2020
DOI: 10.1016/j.rmcr.2019.100987
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Successful management of fibrosing mediastinitis with severe vascular compromise: Report of two cases and literature review

Abstract: Fibrosing mediastinitis is a rare disorder characterized by the invasive proliferation of fibrous tissue within the mediastinum. This fibrosis can result in compression of intrathoracic structures including the pulmonary vasculature leading to clinical symptoms and complications like pulmonary hypertension. Here, we present two cases of young patients with fibrosing mediastinitis complicated by pulmonary artery stenosis requiring medical and endovascular management with excellent results.

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Cited by 5 publications
(9 citation statements)
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“…1 , 3 , 8 FM may be an immune-mediated hypersensitivity to fungi or other antigens. 3 , 7 There are many known causes of FM. Granulomatous FM is associated with infections such as histoplasmosis, tuberculosis, blastomycosis, and cryptococcosis or with noninfectious diseases such as sarcoidosis.…”
Section: Discussionmentioning
confidence: 99%
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“…1 , 3 , 8 FM may be an immune-mediated hypersensitivity to fungi or other antigens. 3 , 7 There are many known causes of FM. Granulomatous FM is associated with infections such as histoplasmosis, tuberculosis, blastomycosis, and cryptococcosis or with noninfectious diseases such as sarcoidosis.…”
Section: Discussionmentioning
confidence: 99%
“…11 , 14 , 17 , 18 Statistically, 75% to 95% of the lesions are focal, while 5% to 25% are bilateral. 1 , 4 , 7 The severity of stenosis of the involved vessels can be noninvasively evaluated by echocardiography, CT angiography, or magnetic resonance imaging. Although magnetic resonance imaging is inferior to CT in terms of evaluating calcification, it can accurately identify invasive mediastinal soft tissue lesions in FM and invasion of adjacent structures.…”
Section: Discussionmentioning
confidence: 99%
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