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Lung in idiopathic inflammatory myopathies (CROSBI ID 47100)

Prilog u knjizi | ostalo

Peroš-Golubičić, Tatjana: Samaržija, Miroslav Lung in idiopathic inflammatory myopathies // Lung in non-pulmonary and systemic disease / Peroš-Golubičić, Tatjana (ur.). Zagreb: Medicinska naklada, 2013. str. 299-312

Podaci o odgovornosti

Peroš-Golubičić, Tatjana: Samaržija, Miroslav

engleski

Lung in idiopathic inflammatory myopathies

Lung involvement is frequent in patients with idiopathic inflammatory myopathies. The most common manifestations are diverse parenchymal diseases, interstitial lung diseases, infections, and hypoventilation respiratory failure due to weakness of respiratory muscle. The clinical picture may be acute in need of treatment in intensive care unit, or it can show slow progressive course. Therapy of ILD in patients with IIM is of utmost importance for their outcome and the survival. There are no controlled studies because myositis is a rare disease, and pulmonary interstitial manifestations even rarer. The corticosteroid and other immunosuppressive agents, methotrexate, cyclophosphamide and azathiprine are used with sufficient efficacy in most cases.

Inflammatory myopathies, pulmonary manifestations

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Podaci o prilogu

299-312.

objavljeno

Podaci o knjizi

Lung in non-pulmonary and systemic disease

Peroš-Golubičić, Tatjana

Zagreb: Medicinska naklada

2013.

978-953-176-577-0

Povezanost rada

Kliničke medicinske znanosti