涎腺内胸腺癌1例报告及文献复习。

Head and neck pathology Pub Date : 2022-09-01 Epub Date: 2021-11-22 DOI:10.1007/s12105-021-01394-6
Michał Kunc, Alexandra Kamieniecki, Grzegorz Walczak, Tomasz Nowicki, Bartosz Wasąg, Bogusław Mikaszewski, Dominik Stodulski, Wojciech Biernat
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引用次数: 4

摘要

异位胸腺癌很少在甲状腺中被诊断出来,更不用说甲状腺外组织了。在目前可用的文献中,只有5例甲状腺外恶性肿瘤与胸腺分化被报道为主要唾液腺。一位69岁的女性在左侧腮腺有一个缓慢生长的可触及的肿块。细针穿刺活检提示转移性癌,而核心穿刺活检提示高级别鳞状细胞癌。患者行左侧根治性腮腺切除术及选择性同侧淋巴结清扫及放疗。取手术标本进行组织病理学检查。显微镜下,肿瘤与胸腺癌相似。它由轮廓光滑的鳞状细胞组成的大巢,局部呈合胞生长模式,伴有丰富的淋巴细胞和反应性淋巴滤泡。外观类似胸腺小结节癌伴淋巴样增生。此外,肿瘤显示鳞状标记物(p40和p63)和胸腺癌标记物(CD5和CD117)的表达。因此,最终诊断为涎腺内胸腺癌。包括下一代测序在内的分子分析显示,没有变异具有强烈的、潜在的或未知的临床意义。随访1年,患者无疾病。在本病例中,我们全面介绍了腮腺cd5阳性鳞状细胞癌的临床、显微镜、分子和放射学图像。我们认为类似的病例应被指定为涎内胸腺癌,类似于类似的甲状腺肿瘤。我们的病例和有限的文献资料表明,由于其预后良好,应与传统的大唾液腺鳞状细胞癌区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intrasalivary Thymic Carcinoma: A Case Report and Literature Review.

Intrasalivary Thymic Carcinoma: A Case Report and Literature Review.

Intrasalivary Thymic Carcinoma: A Case Report and Literature Review.

Intrasalivary Thymic Carcinoma: A Case Report and Literature Review.

Ectopic thymic carcinomas are rarely diagnosed in the thyroid gland, let alone in extrathyroid tissues. In the currently available literature, only five cases of extrathyroidal malignancies with thymic differentiation have been reported as arising in the major salivary glands. A 69-year-old female presented with a slow-growing palpable mass in the left parotid gland. Fine needle aspiration biopsy suggested metastatic cancer, whereas core needle biopsy revealed high-grade squamous cell carcinoma. The patient underwent left radical parotidectomy with selective ipsilateral lymph node dissection and subsequent radiation therapy. The surgical specimen was taken for histopathological examination. Microscopically, the tumor resembled thymic carcinoma. It was composed of large nests of squamoid cells with smooth contours, focally with a syncytial growth pattern, and accompanied by abundant lymphocytes with reactive lymphoid follicles. This appearance resembled a micronodular thymic carcinoma with lymphoid hyperplasia. Moreover, the tumor displayed expression of squamous markers (p40 and p63) and markers of thymic carcinoma (CD5 and CD117). Therefore, the final diagnosis of intrasalivary thymic carcinoma was rendered. The molecular analysis including next-generation sequencing demonstrated no variants of the strong, potential, or unknown clinical significance. The patient remains disease-free at 1-year follow-up. In the current case, we comprehensively present a clinical, microscopic, molecular, and radiological picture of CD5-positive squamous cell carcinoma of the parotid. We postulate that similar cases should be designated as intrasalivary thymic carcinoma analogically to similar thyroid tumors. Our case and the limited literature data indicate they should be distinguished from conventional squamous cell carcinoma of major salivary glands due to their rather favorable prognosis.

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