Costarelli Leopoldo, Campagna Domenico, Ascarelli Alessandra, Cavaliere Francesco, Colavito Maria Helena, Ponzani Tatiana, Broglia Laura, La Pinta Massimo, Manna Elena, Fortunato Lucio
Breast Unit, San Giovanni-Addolorata Hospital, Rome, Italy.
Breast Cancer (Dove Med Press). 2017 Dec 8;9:581-586. doi: 10.2147/BCTT.S145570. eCollection 2017.
Pleomorphic invasive lobular carcinoma (P-ILC) is an uncommon variety of invasive lobular carcinoma with aggressive clinical features. Little is described in the literature regarding this topic.
We reviewed our experiences from 2010 to 2015 and compared 40 patients with P-ILC, 126 patients with classic-ILC (C-ILC) and 574 cases of high-grade invasive ductal carcinoma (HG-IDC). We studied the histologic and immunohistochemical features, clinical presentation and surgical treatment.
P-ILC is diagnosed at the same age and tumor diameter as those of the other two histologic types. It is associated more frequently with multiple lymph node metastases and high proliferative index, and HER2/neu is amplified in 10% of cases. In spite of sharing some histologic characteristics with C-ILC (same growth pattern, loss of E-cadherin expression, same genetic pathway), its clinical and pathologic features define an autonomous entity. Its surgical treatment is similar to those of C-ILC and HG-IDC.
This is the first review comparing these three pathologic entities. Our findings may be useful in understanding this variety of invasive lobular carcinoma, and further studies are certainly needed in this field.
多形性浸润性小叶癌(P-ILC)是浸润性小叶癌的一种罕见类型,具有侵袭性临床特征。关于这一主题,文献中描述较少。
我们回顾了2010年至2015年的经验,比较了40例P-ILC患者、126例经典浸润性小叶癌(C-ILC)患者和574例高级别浸润性导管癌(HG-IDC)患者。我们研究了组织学和免疫组化特征、临床表现及手术治疗情况。
P-ILC的诊断年龄和肿瘤直径与其他两种组织学类型相同。它更常与多区域淋巴结转移和高增殖指数相关,10%的病例中HER2/neu呈扩增状态。尽管与C-ILC有一些组织学特征相同(生长方式相同、E-钙黏蛋白表达缺失、遗传途径相同),但其临床和病理特征定义了一个独立的实体。其手术治疗与C-ILC和HG-IDC相似。
这是首次对这三种病理实体进行比较的综述。我们的研究结果可能有助于理解这种浸润性小叶癌,该领域肯定需要进一步研究。