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乳腺原发性黏液性囊腺癌与浸润性导管癌混合性病例报告及文献复习

Mixed primary mucinous cystadenocarcinoma and invasive ductal carcinoma of the breast: a case report and literature review.

作者信息

Zuo Chunxia, Xie Jianlan

机构信息

Department of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

出版信息

Transl Cancer Res. 2022 Dec;11(12):4455-4464. doi: 10.21037/tcr-22-1596.

Abstract

BACKGROUND

Mucinous cystadenocarcinoma (MCA) mainly occurs in the ovary, pancreas, and appendix, whereas the breast is a rare primary site of occurrence. Invasive ductal carcinoma (IDC) is the most common breast malignancy. Only 31 cases of the breast MCA have been reported in the English literature, and the coexistence of MCA and IDC in the breast are rare.

CASE DESCRIPTION

Here, we describe a 61-year-old postmenopausal woman with no family history of breast cancer or other breast-related diseases, who presented with a palpable mass in her left breast lasting for 2 months. On ultrasonography examination, the tumor was a cystic-solid lesion with clear boundary. Magnetic resonance imaging (MRI) showed a mass with low signal intensity on T1 weighted imaging and high signal intensity on T2 weighted imaging. Intraoperative frozen sections revealed metastatic tumor cells in one sentinel lymph node (1/4). She then underwent left modified radical mastectomy with axillary dissection. The post-operative pathological examination showed the tumor consisted mostly of MCA (60%), with a small proportion of intermediate-grade IDC. The MCA had a well-demarcated cystic structure with papillary projections and abundant mucoid material. The epithelium lining cystic spaces was tall columnar, with mucin-producing cells that had basally located nuclei. The degree of cytological atypia varied considerably. Axillary lymph nodes were normal (0/15). The MCA was triple-negative for estrogen receptor (ER), progesterone receptor (PR), and HER2, and positive for CK7 but negative for CK20. Through next-generation sequencing, no mutations in the and genes were identified in our case, which was not highlighted in prior cases. After surgery, the patient underwent eight cycles of chemotherapy, and she has been disease-free during the 10-month follow-up. In addition to detailing this instance of mixed MCA and IDC of the breast, we reviewed relevant literature and compare our findings with other patients who had breast MCAs.

CONCLUSIONS

Our results improved the understanding of mixed MCA and IDC, especially MCA, and provided a basis for its diagnosis and differential diagnosis from other metastatic diseases.

摘要

背景

黏液性囊腺癌(MCA)主要发生于卵巢、胰腺和阑尾,而乳腺是其罕见的原发部位。浸润性导管癌(IDC)是最常见的乳腺恶性肿瘤。英文文献中仅报道了31例乳腺MCA病例,乳腺MCA与IDC并存的情况罕见。

病例描述

在此,我们描述一名61岁的绝经后女性,她没有乳腺癌或其他乳腺相关疾病的家族史,因左侧乳房可触及肿块持续2个月前来就诊。超声检查显示肿瘤为边界清晰的囊实性病变。磁共振成像(MRI)显示肿块在T1加权成像上呈低信号强度,在T2加权成像上呈高信号强度。术中冰冻切片显示一个前哨淋巴结中有转移瘤细胞(1/4)。随后她接受了左侧改良根治性乳房切除术及腋窝淋巴结清扫术。术后病理检查显示肿瘤主要由MCA(60%)组成,伴有一小部分中级别IDC。MCA具有界限清楚的囊性结构,有乳头样突起和丰富的黏液样物质。囊腔内衬上皮为高柱状,有产生黏液的细胞,细胞核位于基底。细胞学异型程度差异很大。腋窝淋巴结正常(0/15)。该MCA雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(HER2)均为三阴性,细胞角蛋白7(CK7)阳性,细胞角蛋白20(CK20)阴性。通过二代测序,我们的病例中未发现 和 基因的突变,之前的病例中也未强调这一点。术后患者接受了8个周期的化疗,在10个月的随访期间无疾病复发。除了详细描述这例乳腺MCA与IDC混合的病例外,我们还回顾了相关文献,并将我们的发现与其他患有乳腺MCA的患者进行了比较。

结论

我们的结果增进了对MCA与IDC混合情况,尤其是MCA的认识,为其诊断及与其他转移性疾病的鉴别诊断提供了依据。

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