Multinucleated giant cell reaction in lower lip squamous cell carcinoma: a clinical, morphological, and immunohistochemical study

Background 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...

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Veröffentlicht in:Journal of oral pathology & medicine 2017-10, Vol.46 (9), p.773-779
Hauptverfasser: Santos, Hellen Bandeira de Pontes, Miguel, Márcia Cristina da Costa, Pinto, Leão Pereira, Gordón‐Núñez, Manuel Antonio, Alves, Pollianna Muniz, Nonaka, Cassiano Francisco Weege
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Sprache:eng
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Zusammenfassung:Background 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. Methods 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. Results 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). Conclusions 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.
ISSN:0904-2512
1600-0714
DOI:10.1111/jop.12565