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Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report

BACKGROUND: Primary malignant melanoma of the lung (PMML) is a rare and highly malignant tumor with a poor prognosis. Here, we report a PMML case diagnosed by computed tomography (CT)-guided percutaneous biopsy, describe its pathological features and review relevant literature to improve our underst...

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Autores principales: Xi, Jian-Min, Wen, Huan, Yan, Xue-Bing, Huang, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760437/
https://www.ncbi.nlm.nih.gov/pubmed/33392320
http://dx.doi.org/10.12998/wjcc.v8.i24.6373
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author Xi, Jian-Min
Wen, Huan
Yan, Xue-Bing
Huang, Jin
author_facet Xi, Jian-Min
Wen, Huan
Yan, Xue-Bing
Huang, Jin
author_sort Xi, Jian-Min
collection PubMed
description BACKGROUND: Primary malignant melanoma of the lung (PMML) is a rare and highly malignant tumor with a poor prognosis. Here, we report a PMML case diagnosed by computed tomography (CT)-guided percutaneous biopsy, describe its pathological features and review relevant literature to improve our understanding of this tumor. CASE SUMMARY: A 64-year-old Chinese female presented with productive cough for 7 mo. A chest CT scan showed a large and space-occupying lesion in Lingual lobe. Positron emission tomography-CT revealed multiple nodules located in the superior lobe apicoposterior segment of her left lung. Brain magnetic resonance imaging showed numerous enhancing nodules, suggesting brain metastasis. Abdominal CT scan did not show any abnormalities. By CT-guided percutaneous biopsy, four pieces of gray and taupe tissues (1 cm length and 0.1 mm in diameter) were obtained. After pathologic examination, the tumor was found to consist of epidermal and nested small round cells, fibrosis and thin-walled blood vessels. The finding was suggestive of malignant melanoma. To confirm the diagnosis, pathological morphology and immunophenotypic features of the biopsy specimens were observed. The patient denied any history of skin tumors. No abnormal lesions were detected in other sites of the body. Molecular testing was positive for wild-type EGFR and KIT gene mutations. Finally, the clinical and pathological findings suggested PMML. CONCLUSION: PMML is very rare, and the percutaneous biopsy tissue is limited. Therefore, comprehensive consideration of histology, immunohistochemistry, imaging, and clinical information is important for the diagnosis of PMML.
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spelling pubmed-77604372021-01-01 Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report Xi, Jian-Min Wen, Huan Yan, Xue-Bing Huang, Jin World J Clin Cases Case Report BACKGROUND: Primary malignant melanoma of the lung (PMML) is a rare and highly malignant tumor with a poor prognosis. Here, we report a PMML case diagnosed by computed tomography (CT)-guided percutaneous biopsy, describe its pathological features and review relevant literature to improve our understanding of this tumor. CASE SUMMARY: A 64-year-old Chinese female presented with productive cough for 7 mo. A chest CT scan showed a large and space-occupying lesion in Lingual lobe. Positron emission tomography-CT revealed multiple nodules located in the superior lobe apicoposterior segment of her left lung. Brain magnetic resonance imaging showed numerous enhancing nodules, suggesting brain metastasis. Abdominal CT scan did not show any abnormalities. By CT-guided percutaneous biopsy, four pieces of gray and taupe tissues (1 cm length and 0.1 mm in diameter) were obtained. After pathologic examination, the tumor was found to consist of epidermal and nested small round cells, fibrosis and thin-walled blood vessels. The finding was suggestive of malignant melanoma. To confirm the diagnosis, pathological morphology and immunophenotypic features of the biopsy specimens were observed. The patient denied any history of skin tumors. No abnormal lesions were detected in other sites of the body. Molecular testing was positive for wild-type EGFR and KIT gene mutations. Finally, the clinical and pathological findings suggested PMML. CONCLUSION: PMML is very rare, and the percutaneous biopsy tissue is limited. Therefore, comprehensive consideration of histology, immunohistochemistry, imaging, and clinical information is important for the diagnosis of PMML. Baishideng Publishing Group Inc 2020-12-26 2020-12-26 /pmc/articles/PMC7760437/ /pubmed/33392320 http://dx.doi.org/10.12998/wjcc.v8.i24.6373 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Xi, Jian-Min
Wen, Huan
Yan, Xue-Bing
Huang, Jin
Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title_full Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title_fullStr Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title_full_unstemmed Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title_short Primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: A case report
title_sort primary pulmonary malignant melanoma diagnosed with percutaneous biopsy tissue: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760437/
https://www.ncbi.nlm.nih.gov/pubmed/33392320
http://dx.doi.org/10.12998/wjcc.v8.i24.6373
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