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两例肺内涎腺分泌性癌病例报告:一例为原发性,另一例为多年后的转移性。

Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years.

作者信息

Wang Jing, Xie Liwu, Ma Li, Miao Yuchun, Guo Jianghong, Xu Enwei, Yang Xuanqin, Su Wen, Xi Yanfeng

机构信息

Department of Pathology, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China.

Department of Hematology, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China.

出版信息

Gland Surg. 2022 Dec;11(12):2013-2020. doi: 10.21037/gs-22-709.

Abstract

BACKGROUND

Secretory carcinoma of the salivary gland (SCSG) is a recently discovered salivary gland tumor that occurs mostly in the major salivary glands and occasionally in the skin, cervix, trachea, etc. Secretory carcinoma of the lung is extremely rare. To our knowledge, this is the third report of SCSG arising as a primary pulmonary tumor. The two SCSG cases reported in this paper are unique in that one was primary and the other was metastasized to the lung.

CASE DESCRIPTION

Case 1 is a primary endobronchial tumor in a 66-year-old man. He went to the doctor complaining of fever, cough and yellow phlegm, and his body weight was significantly reduced by 3 kg. The bronchoscope showed the growth of new organisms in the right upper lobe of the lung. Immunohistochemistry of his biopsy specimen was positive for AE1/AE3, Keratin7 (CK7), S-100, mammaglobin, and pan-TRK, but negative for thyroid transcription factor-1 (TTF-1), napsin-A, synaptophysin (SYN), chromogranin A (CGA), and discovered on GIST-1 (Dog-1), and the MKI-67 (Ki-67) proliferation index was 2%. This case lacked the typical gene rearrangement. After one cycle of chemotherapy, the tumor was significantly reduced, and surgical excision was planned. Case 2 was a metastatic secretory carcinoma with a history of parotid pleomorphic adenoma resection 30 years ago and malignant pleomorphic adenoma resection 16 years ago before the study, respectively. He presented with a complaint of a parotid gland mass. Chest CT examination revealed a mass in the upper lobe of the left lung. The biopsy tissue of him exhibited a typical histological appearance under the microscope. Immunohistochemistry was positive for AE1/AE3, CK7, S-100, and mammaglobin; partially positive for estrogen receptor (ER) and pan-TRK; and negative for TTF-1, Napsin-A, SYN, CGA, P63, P40, and Dog-1. The Ki-67 proliferation index was approximately 3%. Fluorescence in situ hybridization (FISH) revealed gene rearrangement. After the diagnosis of SCSG, the patient underwent resection of the lung mass, and there was no recurrence of the lung after 1 month's follow-up.

CONCLUSIONS

By examining these two cases, we have a better understanding of the clinicopathological features of secretory carcinoma, which will help to improve the accuracy of pathological diagnosis.

摘要

背景

涎腺分泌性癌(SCSG)是一种最近发现的涎腺肿瘤,主要发生于大涎腺,偶尔也见于皮肤、宫颈、气管等部位。肺分泌性癌极为罕见。据我们所知,这是原发性肺分泌性癌的第三例报道。本文报道的两例SCSG病例具有独特性,其中一例为原发性,另一例为转移至肺部。

病例描述

病例1是一名66岁男性的原发性支气管内肿瘤。他因发热、咳嗽和咳黄痰就诊,体重明显减轻了3千克。支气管镜检查显示右肺上叶有新生物生长。其活检标本的免疫组化结果显示AE1/AE3、细胞角蛋白7(CK7)、S-100、乳腺珠蛋白和泛TRK呈阳性,但甲状腺转录因子-1(TTF-1)、 napsin-A、突触素(SYN)、嗜铬粒蛋白A(CGA)、GIST-1(Dog-1)呈阴性,且MKI-67(Ki-67)增殖指数为2%。该病例缺乏典型的基因重排。经过一个周期的化疗后,肿瘤明显缩小,计划进行手术切除。病例2是一例转移性分泌性癌,在研究前分别有30年前腮腺多形性腺瘤切除术和16年前恶性多形性腺瘤切除术的病史。他因腮腺肿块就诊。胸部CT检查显示左肺上叶有一肿块。其活检组织在显微镜下呈现典型的组织学表现。免疫组化结果显示AE1/AE3、CK7、S-100和乳腺珠蛋白呈阳性;雌激素受体(ER)和泛TRK部分阳性;TTF-1、Napsin-A、SYN、CGA、P63、P40和Dog-1呈阴性。Ki-67增殖指数约为3%。荧光原位杂交(FISH)显示有基因重排。在诊断为SCSG后,该患者接受了肺肿块切除术,随访1个月后肺部无复发。

结论

通过对这两例病例的研究,我们对分泌性癌的临床病理特征有了更好的了解,这将有助于提高病理诊断的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5d7/9840991/96cdca15be4c/gs-11-12-2013-f1.jpg

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