Qin Xiaojuan, Wu Yu, Yu Lan, Lv Qing, Xie Mingxing
Department of Ultrasound, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
J Int Med Res. 2021 Mar;49(3):3000605211002337. doi: 10.1177/03000605211002337.
Primary breast angiosarcoma (PBA) is a rare malignant tumor. PBA usually undergoes hematogenous metastasis; lymph node metastasis is very rare in such patients, and metastasis of PBA to the supraclavicular lymph nodes has not previously been reported. Here, we describe a rare case of PBA manifested by a diffuse enlargement of the left breast, with metastasis to the left axillary and bilateral supraclavicular lymph nodes. Contrast-enhanced ultrasound and positron emission tomography findings indicated a malignant lesion, whereas magnetic resonance imaging suggested a benign lesion. Core needle biopsy identified the lesion as a lymphangioma, and the histological characteristics suggested a high-grade angiosarcoma. Multimodal imaging and perfusion patterns obtained using various contrast agents can thus help to diagnose PBA.
原发性乳腺血管肉瘤(PBA)是一种罕见的恶性肿瘤。PBA通常发生血行转移;此类患者发生淋巴结转移非常罕见,且此前尚未有PBA转移至锁骨上淋巴结的报道。在此,我们描述了一例罕见的PBA病例,表现为左乳弥漫性增大,并伴有左腋窝及双侧锁骨上淋巴结转移。超声造影和正电子发射断层扫描结果提示为恶性病变,而磁共振成像提示为良性病变。粗针活检将病变诊断为淋巴管瘤,但其组织学特征提示为高级别血管肉瘤。因此,使用各种造影剂获得的多模态成像和灌注模式有助于诊断PBA。