Primary salivary gland squamous cell carcinoma with sialolithiasis in the submandibular gland: A case report and literature review

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Oral and Maxillofacial Surgery Medicine and Pathology Pub Date : 2024-01-09 DOI:10.1016/j.ajoms.2024.01.004
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引用次数: 0

Abstract

Primary salivary gland squamous cell carcinoma (SCC) is a very rare malignancy, and such a tumor with sialolithiasis is even rarer. Here, we report a case of 68-year-old man with primary salivary SCC and sialolithiasis. A cystic lesion with a salivary stone was found in the submandibular gland, lined by atypical epithelium with focal invasive focus. The atypical epithelium was positive for cytokeratin 5/6 and p40, and focally positive for p63, cytokeratin 14 and periodic acid-Schiff (PAS) stain. S-100 protein, calponin, α-smooth muscle actin, SOX10 and androgen receptor were negative and no mucin-containing cells were found on PAS with diastase and Alcian blue staining. The Ki-67 labeling index was relatively high. P53 was mostly negative, and no pathogenic TP53 mutations were detected. The diagnosis of primary salivary gland SCC was made. In our review including the present case, the speculated cause of primary salivary gland SCC was squamous metaplasia and dysplasia due to chronic irritation by a salivary stone. Although no cases with recurrence or distant metastasis were identified, more cases and long-term follow-up are needed.

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颌下腺原发性唾液腺鳞状细胞癌合并涎石症:病例报告和文献综述
原发性唾液腺鳞状细胞癌(SCC)是一种非常罕见的恶性肿瘤,而这种肿瘤同时伴有霰粒肿的情况则更为罕见。在此,我们报告了一例 68 岁男性原发性唾液腺鳞状细胞癌和涎石症患者的病例。在颌下腺发现了一个带有涎石的囊性病变,内衬为非典型上皮,有局灶性浸润灶。非典型上皮细胞角蛋白5/6和p40呈阳性,p63、细胞角蛋白14和周期性酸-Schiff(PAS)染色呈局部阳性。S-100蛋白、钙蛋白、α-平滑肌肌动蛋白、SOX10和雄激素受体均为阴性,在PAS与舒张酶和阿尔新蓝染色中未发现含粘蛋白的细胞。Ki-67 标记指数相对较高。P53大多为阴性,未发现致病性TP53突变。诊断结果为原发性唾液腺 SCC。在包括本病例在内的我们的研究中,原发性涎腺 SCC 的推测病因是涎石长期刺激导致的鳞状化生和发育不良。虽然没有发现复发或远处转移的病例,但仍需对更多病例进行长期随访。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
129
审稿时长
83 days
期刊最新文献
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