Interstitial pneumonia with autoimmune feature (IPAF) is a recently established disease entity that is comprised of interstitial lung diseases with evidence of autoimmune features but that does not fulfill the criteria for definite autoimmune rheumatic diseases. The classification criteria for IPAF were defined by the European Respiratory Society and American Thoracic Society in 2015. However, further studies to establish IPAF subgroups and treatment modalities for each subgroup are still needed. In this review, we discuss recent advances regarding IPAF and raise critical points for the diagnosis and management of patients with IPAF from the perspective of rheumatologists
The diagnosis of interstitial lung disease (ILD) requires meticulous evaluation for an underlying co...
Background: Interstitial lung diseases (ILDs) are a heterogeneous group of disorders characterized b...
Interstitial pneumonia with autoimmune features (IPAF) is a term to describe individuals with both i...
International audienceThe presence of clinical, serological and/or radiological features suggestive,...
The term interstitial pneumonia with autoimmune features (IPAF) has been proposed to define patients...
A significant proportion of patients with interstitial lung disease (ILD) manifest autoimmune featur...
Objective The classification interstitial pneumonia with autoimmune features (IPAF) includes patient...
BACKGROUND: Interstitial pneumonia with autoimmune features (IPAF) has recently been defined by an i...
Background and objective: Recently the term “interstitial pneumonia with autoimmune features” (IPAF)...
IPAF classification criteria include several autoimmune conditions with different evolution. The pr...
Patients with interstitial lung disease (ILD) may have features of connective tissue disease (CTD), ...
Abstract Background Interstitial pneumonia with autoimmune features (IPAF) identifies a recently rec...
In 2015 the European Respiratory Society (ERS) and the American Thoracic Society (ATS) “Task Force o...
To evaluate the rate of progression towards specific autoimmune diseases (SADs) of a prospective, mu...
The opportunity of a multidisciplinary evaluation for the diagnosis of interstitial pneumonias highl...
The diagnosis of interstitial lung disease (ILD) requires meticulous evaluation for an underlying co...
Background: Interstitial lung diseases (ILDs) are a heterogeneous group of disorders characterized b...
Interstitial pneumonia with autoimmune features (IPAF) is a term to describe individuals with both i...
International audienceThe presence of clinical, serological and/or radiological features suggestive,...
The term interstitial pneumonia with autoimmune features (IPAF) has been proposed to define patients...
A significant proportion of patients with interstitial lung disease (ILD) manifest autoimmune featur...
Objective The classification interstitial pneumonia with autoimmune features (IPAF) includes patient...
BACKGROUND: Interstitial pneumonia with autoimmune features (IPAF) has recently been defined by an i...
Background and objective: Recently the term “interstitial pneumonia with autoimmune features” (IPAF)...
IPAF classification criteria include several autoimmune conditions with different evolution. The pr...
Patients with interstitial lung disease (ILD) may have features of connective tissue disease (CTD), ...
Abstract Background Interstitial pneumonia with autoimmune features (IPAF) identifies a recently rec...
In 2015 the European Respiratory Society (ERS) and the American Thoracic Society (ATS) “Task Force o...
To evaluate the rate of progression towards specific autoimmune diseases (SADs) of a prospective, mu...
The opportunity of a multidisciplinary evaluation for the diagnosis of interstitial pneumonias highl...
The diagnosis of interstitial lung disease (ILD) requires meticulous evaluation for an underlying co...
Background: Interstitial lung diseases (ILDs) are a heterogeneous group of disorders characterized b...
Interstitial pneumonia with autoimmune features (IPAF) is a term to describe individuals with both i...