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Fibrosing mediastinitis: when to suspect and how to evaluate?

Fibrosing mediastinitis (FM), which is also known as mediastinal fibrosis or sclerosing mediastinitis, is an uncommon, benign and progressive condition characterized by an invasive proliferation of fibrous tissue within the mediastinum. Tuberculosis and histoplasmosis are the major causes of the gra...

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Autores principales: Jain, Neeraj, Chauhan, Udit, Puri, Sunil Kumar, Agrawal, Sachin, Garg, Lalit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195926/
https://www.ncbi.nlm.nih.gov/pubmed/30364448
http://dx.doi.org/10.1259/bjrcr.20150274
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author Jain, Neeraj
Chauhan, Udit
Puri, Sunil Kumar
Agrawal, Sachin
Garg, Lalit
author_facet Jain, Neeraj
Chauhan, Udit
Puri, Sunil Kumar
Agrawal, Sachin
Garg, Lalit
author_sort Jain, Neeraj
collection PubMed
description Fibrosing mediastinitis (FM), which is also known as mediastinal fibrosis or sclerosing mediastinitis, is an uncommon, benign and progressive condition characterized by an invasive proliferation of fibrous tissue within the mediastinum. Tuberculosis and histoplasmosis are the major causes of the granulomatous variety, while non-granulomatous FM is an idiopathic reaction to autoimmune syndromes, drugs and radiation. Contrast-enhanced CT is the investigation of choice that can diagnose, and assess the extent and the severity of involvement. We are presenting a case of FM in a young female who presented with complaints of breathlessness, occasional cough and diffuse chest pain for 3 months.
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spelling pubmed-61959262018-10-25 Fibrosing mediastinitis: when to suspect and how to evaluate? Jain, Neeraj Chauhan, Udit Puri, Sunil Kumar Agrawal, Sachin Garg, Lalit BJR Case Rep Case Report Fibrosing mediastinitis (FM), which is also known as mediastinal fibrosis or sclerosing mediastinitis, is an uncommon, benign and progressive condition characterized by an invasive proliferation of fibrous tissue within the mediastinum. Tuberculosis and histoplasmosis are the major causes of the granulomatous variety, while non-granulomatous FM is an idiopathic reaction to autoimmune syndromes, drugs and radiation. Contrast-enhanced CT is the investigation of choice that can diagnose, and assess the extent and the severity of involvement. We are presenting a case of FM in a young female who presented with complaints of breathlessness, occasional cough and diffuse chest pain for 3 months. The British Institute of Radiology 2016-01-19 /pmc/articles/PMC6195926/ /pubmed/30364448 http://dx.doi.org/10.1259/bjrcr.20150274 Text en © 2016 The Authors. Published by the British Institute of Radiology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Jain, Neeraj
Chauhan, Udit
Puri, Sunil Kumar
Agrawal, Sachin
Garg, Lalit
Fibrosing mediastinitis: when to suspect and how to evaluate?
title Fibrosing mediastinitis: when to suspect and how to evaluate?
title_full Fibrosing mediastinitis: when to suspect and how to evaluate?
title_fullStr Fibrosing mediastinitis: when to suspect and how to evaluate?
title_full_unstemmed Fibrosing mediastinitis: when to suspect and how to evaluate?
title_short Fibrosing mediastinitis: when to suspect and how to evaluate?
title_sort fibrosing mediastinitis: when to suspect and how to evaluate?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195926/
https://www.ncbi.nlm.nih.gov/pubmed/30364448
http://dx.doi.org/10.1259/bjrcr.20150274
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