Defaud-Hénon Florence, Tunon-de-Lara Christine, Fournier Marion, Marty Marion, Velasco Valérie, de Mascarel Isabelle, MacGrogan Gaëtan
Université Bordeaux-2, 33000 Bordeaux, France.
Ann Pathol. 2010 Feb;30(1):7-16. doi: 10.1016/j.annpat.2010.01.003. Epub 2010 Feb 18.
Adenoid cystic carcinoma (ACC) of the Breast is a rare tumour (less than 1 % of all breast carcinomas). The aim of this study was to determine the clinical, histological and immunohistochemical characteristics of these tumours.
From the database of the Bergonié Institute of Bordeaux, 30 cases of ACC were identified. The clinical and histological features of these carcinomas were characterized. An immunohistochemical study was performed with the following antibodies: ER, PR, HER-2-neu, Vimentin, EGFR, P63, SMA, CK5/6, CK8/18, CK14, cKIT, MIB1, CD44 and CD24.
Thirty patients were included (median age 60.7 years). The 10 axillary lymph node dissections and two sentinel lymph procedures were negative. The architecture was frequently of a mixed type (26/30) and less often solid (4/30). Among the 23 patients for whom follow up was available (median follow-up: 84 months [2-288]), there were three local recurrences and three metastatic events. The tumors with recurrence and metastasis showed more necrosis, a mitotic count greater than 4/10hpf, and in one case perineural infiltration. All the tumours were ER, PR and Her-2-neu negative. Morphological and immunophenotypical analysis disclosed in each tumor, a basaloid and a luminal cell population with divergent immunophenotypical patterns.
The mammary ACC is made of two cell types and is of good prognosis despite its triple negative phenotype, similar to the basal-like infiltrating carcinoma NOS. Axillary lymph node dissection is not recommended. Good local control by at least large lumpectomy with long-term follow-up is necessary.
乳腺腺样囊性癌(ACC)是一种罕见肿瘤(占所有乳腺癌的比例不到1%)。本研究的目的是确定这些肿瘤的临床、组织学和免疫组化特征。
从波尔多贝戈涅研究所的数据库中,识别出30例ACC病例。对这些癌的临床和组织学特征进行了描述。使用以下抗体进行免疫组化研究:雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(HER-2-neu)、波形蛋白、表皮生长因子受体(EGFR)、P63、平滑肌肌动蛋白(SMA)、细胞角蛋白5/6(CK5/6)、细胞角蛋白8/18(CK8/18)、细胞角蛋白14(CK14)、干细胞生长因子受体(cKIT)、增殖细胞核抗原(MIB1)、CD44和CD24。
纳入30例患者(中位年龄60.7岁)。10例腋窝淋巴结清扫术和2例前哨淋巴结活检结果均为阴性。组织结构多为混合型(26/30),实体型较少(4/30)。在有随访资料的23例患者中(中位随访时间:84个月[2 - 288个月]),有3例局部复发和3例转移事件。复发和转移的肿瘤显示更多坏死,有丝分裂计数大于4/10高倍视野,且1例有神经周围浸润。所有肿瘤的ER, PR和Her-2-neu均为阴性。形态学和免疫表型分析显示,每个肿瘤中均存在具有不同免疫表型模式的基底样细胞群和管腔样细胞群。
乳腺ACC由两种细胞类型组成,尽管其为三阴性表型,但预后良好,类似于基底样浸润性癌(非特殊类型)。不建议行腋窝淋巴结清扫术。至少通过大肿块切除术并进行长期随访以实现良好的局部控制是必要的。