2023
DOI: 10.1016/j.ccm.2023.06.003
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Interstitial Lung Disease and Sarcoidosis

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Cited by 5 publications
(2 citation statements)
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“…Interstitial lung diseases (ILDs) are defined as a heterogeneous group of idiopathic or secondary conditions that share a similar clinical, radiological, and histologic pattern characterized by inflammation and fibrosis involving the lung interstitium [1]. Overall, the prevalence of ILDs is approximately 200 individuals per 100,000 [2]. An early and accurate differential diagnosis among undetermined ILDs is usually pivotal to predicting prognosis and determining the best pharmacological therapy.…”
Section: Introductionmentioning
confidence: 99%
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“…Interstitial lung diseases (ILDs) are defined as a heterogeneous group of idiopathic or secondary conditions that share a similar clinical, radiological, and histologic pattern characterized by inflammation and fibrosis involving the lung interstitium [1]. Overall, the prevalence of ILDs is approximately 200 individuals per 100,000 [2]. An early and accurate differential diagnosis among undetermined ILDs is usually pivotal to predicting prognosis and determining the best pharmacological therapy.…”
Section: Introductionmentioning
confidence: 99%
“…An early and accurate differential diagnosis among undetermined ILDs is usually pivotal to predicting prognosis and determining the best pharmacological therapy. International consensus guidelines recommend the need for a precise histopathological diagnosis in undetermined ILD patients in whom clinical, laboratory, and high-resolution computed tomography findings, preferably discussed within a multidisciplinary panel, prove insufficient to make a confident diagnosis [2,3]. In these instances, surgical lung biopsy is still the recommended diagnostic procedure despite the proposal of alternative techniques such as transbronchial lung cryobiopsy [4].…”
Section: Introductionmentioning
confidence: 99%