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作 者:袁静萍[1] 阎红琳 吴昊[1] 高利昆[1] 饶洁[1] 胡继昌[1] 袁修学[2]
机构地区:[1]武汉大学人民医院病理科,430060 [2]武汉科技大学基础医学院,430065
出 处:《中华内分泌外科杂志》2017年第2期107-109,126,共4页Chinese Journal of Endocrine Surgery
基 金:湖北省自然科学基金课题(2013CFB374)
摘 要:目的探讨乳腺腺样囊性癌的临床病理特征及鉴别诊断。方法收集3例乳腺腺样囊性癌的临床病理资料并随访,观察其临床病理特征和免疫表型。结果3例均为女性,平均年龄61(55~72)岁。肿块均位于乳晕旁,大体边界清楚,切面呈灰白色。肿瘤在结构上由肌上皮和腺上皮2种细胞构成筛孔型、管状小梁状型2种类型,免疫组织化学显示肌上皮细胞表达SMA、CK5/6、P63、CD117,腺上皮表达CK18、EMA、CK7。2种细胞均不表达ER、PR、HER2、CD10。结论乳腺腺样囊性癌是一种少见的乳腺肿瘤,是基底细胞亚型,但具有良好的预后。其特征性的组织形态、免疫组化表型有助于诊断和鉴别诊断。ObjectiveTo explore the clinicopathological features and diagnosis of adenoid cystic carcinoma of the breast (ACCB) .MethodsClinical data of 3 cases of ACCB were collected and followed up to observe the clinical pathological features. Immunohistochemistry was used to determine the immune phenotype.ResultsAll the 3 cases were female, aging from 55 to 72 years old (61 years old as the average) . The tumors were found in subareolar region well-circumscribed. ACCB was characterized by the presence of a dual cell population of luminal and basaloid cells arranged in cribriform and tubular-trabecular patterns. On immunohistochemical staining, the myoepithelial cells expressed SMA, CK5/6, P63, CD117 and the glandular epithelium cells were mostly positive for CK18, EMA, CK7, while no expression of ER, PR, HER-2, CD10 was observed.ConclusionsACCB is a rare neoplasm with a triple-negative, basal-like phenotype, but exhibits an indolent clinical behavior. The diagnosis can be worked out by evaluation of clinical characterstics, histological and immunohistochemical features.
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