Department of Surgery, Brooklyn Hospital Center, Brooklyn, NY, USA.
Department of Pathology, Brooklyn Hospital Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Am J Case Rep. 2024 Sep 17;25:e944755. doi: 10.12659/AJCR.944755.
BACKGROUND Amyloidosis results in fibrillar sheets of beta-pleated amorphous congophilic protein deposition in the extracellular space. Breast amyloidosis is a rare entity, with the first case reported in 1973 and only 2 major case series published since. These deposits can have local or systemic manifestations and typically present unilaterally, although bilateral involvement has been described. Some reported cases of amyloidosis have been linked to breast cancer. CASE REPORT The patient was a 60-year-old woman who presented to the breast surgery clinic for evaluation after image-guided biopsy of a right breast lesion. Core needle biopsy under stereotactic guidance demonstrated pathology consistent with nodular deposition of amyloid, associated with calcifications. Microscopic examination revealed extracellular deposition of acellular eosinophilic material in fat, stoma, and blood vessels. Congo red special stain was positive. Amyloid with Congo red special stain showed apple green birefringence under polarized light. Surgical excision under needle localization was performed, with the final surgical pathology report confirming amyloid deposits. CONCLUSIONS Breast amyloidosis can have calcium affinity, create a foreign body-like reaction with giant cell infiltration, and distribute through periductal, perivascular, or intralobar patterns. Some factors that can contribute to an increased risk or are associated with breast amyloidosis are predisposing clinical conditions, including autoimmune disease, various breast cancers, and B-cell lymphomas. Amyloidosis of the breast should be treated either as primary or secondary, based on etiology. Further studies need to be conducted on whether there are specific genetic markers that predispose populations to the development of amyloidosis of the breast.
淀粉样变性导致细胞外空间中β-折叠无定形亲刚果蛋白纤维状片层沉积。乳腺淀粉样变性是一种罕见的疾病,首例报告于 1973 年,此后仅发表了 2 项主要的病例系列。这些沉积物可具有局部或全身表现,通常单侧出现,尽管已有双侧受累的描述。一些报告的淀粉样变性病例与乳腺癌有关。
患者为 60 岁女性,因右乳病变行影像引导活检后到乳腺外科就诊。在立体定向引导下进行的空心针活检显示符合淀粉样物质结节沉积的病理学特征,伴有钙化。显微镜检查显示细胞外无定形嗜酸性物质在脂肪、窦和血管中沉积。刚果红特殊染色阳性。刚果红特殊染色的淀粉样蛋白在偏振光下显示出苹果绿双折射。在针定位下进行了手术切除,最终的手术病理报告证实了淀粉样沉积物的存在。
乳腺淀粉样变性可具有钙亲和力,产生伴有巨细胞浸润的异物样反应,并通过导管周围、血管周围或小叶内模式分布。一些可能增加风险或与乳腺淀粉样变性相关的因素包括易患临床情况,包括自身免疫性疾病、各种乳腺癌和 B 细胞淋巴瘤。乳腺淀粉样变性应根据病因作为原发性或继发性进行治疗。需要进一步研究是否存在特定的遗传标记,使某些人群易患乳腺淀粉样变性。