Postgraduate Program in Dentistry, State University of Paraíba, Campina Grande, PB, Brazil.
Postgraduate Program in Oral Pathology, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
J Oral Pathol Med. 2017 Oct;46(9):773-779. doi: 10.1111/jop.12565. Epub 2017 Mar 8.
Multinucleated giant cell (MGC) reactions have been identified in several malignancies, but their frequency and significance in lower lip squamous cell carcinoma (SCC) are not established. This study evaluated the MGC reactions and their association with clinicopathological parameters in lower lip SCCs. The polarization profile of these cells (M1 or M2 macrophages) was also assessed.
The presence and distribution of MGC reactions in high-power fields (400×) were evaluated in hematoxylin/eosin-stained histological sections of 91 lower lip SCCs. The histopathological grade of malignancy was evaluated using two grading systems (World Health Organization [WHO] and Malignancy Grading of the Deep Invasive Margins). The histiocytic nature (CD68) and polarization profile (M1-HLA-DR+ or M2-CD163+) of MGCs were evaluated by immunohistochemistry.
Multinucleated giant cell reaction was identified in 36 (39.6%) cases, and its frequency was 3.3 times higher in well/moderately differentiated tumors than in poorly differentiated tumors (WHO grading system) (P = 0.006). For Malignancy Grading of the Deep Invasive Margins, the frequency was 2.03 times higher in highly/moderately keratinized tumors than in tumors with minimal/no keratinization (P = 0.012). No significant associations were observed between the presence/distribution of MGCs and clinical parameters (tumor size, lymph node metastasis, distant metastasis, and clinical stage) (P > 0.05). All MGCs were positive for CD68 and there was a predominance of HLA-DR over CD163 MGCs (P = 0.031).
Multinucleated giant cell reactions may not be involved in tumor progression in lower lip SCCs. In this microenvironment, MGCs tend to exhibit a predominantly M1 phenotype and may represent a foreign body reaction to SCC keratin pearls.
多核巨细胞(MGC)反应已在多种恶性肿瘤中被发现,但它们在下唇鳞状细胞癌(SCC)中的频率和意义尚未确定。本研究评估了 MGC 反应及其与下唇 SCC 临床病理参数的关系。还评估了这些细胞的极化特征(M1 或 M2 巨噬细胞)。
在 91 例下唇 SCC 的苏木精-伊红染色组织切片中,评估高倍视野(400×)中 MGC 反应的存在和分布。使用两种分级系统(世界卫生组织[WHO]和深部浸润边缘恶性分级)评估恶性程度。通过免疫组织化学评估 MGC 的组织细胞性质(CD68)和极化特征(M1-HLA-DR+或 M2-CD163+)。
36 例(39.6%)病例中存在多核巨细胞反应,其在中/高分化肿瘤中的频率明显高于低分化肿瘤(WHO 分级系统)(P=0.006)。对于深部浸润边缘恶性分级,高度/中度角化肿瘤中的频率明显高于最小/无角化肿瘤(P=0.012)。MGC 的存在/分布与临床参数(肿瘤大小、淋巴结转移、远处转移和临床分期)之间无显著相关性(P>0.05)。所有 MGC 均对 CD68 呈阳性,且 HLA-DR 阳性的 MGC 明显多于 CD163 阳性的 MGC(P=0.031)。
多核巨细胞反应可能不参与下唇 SCC 的肿瘤进展。在这种微环境中,MGC 倾向于表现出主要的 M1 表型,可能代表对 SCC 角蛋白珠的异物反应。