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[乳腺囊性高分泌性病变的临床病理特征]

[Clinicopathologic features of cystic hypersecretory lesion of the breast].

作者信息

Bi Rui, Cheng Yufan, Yu Baohua, Shui Ruohong, Yang Wentao, Xu Xiaoli

机构信息

Department of Pathology, Cancer Center, Fudan University; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.

Department of Pathology, Cancer Center, Fudan University; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China. E-mail:

出版信息

Zhonghua Bing Li Xue Za Zhi. 2014 Jan;43(1):25-9.

Abstract

OBJECTIVE

To study the clinicopathologic features, immunophenotype and differential diagnosis of cystic hypersecretory lesion (CHL) of the breast.

METHODS

Clinicopathologic and follow-up data of six cases of breast CHL in 2010-2013 were collected and reviewed.Immunohistochemical and mucinous staining was performed.

RESULTS

All six patients were female, age ranged from 37 to 71 years (average 49.3 years). Three cases were cystic hypersecretory hyperplasia (CHH), the other three cases were cystic hypersecretory carcinoma (CHC). Clinically the lesions presented as either breast mass or mammographic calcification.Grossly, the cystic hypersecretory lesions were poorly circumscribed, with multiple colloid containing cysts on the cut surface. Microscopically, the remarkable feature was numerous enlarged cysts which contained densely eosinophilic homogeneous secretion similar to the colloid seen in thyroid follicles, and calcification was seen in the cyst in one case. The secretion was D-PAS and mucicarmine positive. The lining epithelium of the cysts was uniformly flat, cuboid or columnar, and arranged in a monolayer. The cells may be arranged in turfs, solid or micropapillary patterns in CHH.In cases with dysplasia, the epithelium showed cytological and structural atypia, but the usual morphology of atypical dutal hyperplasia such as arcades, rigid bridges or cribriform pattern was less common. The three CHC included two invasive ductal carcinomas (IDC) and one ductal carcinoma in situ (DCIS).In CHL, there was immunoreactivity to S-100 protein, CK5/6 and CK14.Of the three CHCs, ER and PR were expressed in only one IDC.No HER2 expression was identified in the two invasive CHCs.One patient was lost to follow-up, and the rest were uneventful at 18 months.

CONCLUSIONS

CHL of the breast is a rare pathological entity. Multiple colloid-filled cysts is a unique histological feature. The epithelium of CHL may show usual hyperplasia, dysplasia or carcinoma.

摘要

目的

研究乳腺囊性高分泌性病变(CHL)的临床病理特征、免疫表型及鉴别诊断。

方法

收集并回顾2010 - 2013年6例乳腺CHL的临床病理及随访资料。进行免疫组化及黏液染色。

结果

6例均为女性,年龄37至71岁(平均49.3岁)。3例为囊性高分泌性增生(CHH),另3例为囊性高分泌性癌(CHC)。临床上病变表现为乳腺肿块或乳腺钼靶钙化。大体上,囊性高分泌性病变边界不清,切面有多个含胶体的囊肿。显微镜下,显著特征是大量扩大的囊肿,内含致密嗜酸性均质分泌物,类似于甲状腺滤泡中的胶体,1例囊肿内可见钙化。分泌物D - PAS及黏液卡红染色阳性。囊肿内衬上皮均匀为扁平、立方或柱状,呈单层排列。CHH中细胞可呈簇状、实性或微乳头样排列。有发育异常的病例,上皮显示细胞学及结构异型性,但不常见典型导管上皮增生如拱廊样、硬桥样或筛状结构等形态。3例CHC包括2例浸润性导管癌(IDC)和1例导管原位癌(DCIS)。在CHL中,S - 100蛋白、CK5/6及CK14呈免疫反应阳性。3例CHC中,仅1例IDC表达雌激素受体(ER)和孕激素受体(PR)。2例浸润性CHC均未检测到HER2表达。1例患者失访,其余患者18个月时情况良好。

结论

乳腺CHL是一种罕见的病理实体。多个含胶体的囊肿是其独特的组织学特征。CHL的上皮可表现为普通增生、发育异常或癌变。

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