Topalovski M, Crisan D, Mattson J C
Pathology and Laboratory Medicine Service, Department of Veterans' Affairs Medical Center, Kansas City, MO, USA.
Arch Pathol Lab Med. 1999 Dec;123(12):1208-18. doi: 10.5858/1999-123-1208-LOTB.
Primary lymphomas of the breast are rare, accounting for 1.7% to 2.2% of extranodal lymphomas and 0.38% to 0.7% of all non-Hodgkin lymphomas. Although secondary breast lymphomas are also rare, they represent the largest group of metastatic tumors of the breast.
To investigate the clinicopathologic and immunophenotypic characteristics of breast lymphomas, the relative frequency of primary and secondary mammary lymphomas, and in selected cases, the role of gene rearrangement analysis in diagnosis and staging of these lymphomas.
We conducted a retrospective review of 22 cases of breast lymphoma diagnosed at William Beaumont Hospital, Royal Oak, Mich, during a 30-year period (1963-1994). Eleven of the 22 cases fulfilled the criteria for primary breast lymphoma; these cases represented 0.6% of all non-Hodgkin lymphomas seen in our hospital. Of the 11 cases, 5 were diffuse large B-cell lymphomas, 2 were follicle center lymphomas, 2 were marginal zone B-cell lymphomas (mucosa-associated lymphoid tissue type), 1 was a lymphoplasmacytoid lymphoma, and 1 was a peripheral B-cell neoplasm, unclassified. Using a panel of immunohistochemical stains (CD45RO, CD45RA, CD43, CD3, CD20, CD30, CD68, and HLA-DR), 8 cases demonstrated unequivocal B-cell phenotype and 3 cases had equivocal or weak staining patterns for B-cell markers. We identified no cases of T-cell lymphoma. Of 7 cases that had bone marrow biopsies for staging, 3 were positive morphologically for bone marrow involvement. Molecular analysis of B- and T-cell gene rearrangement was used to exclude bone marrow involvement in one case with bone marrow lymphoid aggregates and to confirm negativity in a case that was morphologically negative. Of the 11 secondary breast lymphomas, 5 were diffuse large B-cell lymphomas; 1 was diffuse large B-cell, primary mediastinal subtype; and 5 were follicle center lymphomas.
Breast lymphomas represented 1.2% of all non-Hodgkin lymphomas in this study; the frequency of primary and secondary cases was equal. In both groups, right breast lesions were predominant, and the most frequent morphologic type was diffuse large B-cell lymphoma. Gene rearrangement analysis is helpful in selected cases to rule out bone marrow involvement, especially in older patients, in whom lymphoid aggregates are common.
原发性乳腺淋巴瘤罕见,占结外淋巴瘤的1.7%至2.2%,占所有非霍奇金淋巴瘤的0.38%至0.7%。虽然继发性乳腺淋巴瘤也很罕见,但它们是乳腺转移性肿瘤中最大的一组。
研究乳腺淋巴瘤的临床病理和免疫表型特征、原发性和继发性乳腺淋巴瘤的相对发生率,以及在部分病例中基因重排分析在这些淋巴瘤诊断和分期中的作用。
我们对密歇根州皇家橡树市威廉·博蒙特医院在30年期间(1963 - 1994年)诊断的22例乳腺淋巴瘤进行了回顾性研究。22例中有11例符合原发性乳腺淋巴瘤的标准;这些病例占我院所见所有非霍奇金淋巴瘤的0.6%。在这11例中,5例为弥漫性大B细胞淋巴瘤,2例为滤泡中心淋巴瘤,2例为边缘区B细胞淋巴瘤(黏膜相关淋巴组织型),1例为淋巴浆细胞样淋巴瘤,1例为未分类的外周B细胞肿瘤。使用一组免疫组化染色(CD45RO、CD45RA、CD43、CD3、CD20、CD30、CD68和HLA - DR),8例显示明确的B细胞表型,3例B细胞标志物染色不明确或较弱。我们未发现T细胞淋巴瘤病例。在7例行骨髓活检以进行分期的病例中,3例骨髓形态学检查显示有骨髓受累。对B细胞和T细胞基因重排进行分子分析,用于排除1例有骨髓淋巴样聚集的病例的骨髓受累情况,并确认1例形态学检查为阴性的病例为阴性。在11例继发性乳腺淋巴瘤中,5例为弥漫性大B细胞淋巴瘤;1例为弥漫性大B细胞淋巴瘤,原发性纵隔亚型;5例为滤泡中心淋巴瘤。
在本研究中,乳腺淋巴瘤占所有非霍奇金淋巴瘤的1.2%;原发性和继发性病例的发生率相等。在两组中,右乳病变为主,最常见的形态学类型为弥漫性大B细胞淋巴瘤。基因重排分析在部分病例中有助于排除骨髓受累,特别是在老年患者中,因为淋巴样聚集很常见。