Abstract |
Fibrosing mediastinitis (FM), also called sclerosing mediastinitis or mediastinal fibrosis, is a rare disease characterized by excessive fibrotic reaction in the mediastinum and may compromise the airway, the great vessels and other mediastinal structures, with a morbidity directly related to the location and extent of fibrosis. The cause is not always known but is often the result of a granulomatous disease, most often the histoplasmosis. We report a 43-year-old woman with a history of tuberculosis infection 23 years ago. She attended the pulmonology clinic for cough and dyspnea. Physical examination revealed jugular venous distention at 90°. In computed tomography scan of the chest with contrast (c/c), we observed a mediastinal nodal cast provoking cava compression and obliteration of main and intermediary right lobar bronchus. The pathological examination was FM.
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Authors | Marta Ferrer Galván, José Antonio Rodríguez Portal, María Pilar Serrano Gorarredona, Lourdes Gómez Izquierdo |
Journal | The clinical respiratory journal
(Clin Respir J)
Vol. 9
Issue 1
Pg. 125-8
(Jan 2015)
ISSN: 1752-699X [Electronic] England |
PMID | 24405501
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2014 John Wiley & Sons Ltd. |
Topics |
- Adult
- Diagnosis, Differential
- Female
- Humans
- Mediastinitis
(complications, diagnosis, therapy)
- Sarcoidosis
(diagnosis)
- Sclerosis
(complications, diagnosis, therapy)
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