A5040267729- Autoimmune and Inflammatory Disorders Research
- Inflammasome and immune disorders
- Systemic Lupus Erythematosus Research
- Adolescent and Pediatric Healthcare
- Spondyloarthritis Studies and Treatments
- Rheumatoid Arthritis Research and Therapies
- Inflammatory Myopathies and Dermatomyositis
- Eosinophilic Esophagitis
- Immunodeficiency and Autoimmune Disorders
- Elbow and Forearm Trauma Treatment
- Renal Diseases and Glomerulopathies
- Orthopedic Infections and Treatments
- Liver Diseases and Immunity
- Child and Adolescent Health
- Dermatological and Skeletal Disorders
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Infectious Diseases and Tuberculosis
- Childhood Cancer Survivors' Quality of Life
- Osteomyelitis and Bone Disorders Research
- Systemic Sclerosis and Related Diseases
- Otitis Media and Relapsing Polychondritis
- Parvovirus B19 Infection Studies
- Scoliosis diagnosis and treatment
- Esophageal and GI Pathology
- Vasculitis and related conditions
Wojskowy Instytut Medyczny
2019-2025
National Institute of Geriatrics, Rheumatology and Rehabilitation
2013-2024
Wojskowy Instytut Medycyny Lotniczej
2023
Center for Rheumatology
2021
American College of Rheumatology
2014
Fundacion Instituto de Reumatologia Fernando Chalem
2013-2014
Institute of Rheumatology
2011
The full thickness resection is an innovative technique that enables non-exposed endoscopic full-thickness (EFTR) of superficial and subepithelial gastrointestinal lesions. This retrospective, multicenter study evaluated the effectiveness safety EFTR in gastroduodenal colorectal resections. Data from 105 consecutive procedures at 6 Polish centers were analyzed. Patients divided into three groups: 'difficult adenoma', adenocarcinoma, or lesion (SEL). Outcomes assessed R0 adverse event rates,...
Scleroderma is a rare, autoimmune, chronic condition that affects the connective tissue by excessive collagen production. If diagnosed before age of 16, it referred to as juvenile scleroderma. There are two major types condition: localized and generalized Localized scleroderma has much higher incidence than type which extremely rare among children mostly adults. In either case, imaging can prove be useful in both diagnosis monitoring disease. this article, we aim review findings present...
To evaluate the long-term safety and efficacy of etanercept treatment in Polish patients with juvenile idiopathic arthritis (JIA).The study involved patients, fulfilling JIA criteria International League Associations Rheumatology (ILAR), who were started on therapy after methotrexate other synthetic disease-modifying antirheumatic drugs (DMARDs) had proven ineffective. Patient data collected an electronic registry. Disease improvement was assessed based Giannini's criteria.The statistical...
Abstract Juvenile idiopathic arthritis is the most frequent rheumatic disease in pediatric population, followed by systemic lupus erythematosus, juvenile scleroderma syndromes, dermatomyositis, chronic recurrent multifocal osteomyelitis, and vasculopathies. The imaging approach to inflammatory connective tissue diseases childhood has not changed dramatically over last decade, with radiographs still leading method for bony pathology assessment, monitoring, evaluation of growth disturbances....
Secondary hemophagocytic lymphohistiocytosis (sHLH) is a life-threatening syndrome of severe hyperinflammation which often triggered by infection or autoimmune disease (macrophage activation - MAS). The aim our study was to assess the frequency sHLH/MAS in children treated institution and compare effectiveness various therapeutic interventions.Between 2005 2013, 24 (age: 1-17 years) were consecutively for sHLH/MAS. Therapy based on glucocorticoids (GCs) high standard doses (hd-GCs sd-GCs),...
Background: Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease among children. In some patients, cervical spine remains a serious and chronic manifestation of JIA. The aim this study was to assess frequency lesions on radiographs MRI in JIA patients with clinical signs involvement verify if addition MRI, use could be abandoned. Methods: This retrospective evaluated consecutive 34 children (25 girls; aged 6–18 years, median 15.5 years) spine. each patient, both were...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid metabolism caused by deficiency the lysosomal enzyme α-galactosidase A. Progressive deposition GL-3 starts early in life, presumably as fetal life. Chronic burning or provoked attacks excruciating pain hands and feet are common most children well GI-symptoms.We describe case pediatric with gastrointestinal dysmotility symptoms primary severe complaints. Colonic pseudoobstruction necrosis developed age 15 years. We...
The authors present a very rare case of juvenile spondyloarthritis and chronic recurrent multifocal osteomyelitis overlap syndrome in 16-year-old girl discuss diagnostic difficulties associated with this case.Juvenile spondyloarthropathies are type rheumatic diseases characterized by non-symmetrical peripheral arthritis enthesitis as well spondylitis.Chronic is rare, possibly autoimmune disease found primarily children adolescents.The bone marrow inflammation the presence lytic sclerotic...
Objectives Mixed connective tissue disease is a rare systemic of developmental age and it includes the features arthritis, polymyositis/dermatomyositis, lupus erythematosus sclerosis, with presence anti-ribonucleoprotein antibodies (anti-RNP) in serum. Early diagnosis difficult but essential preventing development complications, which are often irreversible. International literature does not report many studies on large cohorts children this disease. The aim retrospective study was to define...
This retrospective case-control study aimed to evaluate whether Magnetic Resonance Imaging (MRI) enables differentiation of ankle arthritis in Juvenile Idiopathic Afrthritis JIA from arthralgia unknown aetiology patients clinically suspected JIA. Forty-four children, at ages 5-16, who underwent MRI the January 2016 March 2021 for active course were included. findings both groups-patients with final diagnosis and without JIA-were compared scored. The sum scores 22 lesions an individual...
The systemic form of scleroderma (SSc) in children is a very rare disease; therefore, it recognized relatively late, which increases the risk complications. aim study was to assess clinical symptoms juvenile sclerosis (JSSc) our cohort patients.
Chronic non-bacterial osteomyelitis (CNO) is a rare autoinflammatory bone disease, affecting mainly children. CNO includes broad clinical spectrum of symptoms and signs, from mild, limited in time, unifocal osteitis to severe, chronic, active or recurrent, multifocal osteomyelitis. In 2014 diagnostic criteria for were proposed, the Bristol Criteria Diagnosis Non-bacterial Osteitis, taking into account picture - location number inflammatory foci, characteristic changes on radiological...
The aim of this study was to evaluate if magnetic resonance imaging allows hip arthritis in JIA be differentiated from arthralgia unknown etiology juveniles clinically suspected for arthritis. This a retrospective observational which included 97 children with Each assessed and scored MRI signs active destructive inflammatory lesions developmental lesions. findings between JIA-confirmed patients without final diagnosis were compared the summarized score calculated, as sum scorings all 24 an...