Primary squamous cell carcinoma of the parotid salivary gland: a clinical observation

N. A. Ognerubov, A. O. Khizhnyak, М. A. Ognerubova, R. S. Sergeev, L. V. Polyakova
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Abstract

Introduction. Malignant tumors of the salivary glands account for 3–5 % of all cases of head and neck cancer. Squamous cell carcinoma is the rarest histological variant of this pathology. It accounts for an average of 1.6 %. Among large salivary gland tumors, squamous cell carcinoma most often occurs in the parotid salivary gland.Aim. To present a clinical case of primary disseminated cancer of the parotid salivary gland with squamous cell structure.Clinical observation. A 70-year-old patient was under observation who was diagnosed with a primary squamous cell tumor of the parotid salivary gland with multiple metastases during a complex examination. He was sick for about 6 months when asymmetry of left half of the face appeared due to a painful neoplasm in the parotid salivary gland. Recently, the patient has noted increased tumor growth. Objective examination revealed peripheral paralysis of the facial nerve on the left. In the parotid-masticatory region on the left, with a transition to the zygomatic region, there is a dense painful immobile exophytic tumor with infiltration into soft tissues of the face and skin 6.5 × 5.0 cm in size with an ulcer in the center. Laterally, it reaches the tragus, and at the bottom-the angle of the lower jaw. In the submandibular region on the left, metastatic lymph nodes 2.5 × 2.0 cm in size are palpated. A biopsy was collected. Histological conclusion: non-keratinizing squamous cell carcinoma. Expression of the programmed death receptor ligand (PD-L1) in the tumor is negative. Mutations of genes Her2-neu and BRAF were not detected. According to medical imaging methods, multiple metastases were found in the lungs, liver, zygomatic bone and tumor growth in the maxillary sinus on the left. The diagnosis was established: cancer of the parotid salivary gland, stage IVC, cT4N1M1, with metastases to the liver, lungs and bones. Polychemotherapy was prescribed according to the scheme: 5-fluorouracil + cisplatin + cetuximab + bisphosphonates. After 3 cycles, a partial regression is obtained.Conclusion. The primary squamous cell carcinoma is prone to an aggressive course and has an unfavorable prognosis, especially in patients over 60 years of age with skin and facial nerve damage, as well as the presence of regional and distant metastases. Differential diagnosis is necessary to exclude the secondary nature of the tumor. The presented case is a rare example of primary squamous cell carcinoma of the parotid salivary gland with extensive metastatic lesion and regression of the pathological process after polychemotherapy in combination with targeted therapy.
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腮腺唾液腺原发性鳞状细胞癌:临床观察
导言。唾液腺恶性肿瘤占头颈部癌症病例总数的 3-5%。鳞状细胞癌是这种病理组织学变异中最罕见的一种。平均占 1.6%。在大型唾液腺肿瘤中,鳞状细胞癌最常发生在腮腺唾液腺。介绍一例腮腺鳞状细胞结构原发性播散性癌的临床病例。观察对象是一名 70 岁的患者,在一次复杂的检查中被诊断为腮腺唾液腺原发性鳞状细胞肿瘤并伴有多处转移。他患病约 6 个月,由于腮腺唾液腺肿瘤疼痛,左半边脸出现不对称。最近,患者发现肿瘤增大。客观检查发现左侧面神经周围麻痹。在左侧腮腺-咀嚼区,向颧骨区过渡处,有一个致密的、不移动的外生肿瘤,疼痛剧烈,浸润到面部软组织和皮肤,大小为 6.5 × 5.0 厘米,中心有溃疡。肿瘤侧面到达外耳道,底部到达下颌角。在左侧的颌下区,可触及 2.5 × 2.0 厘米大小的转移性淋巴结。进行了活检。组织学结论:非角化性鳞状细胞癌。肿瘤中程序性死亡受体配体(PD-L1)的表达为阴性。未检测到 Her2-neu 和 BRAF 基因突变。根据医学影像方法,发现肺部、肝脏、颧骨有多处转移,左侧上颌窦有肿瘤生长。诊断确定:腮腺唾液腺癌,IVC 期,cT4N1M1,肝、肺、骨转移。多化疗方案为:5-氟尿嘧啶+顺铂+西妥昔单抗+双膦酸盐。3 个周期后,患者的病情得到了部分缓解。原发性鳞状细胞癌的病程较长,预后较差,尤其是对于 60 岁以上、有皮肤和面部神经损伤以及区域和远处转移的患者。必须进行鉴别诊断,以排除肿瘤的继发性。本病例是一例罕见的腮腺唾液腺原发性鳞状细胞癌,伴有广泛转移病灶,经多化疗联合靶向治疗后病理过程消退。
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