Department of Otolaryngology, University of Texas Medical Branch, Galveston, Texas, USA.
School of Medicine, University of Texas Medical Branch, Galveston, Texas, USA.
Cancer Rep (Hoboken). 2022 Sep;5(9):e1615. doi: 10.1002/cnr2.1615. Epub 2022 Mar 14.
Tonsillar squamous cell carcinoma (TSCC) due to human papillomavirus (HPV) infection has seen a dramatic increase in recent years. Bilateral tonsillar squamous cell carcinoma (biTSCC) has a much lower incidence than unilateral TSCC and three main hypotheses of biTSCC pathogenesis prevail: field carcinogenesis, single-clone, and multiple HPV infections.
A 49-year-old Male with a remote history of chewing tobacco presented with symptoms of spitting up tissue and occasional hemoptysis. Physical exam showed a sole left tonsillar mass which was confirmed to be TSCC on biopsy. The patient's computed tomographic (CT) scan was consistent with this finding; however, positron emission tomography (PET) scan indicated a second tumor in the contralateral right tonsil. Surgical resection of both masses and selective neck dissection was performed, and the specimens were sent for further pathological analysis. No complications of surgery were noted and the final diagnosis of synchronous biTSCC was made. The tumors were a T2N0M0 left poorly differentiated TSCC (p16+, EGFR+, bcl2+) with basaloid features, and a T1N0M0 right well to moderately differentiated TSCC (p16+, EGFR+, bcl2-).
Our present case was notable for differing tumor pathology and karyotype analysis between the right and left masses, directly supporting the multiple HPV infections hypothesis of biTSCC pathogenesis. Further genetic characterization of tonsillar tumors is needed to better characterize TSCC and best guide medical/surgical therapy.
近年来,由于人类乳头瘤病毒(HPV)感染,扁桃体鳞状细胞癌(TSCC)的发病率显著上升。双侧扁桃体鳞状细胞癌(biTSCC)的发病率远低于单侧 TSCC,目前主要有三种 biTSCC 发病机制的假说:场致癌、单克隆和多重 HPV 感染。
一名 49 岁男性,有咀嚼烟草的既往史,出现吐痰和偶尔咯血的症状。体格检查显示单一左扁桃体肿块,活检证实为 TSCC。患者的计算机断层扫描(CT)检查与此一致;然而,正电子发射断层扫描(PET)扫描表明右侧对侧扁桃体有第二个肿瘤。对两个肿块进行了手术切除和选择性颈部清扫术,并将标本送去进一步的病理分析。手术无并发症,最终诊断为同步双侧 TSCC。肿瘤为 T2N0M0 左侧低分化 TSCC(p16+,EGFR+,bcl2+),具有基底细胞样特征,以及 T1N0M0 右侧中至高度分化 TSCC(p16+,EGFR+,bcl2-)。
我们目前的病例值得注意的是,左右肿块的肿瘤病理学和核型分析不同,直接支持 biTSCC 发病机制的多重 HPV 感染假说。进一步对扁桃体肿瘤进行遗传特征分析,有助于更好地描述 TSCC 并指导最佳的医疗/手术治疗。