Matsubayashi Roka Namoto, Iwasaki Hiromi, Iwakuma Nobutaka, Momosaki Seiya
Breast Care Center, Department of Radiology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, Japan.
Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, Japan.
Clin Imaging. 2019 Jan-Feb;53:120-125. doi: 10.1016/j.clinimag.2018.10.004. Epub 2018 Oct 6.
Tumors originating from the nipple-areolar complex of the breast are rare. We herein report the case of a patient with metachronous bilateral areolar methotrexate (MTX)-associated lymphoma. The patient was a 67-year-old woman who presented with a rapidly enlarging tumor in the areolar region of her left breast. She had a long history of rheumatoid arthritis and had taken MTX for many years. On ultrasonography, the tumor showed well-demarcated margins and hyper-vascularity. On magnetic resonance imaging, the tumor showed a homogeneous low-to-moderate signal intensity that was similar to that of the nipple on both T1- and T2-weighted imaging; the diffusion was significantly reduced on diffusion-weighted images. The tumor showed a medium-plateau pattern on dynamic contrast-enhanced imaging. No necrotic change was observed. Based on the imaging findings, we considered the tumor to have originated from the areola. According to the internal homogeneity, the rapid growth and hyper-cellularity, the potential diagnoses included a small round cell tumor (including malignant lymphoma) and a mesenchymal neoplasm (especially leiomyoma or leiomyosarcoma, which frequently originate from the areolar region). An excisional biopsy of the tumor was performed. The pathological diagnosis was diffuse large, non GC B-cell lymphoma that we suspected was associated with MTX. The tumor shrank rapidly after the withdrawal of MTX. After three months, we detected a B-cell lymphoma of the same type originating in the contralateral areola. We compared the characteristics of the imaging findings of the MTX-associated lymphoma with the nipple-areolar or periareolar tumors and primary breast lymphoma.
起源于乳腺乳头乳晕复合体的肿瘤较为罕见。我们在此报告一例异时性双侧乳晕甲氨蝶呤(MTX)相关淋巴瘤患者的病例。该患者为一名67岁女性,其左乳房乳晕区出现一个迅速增大的肿瘤。她有类风湿关节炎病史多年,服用MTX多年。超声检查显示肿瘤边界清晰,血运丰富。磁共振成像显示,在T1加权和T2加权成像上,肿瘤呈均匀的低至中等信号强度,与乳头相似;在扩散加权图像上扩散明显降低。动态对比增强成像显示肿瘤呈中等平台模式。未观察到坏死改变。基于影像学表现,我们认为肿瘤起源于乳晕。根据内部均匀性、快速生长和细胞增多情况,可能的诊断包括小圆细胞瘤(包括恶性淋巴瘤)和间叶性肿瘤(尤其是平滑肌瘤或平滑肌肉瘤,它们常起源于乳晕区)。对肿瘤进行了切除活检。病理诊断为弥漫性大B细胞淋巴瘤,非生发中心型,我们怀疑与MTX有关。停用MTX后肿瘤迅速缩小。三个月后,我们在对侧乳晕发现了同一类型的B细胞淋巴瘤。我们将MTX相关淋巴瘤的影像学表现特征与乳头乳晕或乳晕周围肿瘤以及原发性乳腺淋巴瘤进行了比较。