Unclassifiable interstitial lung disease

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Prevalence and prognosis of unclassifiable interstitial lung disease.

The aim of this study was to determine the prevalence, characteristics and outcomes of patients with unclassifiable interstitial lung disease (ILD) and to develop a simple method of predicting disease behaviour. Unclassifiable ILD patients were identified from an ongoing longitudinal cohort. Unclassifiable ILD was diagnosed after a multidisciplinary review did not secure a specific ILD diagnosi...

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Prevalence and prognosis of unclassifiable interstitial lung disease

The aim of this study was to determine the prevalence, characteristics and outcomes of patients with unclassifiable interstitial lung disease (ILD) and to develop a simple method of predicting disease behaviour. Unclassifiable ILD patients were identified from an ongoing longitudinal cohort. Unclassifiable ILD was diagnosed after a multidisciplinary review did not secure a specific ILD diagnosi...

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Unclassifiable interstitial lung disease: an unresolved diagnostic dilemma

Interstitial lung disease (ILD) classification requires a multidisciplinary review that includes input from an ILD clinician, chest radiologist, and lung pathologist. We report a case of ILD that remained unclassifiable due to discordant clinical, radiological, and pathological findings despite a thorough evaluation that included examination of explanted lung tissue. This case demonstrates that...

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Unclassified or unclassifiable interstitial lung disease: confusing or helpful disease category?

Since the seminal report by Averill A. Liebow in 1968 [1] of the first classification of idiopathic interstitial pneumonias (IIPs), consisting of five entities including ‘‘usual or classical interstitial pneumonia’’ (UIP), a secure diagnosis has, until recently, required histopathological evaluation. A histologically based classification might appear paradoxical, as a biopsy is performed in onl...

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Inherited interstitial lung disease.

This article focuses on recent advances in the identification of genes and genetic polymorphisms that have been implicated in the development of human interstitial lung diseases. It focuses on the inherited mendelian diseases in which pulmonary fibrosis is part of the clinical phenotype and the genetics of familial idiopathic pulmonary fibrosis and other rare inherited interstitial lung disease...

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ژورنال

عنوان ژورنال: Current Opinion in Pulmonary Medicine

سال: 2018

ISSN: 1070-5287

DOI: 10.1097/mcp.0000000000000509