Fibrosing mediastinitis (Q42995): Difference between revisions

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Mediastinite fibrosante, também conhecida como mediastinite esclerosante ou fibrose mediastínica é um transtorno caracterizado por uma reação fibrótica excessiva no mediastino. Pode resultar no comprometimento de vias aéreas, grandes vasos e outras estruturas mediastinais, com morbidade diretamente relacionada à localização e à extensão da fibrose. A causa mais comum é a histoplasmose, da qual é uma complicação rara e tardia, mas pode também ocorrem em associação com outras infecções e com transtornos autoimunes sistêmicos como a doença de Behçet, a granulomatose com poliangeíte e a fibrose retroperitoneal.
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Fibrosing mediastinitis, also known as sclerosing mediastinitis or mediastinal fibrosis, is a disorder characterised by an excessive fibrotic reaction in the mediastinum. It can result in compromise of airways, great vessels, and other mediastinal structures, with morbidity directly related to the location and extent of fibrosis. The commonest cause is histoplasmosis, of which it is a rare late complication, but it may also occur in association with other infections and with systemic autoimmune disorders such as Behçet disease, granulomatosis with polyangiitis and retroperitoneal fibrosis.

Revision as of 09:46, 13 August 2026

Fibrosing mediastinitis, also known as sclerosing mediastinitis or mediastinal fibrosis, is a disorder characterised by an excessive fibrotic reaction in the mediastinum. It can result in compromise of airways, great vessels, and other mediastinal structures, with morbidity directly related to the location and extent of fibrosis. The commonest cause is histoplasmosis, of which it is a rare late complication, but it may also occur in association with other infections and with systemic autoimmune disorders such as Behçet disease, granulomatosis with polyangiitis and retroperitoneal fibrosis.
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    Fibrosing mediastinitis
    Fibrosing mediastinitis, also known as sclerosing mediastinitis or mediastinal fibrosis, is a disorder characterised by an excessive fibrotic reaction in the mediastinum. It can result in compromise of airways, great vessels, and other mediastinal structures, with morbidity directly related to the location and extent of fibrosis. The commonest cause is histoplasmosis, of which it is a rare late complication, but it may also occur in association with other infections and with systemic autoimmune disorders such as Behçet disease, granulomatosis with polyangiitis and retroperitoneal fibrosis.

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