Section of Anatomic Pathology, Department of Translational Research, University of Pisa, 56124, Pisa, Italy.
Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Comprehensive Cancer Center (CCC) Erlangen-EMN, 91054, Erlangen, Germany.
Virchows Arch. 2024 May;484(5):799-806. doi: 10.1007/s00428-024-03770-3. Epub 2024 Feb 26.
The diagnosis of head and neck spindle cell squamous carcinoma (SC-SCC) is often challenging. Lesions with a prominent inflammatory infiltrate and reactive vessels may have a granulation tissue-like appearance, therefore being difficult to distinguish from reactive lesions, like contact ulcers, post-intubation granulomas, inflammatory pseudotumors, or benign vascular lesions. In this study, we analyzed the clinicopathological features of a series of 17 head and neck SC-SCC with granulation tissue-like appearance. All patients, but two, were males, ranging in age between 57 and 80 years. The larynx was the most frequently affected site (n = 12), followed by the tongue (n = 4). One tumor was hypopharyngeal. Most consult cases were submitted with benign suggestion or because of unexpected recurrences of granulation tissue polyps. Histologically, all lesions consisted of an ulcerated polypoid proliferation of moderately to markedly atypical spindle cells, with a minor component of conventional invasive or in situ squamous carcinoma. At least one cytokeratin cocktail was positive in 13 cases. The staining was limited to a few neoplastic cells in most cases. Positivity for p63, p40, and cytokeratins 5/6 was detected only in the conventional squamous cell carcinoma component, when present. ALK1 was negative in all cases. Sixteen cases were tested for p53 and all showed aberrant expression (12 diffusely positive and 4 of null-phenotype). The diagnosis of granulation tissue-like SC-SCC is challenging due to the close clinical and histological overlap with several benign conditions. Since the expression of epithelial markers is limited, the use of an immunohistochemical panel including p53 is recommended.
头颈部梭形细胞鳞状细胞癌 (SC-SCC) 的诊断常常具有挑战性。具有显著炎症浸润和反应性血管的病变可能具有类似于肉芽组织的外观,因此难以与反应性病变(如接触性溃疡、插管后肉芽肿、炎性假瘤或良性血管病变)相区分。在这项研究中,我们分析了 17 例具有类似于肉芽组织外观的头颈部 SC-SCC 的临床病理特征。除了两名患者外,所有患者均为男性,年龄在 57 岁至 80 岁之间。喉部是最常受影响的部位(n=12),其次是舌(n=4)。一个肿瘤位于下咽。大多数会诊病例是因为良性建议或意外复发的肉芽组织息肉而提交的。组织学上,所有病变均由中度至明显异型性梭形细胞组成的溃疡息肉样增生,伴有少量常规浸润性或原位鳞状细胞癌。在 13 例中至少有一种细胞角蛋白鸡尾酒呈阳性。在大多数情况下,染色仅限于少数肿瘤细胞。p63、p40 和细胞角蛋白 5/6 的阳性表达仅在存在常规鳞状细胞癌成分时才能检测到。所有病例的 ALK1 均为阴性。16 例进行了 p53 检测,所有病例均显示异常表达(12 例弥漫阳性,4 例无表型)。由于与几种良性疾病的临床和组织学重叠密切,因此诊断类似于肉芽组织的 SC-SCC 具有挑战性。由于上皮标志物的表达有限,建议使用包括 p53 在内的免疫组织化学组合进行检测。