Department of Dental Medicine, Faculty of Medicine and Pharmacy, University of Oradea, Romania;
Rom J Morphol Embryol. 2022 Apr-Jun;63(2):407-411. doi: 10.47162/RJME.63.2.11.
Head and neck squamous cell carcinoma (HNSCC) is one of the most frequent and aggressive neoplasms of this anatomical region. Many studies evaluated the neoplastic cells, but few works focused on the tumor microenvironment. In the present study, we investigated the distribution and mast cell density (MCD) in malignant and premalignant lesions of the oral cavity, tongue, pharynx, and larynx. There were analyzed 52 specimens of HNSCC, and 15 biopsies taken from patients with dysplasia. Results were compared with those found in a control group of 10 biopsies of oral mucosa from patients with inflammatory diseases. Slides stained with Hematoxylin-Eosin were used for the histopathological diagnosis and grade, and mast cells (MCs) were identified by immunohistochemistry, using anti-MC tryptase. MCs were counted using a method similar to that proposed for microvessel density. We found a significant increase in the number of MCs from the normal oral mucosa until overt carcinoma. Unlike normal tissues, in HNSCC, many MCs were found between tumor cells. We found no relationship between MCs and blood vessels in the tumor area. A significant statistical correlation was found between dysplastic and malignant tumors, but not between tumors with a different grade. Also, it was not found relationship between MCD and the anatomical location of the tumor. Based on these results, we believe that MCD evaluated by anti-MC tryptase is an independent factor of prognosis and reflects an unfavorable outcome.
头颈部鳞状细胞癌(HNSCC)是该解剖区域最常见和侵袭性的肿瘤之一。许多研究评估了肿瘤细胞,但很少有研究关注肿瘤微环境。在本研究中,我们调查了口腔、舌、咽和喉的恶性和癌前病变中的分布和肥大细胞密度(MCD)。分析了 52 例 HNSCC 标本和 15 例来自发育不良患者的活检标本。结果与来自炎症性疾病患者的口腔粘膜 10 例活检的对照组进行了比较。用苏木精-伊红染色的切片进行组织病理学诊断和分级,并用抗 MC 胰蛋白酶的免疫组织化学鉴定肥大细胞(MCs)。使用类似于微血管密度的方法对 MC 进行计数。我们发现从正常口腔粘膜到明显的癌,MC 数量显著增加。与正常组织不同,在 HNSCC 中,许多 MC 存在于肿瘤细胞之间。我们在肿瘤区域未发现 MCs 与血管之间的关系。在发育不良和恶性肿瘤之间发现了显著的统计学相关性,但在不同分级的肿瘤之间没有发现相关性。此外,MCD 与肿瘤的解剖位置之间也没有发现关系。基于这些结果,我们认为抗 MC 胰蛋白酶评估的 MCD 是预后的独立因素,反映了不良的结果。