Interstitial lung diseases (ILDs) or diffuse parenchymal (DPLDs) are a group of that is distinguished by subacute chronic inflammation and/or fibrosis. Family history currently being considered one the biggest risk factors for ILD. Rheumatoid arthritis (RA) systemic autoimmune disease has lungs as its most common extraarticular organ involved. associated with it major causes mortality along sev...

Background Antisynthetase syndrome (ASSD) is an autoimmune disease characterized by the presence of antiaminoacyl tRNA-synthetase antibodies (ARS) and clinical manifestations that may include interstitial lung (ILD), myositis, arthritis, Raynaud´s phenomenon (RP), fever mechanic’s hands (MHs). The incidence rate unknown no population epidemiological studies have been published. Objectives To de...

 ABSTRACT Background: Cholesterol cleft granulomas with clusters of giant cells were noted to be a common feature of non-specific interstitial pneumonia (NSIP). Objective: This study aimed to define the cell populations involved in the granulomas. Methods: The granulomas of 16 patients with cryptogenic fibrosing alveolitis (five cases with the histological features ofNSIP, five with those ofUIP...

TOPIC: Diffuse Lung Disease TYPE: Medical Student/Resident Case Reports INTRODUCTION: Anti-synthetase syndrome is an idiopathic inflammatory myopathy caused by autoantibody production against aminoacyl transfer RNA synthetases (anti-RSA antibodies). There are currently nine RSA antibodies: Jo1, OJ, EJ, KS, Wa, YR, Zo, PL-7, and PL-12. This associated with interstitial lung disease (ILD), polyar...

Introduction. The possible formation of persistent residual changes in the lung after a COVID-19 began to be reported first wave pandemic, but their extent and prevalence have not been fully assessed. Purpose study. Evaluate CT patterns lesions. Materials methods. We analyzed clinical radiation data 868 patients (f/m — 441/427) who underwent were observed clinics First St.-Petersburg State Medi...

The study examines whether clinical and objective improvement can be achieved in patients with LBP (low back pain) radicular symptoms using a 6-week exercise program based on press up exercises created from ADL (activities of daily living) movement patterns. This original involved 10 men acute L5 / S1 disc hernia. Before starting the program, determined intensity pain VAS (Visual Analogue Scale...

Background Progressive pulmonary fibrosis (PPF) is characterized by deterioration of respiratory symptoms, lung function decline and progressive on high-resolution computed tomography (HRCT). It associated with poor prognosis. Patients connective tissue disease-related interstitial disease (CTD-ILD) may also develop PPF need intensified clinical management. However, different criteria for are u...

Background Since publication of clinical trials regarding the efficacy nintedanib in fibrosing ILD, including ILD associated with autoimmune diseases, its use has increased but not enough real-world data been published. Objectives The aim our study was to evaluate and safety patients interstitial lung diseases (ILDs) progressively several etiologies a spanish third-level hospital. Methods A ret...

Background Idiopathic inflammatory myopathies (IIM) are a group of heterogeneous autoimmune disorders marked by skeletal muscle inflammation and extra-muscular complications including pulmonary involvement. Interstitial lung disease (ILD) is common manifestation affecting up to 78% in IIM patients. Methods means for in-vivo visualization ongoing tissue remodeling affected organs scarce. Objecti...

Background The Idiopathic Inflammatory Myositis (IIM) are heterogeneous with different clinical profiles associated various myositis autoantibodies. Among the specific antibodies (MSA), against aminoacyl-tRNA synthetases(ARS) is related to clinically unique IIM subsets, Antisynthetase syndrome(ASS). Objectives aim of this study was identify prevalence and features patients ARS autoantibodies co...