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Calcifying fibrous tumor of the mediastinum: A case report
BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign mesenchymal tumor that often occurs in deep soft tissue of children and young adults. CFT rarely occurs in the mediastinum. CASE SUMMARY: In this paper, we describe a 31-year-old male patient with CFT in the mediastinum. The patient did not...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745323/ https://www.ncbi.nlm.nih.gov/pubmed/31559304 http://dx.doi.org/10.12998/wjcc.v7.i17.2637 |
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author | Qi, Dian-Jun Zhang, Qing-Fu |
author_facet | Qi, Dian-Jun Zhang, Qing-Fu |
author_sort | Qi, Dian-Jun |
collection | PubMed |
description | BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign mesenchymal tumor that often occurs in deep soft tissue of children and young adults. CFT rarely occurs in the mediastinum. CASE SUMMARY: In this paper, we describe a 31-year-old male patient with CFT in the mediastinum. The patient did not have any symptoms, and the posterior mediastinal lesion was unintentionally found during routine re-examination of thyroid cancer. The tumor had no adhesion to the surrounding tissue and was successfully and completely removed. Pathology showed a large amount of collagen-rich fibrous connective tissue. There was scattered dystrophic calcification and gravel in the fibrous tissue and a small amount of lymphocyte and plasma cell infiltration and lymphoid follicle formation in the interstitial fluid. In addition, findings showed 20 IgG4+ plasma cells per high-powered field of the diseased tissue, an IgG4+/IgG ratio of about 20%, and normal serum IgG4 levels. The final diagnosis was CFT of the mediastinum (CFTM). No evidence of tumor recurrence was observed by computed tomography at 3 mo after surgery. CONCLUSION: IgG4+ plasma cell enlargement may occur in CFTM, but clinical manifestations and serological tests suggest that it is not IgG4-related disease. We speculate that it may be an independent tumor subtype. |
format | Online Article Text |
id | pubmed-6745323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-67453232019-09-26 Calcifying fibrous tumor of the mediastinum: A case report Qi, Dian-Jun Zhang, Qing-Fu World J Clin Cases Case Report BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign mesenchymal tumor that often occurs in deep soft tissue of children and young adults. CFT rarely occurs in the mediastinum. CASE SUMMARY: In this paper, we describe a 31-year-old male patient with CFT in the mediastinum. The patient did not have any symptoms, and the posterior mediastinal lesion was unintentionally found during routine re-examination of thyroid cancer. The tumor had no adhesion to the surrounding tissue and was successfully and completely removed. Pathology showed a large amount of collagen-rich fibrous connective tissue. There was scattered dystrophic calcification and gravel in the fibrous tissue and a small amount of lymphocyte and plasma cell infiltration and lymphoid follicle formation in the interstitial fluid. In addition, findings showed 20 IgG4+ plasma cells per high-powered field of the diseased tissue, an IgG4+/IgG ratio of about 20%, and normal serum IgG4 levels. The final diagnosis was CFT of the mediastinum (CFTM). No evidence of tumor recurrence was observed by computed tomography at 3 mo after surgery. CONCLUSION: IgG4+ plasma cell enlargement may occur in CFTM, but clinical manifestations and serological tests suggest that it is not IgG4-related disease. We speculate that it may be an independent tumor subtype. Baishideng Publishing Group Inc 2019-09-06 2019-09-06 /pmc/articles/PMC6745323/ /pubmed/31559304 http://dx.doi.org/10.12998/wjcc.v7.i17.2637 Text en ©The Author(s) 2019. 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 Qi, Dian-Jun Zhang, Qing-Fu Calcifying fibrous tumor of the mediastinum: A case report |
title | Calcifying fibrous tumor of the mediastinum: A case report |
title_full | Calcifying fibrous tumor of the mediastinum: A case report |
title_fullStr | Calcifying fibrous tumor of the mediastinum: A case report |
title_full_unstemmed | Calcifying fibrous tumor of the mediastinum: A case report |
title_short | Calcifying fibrous tumor of the mediastinum: A case report |
title_sort | calcifying fibrous tumor of the mediastinum: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745323/ https://www.ncbi.nlm.nih.gov/pubmed/31559304 http://dx.doi.org/10.12998/wjcc.v7.i17.2637 |
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