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Channel: 2020 Pediatric Rheumatology Symposium Archives - ACR Meeting Abstracts
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Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) Is Characterized by a...

Background/Purpose: Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) is characterized by abrupt onset of obsessive-compulsive disorder (OCD) and/or food restriction with other specified...

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Ongoing Disease Activity in Juvenile Idiopathic Arthritis (JIA) 18 Years...

Background/Purpose: Previously, we showed that ILAR JIA categories defined at disease onset change considerably during the first 8 years of disease course. Whether achieved remission and defined ILAR...

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Juvenile Spondyloarthritis in the Childhood Arthritis and Rheumatology...

Background/Purpose: To describe characteristics of children with enthesitis-related arthritis (ERA) and juvenile psoriatic arthritis (JPsA) enrolled in the Childhood Arthritis and Rheumatology Research...

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Defining the Prevalence of Depression and Anxiety Symptoms in Adolescents...

Background/Purpose: We aimed to evaluate the prevalence of depressive and/or anxiety symptoms in adolescents with juvenile idiopathic arthritis (JIA) and explore the association with demographic and...

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Protracted Febrile Myalgia Findings on Magnetic Resonance Imaging

Background/Purpose: Protracted febrile myalgia syndrome (PFMS) is a rare complication of familial Mediterranean fever (FMF) which consist of prolonged attack of fever, excruciating myalgia (up to 6...

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Pseudotumor Cerebri Syndrome in Children with Systemic Lupus Erythematosus

Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease that typically affects multiple organs and can lead to potentially fatal complications. Management of...

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Challenges Faced by Families of Children with an Auto-inflammatory Disease

Background/Purpose: Auto-inflammatory diseases (AIDs) are rare disorders that usually present in young children. Disease episodes, characterized by recurrent inflammation, are often frequent and...

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Resolution of Coronary Artery Changes in Patients with Refractory Kawasaki...

Background/Purpose: Treatment for patients with Kawasaki Disease (KD) refractory to standard therapy is controversial. Most experts recommend a second dose of IVIG [1], and for IVIG-resistant cases,...

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Clinical Features and Outcomes in Chronic Atypical Neutrophilic Dermatosis...

Background/Purpose: Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature (CANDLE) Syndrome is an autoinflammatory interferonopathy caused by mutations in the genes...

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Chronic Non-bacterial Osteomyelitis (CNO): Correlation Between Clinical and...

Background/Purpose: Due to the lack of widely accepted diagnostic criteria or disease biomarkers, chronic non-bacterial osteomyelitis (CNO) remains a diagnosis of exclusion. Whole-body MRI (WB-MRI) has...

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Chondrocytes Influence Fibroblast-like Synoviocytes from Patients with...

Background/Purpose: Juvenile Idiopathic Arthritis (JIA) progression leads to growth disturbances in affected joints. Fibroblast-like synoviocytes (FLS) play a key role in JIA pathogenesis; however, the...

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Cyclophosphamide Use in Treatment of Refractory Kawasaki Disease: A Single...

Background/Purpose: Intravenous immunoglobulin (IVIG) effectively treats vasculitis of the coronary arteries in the large majority of Kawasaki Disease (KD) patients. However, approximately 25% of...

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Feasibility and Pilot Study of Mental Health Screening in Juvenile Myositis

Background/Purpose: Juvenile myositis (JM) negatively affects health-related quality of life due to chronic weakness, skin/muscle damage, multiorgan dysfunction, and side effects of immunosuppression....

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Incidence, Contributing Factors, and Impact of Diagnostic Delay in Juvenile...

Background/Purpose: While early treatment of patients with newly diagnosed juvenile idiopathic arthritis (JIA) is an area of active study, delayed diagnosis of JIA is poorly characterized, with no...

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Treatment of Systemic Juvenile Idiopathic Arthritis in the CARRA Registry

Background/Purpose: The treatment of systemic juvenile idiopathic arthritis (SJIA) has changed dramatically over the past decade, associated with overall improvement in functional outcomes.  There may...

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Tubulointerstitial Nephritis and Uveitis (TINU): A Pediatric Case Series with...

Background/Purpose: Tubulointerstitial nephritis and uveitis (TINU) syndrome is an uncommon condition that is likely under-recognized. The ideal treatment of both renal and ophthalmologic disease...

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Perspectives of Radiologist Physicians in the Imaging of Chronic Nonbacterial...

Background/Purpose: Radiological imaging is integral to the diagnosis of chronic nonbacterial osteomyelitis (CNO) and has been included as a central component in suggested diagnostic criteria [1,2]....

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No-Shows: a Search for Modifiable Risk Factors

Background/Purpose: Missed ambulatory visits, or “no-shows,” limit patient access, increase costs, occupy provider time, and lead to worse patient outcomes. Only a few studies have been done in...

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Comparison of Efficacy Between Triamcinolone Acetonide and Hexacetonide...

Background/Purpose: The use of intra-articular corticosteroid (IAC) injections for Juvenile Idiopathic Arthritis (JIA) was extrapolated from its use in adult inflammatory joint diseases to achieve...

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A Preliminary Data-driven Anatomic Classification for Childhood Takayasu...

Background/Purpose: The pattern of arterial involvement and disease severity varies in those affected with cTA. Distinct imaging patterns that have some congruence with clinical phenotype may guide...

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