Department of Pathology, University of Miami Miller School of Medicine, Jackson Memorial Hospital, FL 33136, USA.
Am J Clin Pathol. 2012 May;137(5):747-52. doi: 10.1309/AJCP5W5SEZSEHUHE.
Mammaglobin A (MG-A) is purportedly useful for detecting metastatic carcinomas suspected to be of breast origin and has been advocated as a useful marker of micrometastasis in sentinel lymph nodes and minimal residual tumor in bone marrow. Little is known about its expression frequency in histologic subtypes of breast cancer. Excisional biopsy specimens from 1,079 untreated invasive mammary carcinomas were evaluated for immunohistochemical expression of MG-A. In addition to estrogen (ER) and progesterone receptors (PR) and HER2, staining for p63 and HLA-DR was used to further characterize histologic subtypes. Of the carcinomas, 36 were classified as metaplastic (based on morphologic features, ER-/PR-/HER2-, p63+), 38 as medullary (ER-/PR-/HER2-, HLA-DR+), and 1,005 as ductal, no special type (NST). All metaplastic and medullary carcinomas were negative for MG-A. Of 1,005 ductal carcinomas, NST, 492 (49.0%) were MG-A+, 62.0% with a reaction in fewer than 25% of the cells. MG-A immunohistochemical studies failed to detect all medullary and metaplastic cancers and more than 50% of ductal carcinomas, NST. In two thirds of MG-A+ ductal carcinomas, the reaction was only focal and usually in a minority of cells. These findings suggest that MG-A has limited value in identifying the mammary origin of carcinomas, particularly in small biopsy specimens used to detect metastasis or minimal residual disease.
乳腺珠蛋白 A(MG-A)据称可用于检测疑似乳腺来源的转移性癌,并被提倡作为前哨淋巴结微转移和骨髓中微小残留肿瘤的有用标志物。关于其在乳腺癌组织学亚型中的表达频率知之甚少。对 1079 例未经治疗的浸润性乳腺腺癌的切除性活检标本进行了 MG-A 的免疫组织化学表达评估。除了雌激素(ER)和孕激素受体(PR)和 HER2 外,还使用 p63 和 HLA-DR 染色进一步表征组织学亚型。在这些癌中,36 例被归类为化生型(基于形态特征,ER-/PR-/HER2-,p63+),38 例为髓样型(ER-/PR-/HER2-,HLA-DR+),1005 例为导管型,非特殊型(NST)。所有化生型和髓样型癌均为 MG-A 阴性。在 1005 例导管癌中,NST 有 492 例(49.0%)为 MG-A+,62.0%的反应少于 25%的细胞。MG-A 免疫组化研究未能检测到所有髓样型和化生型癌,以及超过 50%的导管癌,NST。在三分之二的 MG-A+导管癌中,反应仅为局灶性,通常仅存在于少数细胞中。这些发现表明,MG-A 在识别癌的乳腺来源方面的价值有限,特别是在用于检测转移或微小残留疾病的小活检标本中。