Fibrotic hypersensitivity pneumonitis (fHP) is a frequently misdiagnosed fibrosing interstitial pneumonia, which often remains undiagnosed due to the lack of uniformity of diagnostic criteria. Its features are similar to those of other ILDs, especially idiopathic pulmonary fibrosis (IPF), and biomarkers with potential clinical value have been proposed.
D'Alessandro, M., Bergantini, L., Cameli, P., Landi, C., Lanzarone, N., Perrone, A., et al. (2022). Peripheral and alveolar biomarkers of fibrotic hypersensitivity pneumonitis. PANMINERVA MEDICA, 64(4), 548-554 [10.23736/S0031-0808.20.04056-2].
Peripheral and alveolar biomarkers of fibrotic hypersensitivity pneumonitis
D'Alessandro, Miriana;Bergantini, Laura;Cameli, Paolo;Lanzarone, Nicola;Perillo, Felice;Bianchi, Francesco;Refini, Rosa M;Pieroni, Maria;Sestini, Piersante;Bargagli, Elena
2022-01-01
Abstract
Fibrotic hypersensitivity pneumonitis (fHP) is a frequently misdiagnosed fibrosing interstitial pneumonia, which often remains undiagnosed due to the lack of uniformity of diagnostic criteria. Its features are similar to those of other ILDs, especially idiopathic pulmonary fibrosis (IPF), and biomarkers with potential clinical value have been proposed.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
Utilizza questo identificativo per citare o creare un link a questo documento:
https://hdl.handle.net/11365/1122082