-Gy whole-breast radiation therapy after surgery. Physical examination during her visit revealed an elevated lesion with blue purpura around the nipple in the right breast. We performed breast ultrasound and detected a well-defined 19.6 × 16.4 × 10.7 mm hypoechoic tumor in the left subareolar area. The patient underwent core needle biopsy (CNB). Based on the CNB specimen findings, she was suspected to experience late local recurrence after surgery. Therefore, she underwent total mastectomy after breast-conserving surgery. A dark-red tumor sized 18 × 12 mm was found in a specimen from the nipple. The pathological diagnosis of the specimen revealed short spindle-shaped tumor cells with strong nuclear pleomorphism and a significant interstitial fibrosis. Immunohistochemistry using D2-40 and CD31 antibodies showed irregular luminal proliferation at the anastomosis, infiltration into the surrounding tissue, and massive necrosis, thereby leading to the diagnosis of breast angiosarcoma. We have reported a case of breast angiosarcoma with a preoperative diagnosis of late recurrence of breast cancer.
血管肉瘤是一种以血管内皮细胞存在为特征的恶性间充质肿瘤。尽管罕见,但发生于乳腺的血管肉瘤预后较差。我们报告一例术前诊断为乳腺癌晚期复发的乳腺血管肉瘤病例。一名78岁女性发现右乳有肿物,遂来我院就诊。该患者在此次就诊前12年曾接受右乳保乳手术及腋窝淋巴结清扫术。肿瘤被诊断为T4bN0M0,ⅢB期。术后给予阿那曲唑辅助治疗5年;患者术后还接受了50 Gy的全乳放疗。此次就诊时体格检查发现右乳乳头周围有一隆起性病变,伴有青紫瘀斑。我们进行了乳腺超声检查,在左乳晕下区域检测到一个边界清晰的19.6×16.4×10.7 mm低回声肿瘤。患者接受了粗针穿刺活检(CNB)。根据CNB标本检查结果,怀疑她术后出现晚期局部复发。因此,她在保乳手术后接受了全乳切除术。在乳头标本中发现一个暗红色肿物,大小为18×12 mm。标本的病理诊断显示肿瘤细胞呈短梭形,核异型性强,间质纤维化明显。使用D2-40和CD31抗体进行免疫组化检查显示吻合处有不规则的管腔增生、向周围组织浸润以及大片坏死,从而确诊为乳腺血管肉瘤。我们报告了一例术前诊断为乳腺癌晚期复发的乳腺血管肉瘤病例。