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Pulmonary sclerosing pneumocytoma, a rare tumor of the lung
Pulmonary sclerosing pneumocytoma (PSP) is a rare benign pulmonary tumor. Usually diagnosed incidentally by chest X-ray or chest CT scan. We presented a case of PSP in a 50-year-old woman who was diagnosed with a nodular lesion in the right lung. Thoracotomy was used for the excision of the mass. Pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389774/ https://www.ncbi.nlm.nih.gov/pubmed/30847275 http://dx.doi.org/10.1016/j.rmcr.2019.02.002 |
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author | Yalcin, Burcu Bekci, Taha Tahir Kozacioglu, Sumeyye Bolukbas, Ozden |
author_facet | Yalcin, Burcu Bekci, Taha Tahir Kozacioglu, Sumeyye Bolukbas, Ozden |
author_sort | Yalcin, Burcu |
collection | PubMed |
description | Pulmonary sclerosing pneumocytoma (PSP) is a rare benign pulmonary tumor. Usually diagnosed incidentally by chest X-ray or chest CT scan. We presented a case of PSP in a 50-year-old woman who was diagnosed with a nodular lesion in the right lung. Thoracotomy was used for the excision of the mass. Pathologic examination revealed no malignant cells. Immunohistochemical studies were performed. TTF-1 was (+), Napsin-A was found to be weakly (+). After surgical resection, the patient was followed up. |
format | Online Article Text |
id | pubmed-6389774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63897742019-03-07 Pulmonary sclerosing pneumocytoma, a rare tumor of the lung Yalcin, Burcu Bekci, Taha Tahir Kozacioglu, Sumeyye Bolukbas, Ozden Respir Med Case Rep Case Report Pulmonary sclerosing pneumocytoma (PSP) is a rare benign pulmonary tumor. Usually diagnosed incidentally by chest X-ray or chest CT scan. We presented a case of PSP in a 50-year-old woman who was diagnosed with a nodular lesion in the right lung. Thoracotomy was used for the excision of the mass. Pathologic examination revealed no malignant cells. Immunohistochemical studies were performed. TTF-1 was (+), Napsin-A was found to be weakly (+). After surgical resection, the patient was followed up. Elsevier 2019-02-13 /pmc/articles/PMC6389774/ /pubmed/30847275 http://dx.doi.org/10.1016/j.rmcr.2019.02.002 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Yalcin, Burcu Bekci, Taha Tahir Kozacioglu, Sumeyye Bolukbas, Ozden Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title | Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title_full | Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title_fullStr | Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title_full_unstemmed | Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title_short | Pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
title_sort | pulmonary sclerosing pneumocytoma, a rare tumor of the lung |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389774/ https://www.ncbi.nlm.nih.gov/pubmed/30847275 http://dx.doi.org/10.1016/j.rmcr.2019.02.002 |
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