Results 1 to 10 of about 1,213,222 (185)

Juvenile Systemic Lupus Erythematosus Presenting with Esophagitis and Severe Oral Mucositis [PDF]

Case Reports in Rheumatology, 2021
We present a case of a previously healthy adolescent female who developed severe oral mucositis and acute esophagitis as her presenting symptoms of juvenile systemic lupus erythematosus.
Emily Schildt, Kristen L Sessions, Deirdre De Ranieri   +2 more
doaj   +3 more sources

Juvenile systemic lupus erythematosus complicated with posterior reversible encephalopathy syndrome: a case report and literature review [PDF]

Orphanet Journal of Rare Diseases
Background Posterior reversible encephalopathy syndrome (PRES) is an acute or subacute neurological syndrome with clinical manifestations including headache, vision loss, altered mental status, and seizures.
Man Luo, Huan He, Qing Zhou, Long Chen, Changming Xia, GuoHua Yuan, Fang He   +6 more
doaj   +2 more sources

Unmasking Juvenile Systemic Lupus Erythematosus (JSLE): Multisystemic Manifestations in an Adolescent Male, A Rare Case Report [PDF]

Clinical Case Reports
Juvenile Systemic Lupus Erythematosus (JSLE) is a rare and chronic multisystem autoimmune condition with an accelerated course compared with adult‐onset SLE.
Shafaq Nazia, Aliza Andaleeb, Abdul Moiz, Hareem Ahmed, Muhammad Hassaan Javaid, Abubakr Mahmoud   +5 more
doaj   +2 more sources

Juvenile systemic lupus erythematosus presenting as pancarditis [PDF]

Pediatric Rheumatology Online Journal, 2019
Background Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with marked variation in its clinical presentation. Juvenile SLE (jSLE) accounts for 15–20% of all cases and is diagnosed when SLE manifests before 18 years of age. Pancarditis
D. O’Leary, C. O’Connor, L. Nertney, E. J. MacDermott, D. Mullane, O. Franklin, O. G. Killeen   +6 more
doaj   +2 more sources

Coexistence of Juvenile Systemic Lupus Erythematosus and Juvenile Spondyloarthropathy: A Case Report and Review of the Literature [PDF]

The Turkish Journal of Gastroenterology, 2020
Sacroiliitis has been scarcely reported in patients with systemic lupus erythematosus (SLE). In this article, we presented a pediatric case with coexis- tence of juvenile SLE and juvenile spondyloarthropathy (SpA) and discussed the clinical and ...
Ayşe TANATAR, Ummihan TOPAL, Şerife GÜL KARADAĞ, Hafize Emine SÖNMEZ, Nuray AKTAY AYAZ   +4 more
doaj   +2 more sources

The role of assessment of renal biopsy in electron microscopy in making a diagnosis of juvenile-onset systemic lupus erythematosus in a 16-year-old female patient with depression and proteinuria – case report

Central European Journal of Immunology, 2022
The course of juvenile-onset systemic lupus erythematosus may vary, from rapid multiorgan involvement to insidious development mimicking different medical conditions.
Tomasz Koszutski, Agnieszka Wiernik, Lidia Hyla-Klekot, Natalia Matysiak, Grażyna Kucharska   +4 more
doaj   +1 more source

Abstract 13 — Comparison of Clinical and Serological Features in Juvenile and Adult-Onset Systemic Lupus Erythematosus

Journal of Clinical Rheumatology and Immunology, 2023
Background Systemic lupus erythematosus (SLE) has varying clinical and serological features in juvenile and adult-onset disease groups, depending on the ethnicity. Objectives: To compare the disease characteristics of patients with adult-onset (ASLE) and
Babur Salim, Anum Khan, Haris Gul, Saba Samreen, Shahida Perveen   +4 more
doaj   +1 more source

Tumor necrosis factor receptor 2 and anti-ribosomal P antibodies as biomarkers in juvenile neuropsychiatric systemic lupus erythematosus

Journal of Radiation Research and Applied Sciences, 2022
Background: Neuropsychiatric systemic lupus erythematosus (NPSLE) is more frequent in adolescents than in adults and is indistinguishable from regular mood disorders. Aim: To investigate the levels of soluble tumor necrosis factor receptor 2 (sTNFR2) and
Hanan Ahmed Fathy, Manal Mohamed Alkady, Mohamed Said Tawfik   +2 more
doaj   +1 more source

Resolution of calcinosis using bisphosphonates in overlap syndrome – a case report

BMC Rheumatology, 2021
Introduction Calcinosis cutis is a common complication of pediatric rheumatologic diseases. However, there is currently no consensus on first-line treatment.
Mitchell Platter, Brian Pugmire, Reshma Patel   +2 more
doaj   +1 more source

Macrophage activation syndrome triggered by systemic lupus erythematosus flare: successful treatment with a combination of dexamethasone sodium phosphate, intravenous immunoglobulin, and cyclosporine: a case report

Journal of Medical Case Reports, 2021
Background Macrophage activation syndrome is classified as a secondary form of hemophagocytic lymphohistiocytosis. It is a hyperinflammatory complication observed to be comorbid with a variety of autoimmune diseases, including adult-onset Still’s disease
Wesam Gouda, Faisal Alsaqabi, Abdelhfeez Moshrif, Awad S. Abbas, Tarek M. Abdel-Aziz, Md Asiful Islam   +5 more
doaj   +1 more source