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

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...

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Autores principales: Wang, Jing, Xie, Liwu, Ma, Li, Miao, Yuchun, Guo, Jianghong, Xu, Enwei, Yang, Xuanqin, Su, Wen, Xi, Yanfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840991/
https://www.ncbi.nlm.nih.gov/pubmed/36654953
http://dx.doi.org/10.21037/gs-22-709
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author Wang, Jing
Xie, Liwu
Ma, Li
Miao, Yuchun
Guo, Jianghong
Xu, Enwei
Yang, Xuanqin
Su, Wen
Xi, Yanfeng
author_facet Wang, Jing
Xie, Liwu
Ma, Li
Miao, Yuchun
Guo, Jianghong
Xu, Enwei
Yang, Xuanqin
Su, Wen
Xi, Yanfeng
author_sort Wang, Jing
collection PubMed
description 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 ETV-6 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 ETV-6 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.
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spelling pubmed-98409912023-01-17 Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years Wang, Jing Xie, Liwu Ma, Li Miao, Yuchun Guo, Jianghong Xu, Enwei Yang, Xuanqin Su, Wen Xi, Yanfeng Gland Surg Case Report 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 ETV-6 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 ETV-6 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. AME Publishing Company 2022-12 /pmc/articles/PMC9840991/ /pubmed/36654953 http://dx.doi.org/10.21037/gs-22-709 Text en 2022 Gland Surgery. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Wang, Jing
Xie, Liwu
Ma, Li
Miao, Yuchun
Guo, Jianghong
Xu, Enwei
Yang, Xuanqin
Su, Wen
Xi, Yanfeng
Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title_full Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title_fullStr Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title_full_unstemmed Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title_short Two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
title_sort two cases report of secretory carcinoma of the salivary gland in the lung: one primary and one metastatic after many years
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840991/
https://www.ncbi.nlm.nih.gov/pubmed/36654953
http://dx.doi.org/10.21037/gs-22-709
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