Mucoepidermoid Carcinoma of the Breast: A Systematic Review of Clinicopathologic, Immunohistochemical, and Molecular Features.

IF 2.5 3区 医学 Q2 SURGERY
World Journal of Surgery Pub Date : 2025-10-01 Epub Date: 2025-09-01 DOI:10.1002/wjs.70077
Sami Akbulut, Yasin Dalda, Mariia Ivanova, Nicola Fusco
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引用次数: 0

Abstract

Background: Mucoepidermoid carcinoma (MEC) of the breast is a very rare salivary gland-like tumor, accounting for 0.2%-0.3% of all breast cancers (BC). This study aims to review the literature on MEC of the breast.

Methods: This systematic review focuses on MEC of the breast, conducted in line with PRISMA 2020 guidelines and registered in PROSPERO under ID CRD420251089598. Searches were performed in PubMed, Medline, Scopus, Web of Science, and Google Scholar, using terms such as "mucoepidermoid carcinoma," "breast," and similar terms. No language restrictions were applied. Studies published between January 1, 1979, and July 1, 2025, were included.

Results: Median age was 57 years (95% CI: 53-60). The most common presentation was a palpable breast mass (64.7%), followed by incidental detection via mammography (10.6%). Tumors were located in the left breast (49.4%) and in the right breast (43.5%). The most frequent tumor localization was the upper-outer quadrant (20.0%). Median tumor size was 21 mm (95% CI: 19-30). Modified radical mastectomy (30.6%) was the most common surgical approach, followed by breast-conserving surgery with sentinel or level dissection (29.4%), and simple mastectomy or its variants (17.6%). Immunohistochemistry revealed positivity for P63 (52.9%), CK5/6 (41.2%), CK7 (45.9%), Ki67 (44.7%), ER (24.7%), PR (4.7%), and HER2 (9.4%) with TNBC phenotype (36.5%), genetic alterations (16.5%), and distant metastasis (9.4%). Follow-up data revealed 7 deaths, of which 5 were due to MEC, and these five patients consistently exhibited poor prognostic features. Compared to the 63 survivors with follow-up data, they showed significantly higher rates of axillary lymph node positivity (p = 0.005) and advanced N stage (p = 0.001); in addition, all five had high-grade tumors (p = 0.001) and documented distant metastases (p < 0.001).

Conclusion: Breast MEC is a rare malignancy with generally favorable prognosis in low-grade cases, but high-grade tumors show more aggressive behavior. In this study, all disease-related deaths occurred in high-grade tumors with axillary node involvement, advanced N stage, and distant metastasis-highlighting their prognostic significance. CK5/6, CK7, and P63 were frequently positive, whereas hormone receptors were usually negative. Close follow-up is essential, especially for high-grade tumors.

Review registration: This systematic review was prospectively registered in the PROSPERO database under the registration number CRD420251089598.

乳腺粘液表皮样癌:临床病理、免疫组织化学和分子特征的系统综述。
背景:乳腺粘液表皮样癌(MEC)是一种非常罕见的涎腺样肿瘤,占所有乳腺癌(BC)的0.2%-0.3%。本研究旨在回顾有关乳腺MEC的文献。方法:本系统评价的重点是乳房MEC,按照PRISMA 2020指南进行,并在PROSPERO注册,编号为CRD420251089598。在PubMed, Medline, Scopus, Web of Science和谷歌Scholar中进行搜索,使用诸如“粘液表皮样癌”,“乳房”和类似的术语。没有语言限制。在1979年1月1日至2025年7月1日期间发表的研究被纳入其中。结果:中位年龄为57岁(95% CI: 53-60)。最常见的表现是可触及的乳房肿块(64.7%),其次是通过乳房x光检查偶然发现(10.6%)。肿瘤位于左乳(49.4%)和右乳(43.5%)。最常见的肿瘤定位是上外象限(20.0%)。中位肿瘤大小为21 mm (95% CI: 19-30)。改良根治性乳房切除术(30.6%)是最常见的手术方式,其次是保乳手术伴前哨或水平清扫(29.4%)和单纯乳房切除术或其变体(17.6%)。免疫组化显示P63(52.9%)、CK5/6(41.2%)、CK7(45.9%)、Ki67(44.7%)、ER(24.7%)、PR(4.7%)和HER2(9.4%)阳性,伴有TNBC表型(36.5%)、遗传改变(16.5%)和远处转移(9.4%)。随访数据显示7例死亡,其中5例为MEC,这5例患者均表现出不良预后特征。与63名有随访数据的幸存者相比,他们的腋窝淋巴结阳性(p = 0.005)和N期晚期(p = 0.001)的比例明显更高;结论:乳腺MEC是一种罕见的恶性肿瘤,在低级别病例中预后良好,但高级别肿瘤表现出更强的侵袭性行为。在这项研究中,所有与疾病相关的死亡都发生在高级别肿瘤中,包括腋窝淋巴结累及、N期晚期和远处转移,这突出了它们的预后意义。CK5/6、CK7和P63常呈阳性,而激素受体常呈阴性。密切随访是必要的,特别是对于高级别肿瘤。综述注册:本系统综述在PROSPERO数据库中前瞻性注册,注册号为CRD420251089598。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Surgery
World Journal of Surgery 医学-外科
CiteScore
5.10
自引率
3.80%
发文量
460
审稿时长
3 months
期刊介绍: World Journal of Surgery is the official publication of the International Society of Surgery/Societe Internationale de Chirurgie (iss-sic.com). Under the editorship of Dr. Julie Ann Sosa, World Journal of Surgery provides an in-depth, international forum for the most authoritative information on major clinical problems in the fields of clinical and experimental surgery, surgical education, and socioeconomic aspects of surgical care. Contributions are reviewed and selected by a group of distinguished surgeons from across the world who make up the Editorial Board.
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