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无爱泼斯坦-巴尔病毒感染的原发性乳腺伯基特淋巴瘤:一例报告及文献复习

Primary Burkitt's lymphoma of the breast without Epstein-Barr virus infection: A case report and literature review.

作者信息

Wei Jianguo, Lin Caixia, Xu Chunwei, Xi Qun, Wang Cheng

机构信息

Department of Pathology, The General Military Hospital of Beijing PLA, Beijing 100700, People's Republic of China.

出版信息

Indian J Pathol Microbiol. 2015 Oct-Dec;58(4):546-9. doi: 10.4103/0377-4929.168863.

DOI:10.4103/0377-4929.168863
PMID:26549090
Abstract

Burkitt lymphoma (BL) is a highly aggressive neoplasm, which arising from the germinal center or post germinal center B-cell. Primary breast lymphomas are extremely rare, and the most common histologic type is diffuse large B-cell lymphoma. Primary BL of the breast is much less common than the other types of lymphoma. Here, we report an extremely rare case of a 37-year-old Chinese female with localized bilateral breast, who was referred to our institution for bilateral breast swelling. The left breast tissue ultrasonography showed the short axis measuring 20.3 mm × 18.8 mm and the long axis measuring 22.1 mm × 20.8 mm soft tissue mass. The right breast tissue ultrasonography showed the short axis measuring 30.2 mm × 26.9 mm and the long axis measuring 33.5 mm × 2.18 mm. Coarse needle biopsy of breast masses demonstrated a non-Hodgkin's B-cell lymphoma. The patient underwent a bilateral mastectomy. Histological examination of the tumor showed a characteristic "starry sky" pattern, the medium-sized tumor cells were a monotonous pattern of growth, and there were many abnormal mitotic figures. The neoplastic cells strongly expressed CD20, CD79-μ, MUM-1, PAX-5, CD43 and Bcl-6, Ki-67 were nearly 100% positive, but negative for CD10, Bcl-2 and TdT. By fluorescence in situ hybridization an IGH-MYC gene fusion was detected in the tumor tissue which indicating the presence of a typical BL translocation t(8;14)(q24;q32). The final histopathological diagnosis was primary BL of the breast.

摘要

伯基特淋巴瘤(BL)是一种高度侵袭性肿瘤,起源于生发中心或生发中心后B细胞。原发性乳腺淋巴瘤极为罕见,最常见的组织学类型是弥漫性大B细胞淋巴瘤。乳腺原发性BL比其他类型的淋巴瘤更为少见。在此,我们报告一例极其罕见的37岁中国女性病例,其双侧乳腺局部出现肿胀,遂转诊至我院。左侧乳腺组织超声检查显示短轴为20.3mm×18.8mm,长轴为22.1mm×20.8mm的软组织肿块。右侧乳腺组织超声检查显示短轴为30.2mm×26.9mm,长轴为33.5mm×2.18mm。乳腺肿块粗针活检显示为非霍奇金B细胞淋巴瘤。该患者接受了双侧乳房切除术。肿瘤组织学检查显示出特征性的“星空”样图案,中等大小的肿瘤细胞呈单调生长模式,且有许多异常有丝分裂象。肿瘤细胞强烈表达CD20、CD79-μ、MUM-1、PAX-5、CD43和Bcl-6,Ki-67几乎100%呈阳性,但CD10、Bcl-2和TdT呈阴性。通过荧光原位杂交在肿瘤组织中检测到IGH-MYC基因融合,这表明存在典型的BL易位t(8;14)(q24;q32)。最终组织病理学诊断为乳腺原发性BL。

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