Canas-Marques Rita, Blanca Ana, Graça-Lopes Raquel, Carvalho Inês, Pinto David G, Vasconcelos Maria Antónia, Lopez-Beltran Antonio, Fonseca Isabel
Department of Pathology.
Breast Unit, Champalimaud Foundation.
Am J Surg Pathol. 2025 Apr 1;49(4):372-380. doi: 10.1097/PAS.0000000000002361. Epub 2025 Jan 14.
E-cadherin (E-cad) immunohistochemistry is commonly used to distinguish lobular carcinoma in situ (LCIS) from ductal carcinoma in situ in histologically uncertain or ambiguous cases. Although most LCIS cases show an absence of E-cad expression on the neoplastic cell membranes, some show aberrant E-cad expression which can lead to diagnostic confusion. Awareness and understanding of the frequency, patterns, and distribution of aberrant E-cad staining in LCIS is crucial to achieving a correct diagnosis. We studied 55 LCIS cases diagnosed on core needle biopsy, classified each case by WHO subtype (classic, pleomorphic, or florid), and evaluated the frequency and patterns of aberrant E-cad expression using 3 different E-cad antibodies targeting the N-terminal (N), extracellular (EC), and C-terminal domains (C). Aberrant E-cad expression in one or more of the E-cad domains was identified in 17 cases (31%) and was significantly more frequent among LCIS variants (10/19, 56%) than among classic cases (7/36, 19.4%) ( P =0.02). Among these 17 cases, aberrant E-cad expression was seen for all 3 domains in 10 cases, for EC+C in 4, for EC+N in 2, and for N only in 1. These results indicate that about one-third of cases of LCIS can show aberrant E-cad expression, that this is more common in variants than classic types of LCIS, and that this may be seen in different E-cad domains, most often in combination. These different patterns of aberrant E-cad expression may reflect different mechanisms of E-cad alterations in LCIS, the underlying nature of which merits further studies.
在组织学诊断不明确或有歧义的病例中,E-钙黏蛋白(E-cad)免疫组化常用于区分小叶原位癌(LCIS)和导管原位癌。虽然大多数LCIS病例的肿瘤细胞膜上E-cad表达缺失,但有些病例显示E-cad表达异常,这可能导致诊断混淆。了解和认识LCIS中异常E-cad染色的频率、模式和分布对于做出正确诊断至关重要。我们研究了55例经粗针活检确诊的LCIS病例,根据世界卫生组织(WHO)亚型(经典型、多形性或小叶型)对每个病例进行分类,并使用3种针对N端(N)、细胞外(EC)和C端结构域(C)的不同E-cad抗体评估异常E-cad表达的频率和模式。在17例(31%)病例中发现一个或多个E-cad结构域存在异常E-cad表达,且在LCIS变异型(10/19,56%)中比经典型病例(7/36,19.4%)更常见(P=0.02)。在这17例病例中,10例所有3个结构域均出现异常E-cad表达,4例为EC+C结构域,2例为EC+N结构域,仅1例为N结构域。这些结果表明,约三分之一的LCIS病例可出现异常E-cad表达,在变异型中比经典型LCIS更常见,且可能出现在不同的E-cad结构域,最常见的是联合出现。这些不同模式的异常E-cad表达可能反映了LCIS中E-cad改变的不同机制,其潜在本质值得进一步研究。