Translational Cell and Tissue Research Laboratory, KU Leuven, Leuven, Belgium.
Department of Pathology, UZ Leuven, University Hospitals, Leuven, Belgium.
Diagn Pathol. 2023 Apr 25;18(1):52. doi: 10.1186/s13000-023-01337-5.
Breast-implant associated (BIA) lymphoma is an infrequent type of cancer occurring in the fluid and fibrous capsule around a textured breast implant. Recently, both the 2022 WHO 5th edition classification of Haematological tumours (WHO HAEM5) and 2022 International Consensus Classification of Mature Lymphoid Neoplasms (22ICC), recognized breast implant-associated Anaplastic Large Cell Lymphoma (BIA-ALCL) as a definitive entity, defined as a mature CD30-positive T-cell lymphoma, confined by a fibrous capsule, in a breast implant setting. Only few B-cell lymphomas have been reported in the literature to be associated with breast implants. Here we report two EBV-positive Diffuse Large B-cell lymphomas (EBV + DLBCL) in relation to a breast implant, both expressing CD30 as well as EBV latency type 3. Both lesions were considered as DLBCL associated with chronic inflammation (CI-DLBCL), but one presented as a 7 cm solid mass, while the other presented as a fibrin-associated DLBCL (FA-DLBCL) in an HIV patient. Clinically, both are in complete remission 6 months or longer after capsulectomy and graft removal, without additional chemotherapy.Such cases, characterized by large CD30-positive cells, can easily be misdiagnosed as BIA-ALCL if the cell of origin is not further established. Therefore, a diagnostic panel including lineage-specific B-and T-cell markers and EBER in situ hybridization is essential to recognize this rare entity, to understand lymphomagenesis, to predict outcome and to define clinical approach.
乳房植入物相关(BIA)淋巴瘤是一种罕见的癌症,发生在纹理乳房植入物周围的液体和纤维囊内。最近,2022 年世界卫生组织(WHO)第五版血液肿瘤分类(WHO HAEM5)和 2022 年国际成熟淋巴细胞肿瘤共识分类(22ICC)均将乳房植入物相关间变性大细胞淋巴瘤(BIA-ALCL)确认为一种明确的实体,定义为局限于纤维囊内的成熟 CD30 阳性 T 细胞淋巴瘤,发生在乳房植入物环境中。文献中仅报道了少数与乳房植入物相关的 B 细胞淋巴瘤。在此,我们报告了两例与乳房植入物相关的 EBV 阳性弥漫性大 B 细胞淋巴瘤(EBV+DLBCL),均表达 CD30 和 EBV 潜伏类型 3。这两个病变均被认为是与慢性炎症相关的 DLBCL(CI-DLBCL),但一个表现为 7cm 实性肿块,另一个表现为 HIV 患者中的纤维蛋白相关 DLBCL(FA-DLBCL)。临床上,在囊切除术和移植物切除后 6 个月或更长时间,这两个病例均完全缓解,无需额外化疗。如果不进一步确定起源细胞,这些特征为大的 CD30 阳性细胞的病例很容易误诊为 BIA-ALCL。因此,诊断小组包括谱系特异性 B 和 T 细胞标志物和 EBER 原位杂交对于识别这种罕见实体、了解淋巴瘤发生、预测结局和定义临床方法至关重要。