Results 31 to 40 of about 12,435 (203)

Anti-Glomerular Basement Membrane Disease in a 10-year-old Child: A Case Report

open access: yesJournal of Nepal Medical Association, 2023
Anti-glomerular basement membrane disease is an extremely uncommon entity in children. It has an incidence of 0.5 to 1 per million per year in adults and is even more uncommon in children.
Md Firoz Anjum   +4 more
doaj   +1 more source

Overlapping Syndromes: Drug-Induced Vasculitis From Hydralazine With Positive Antinuclear Antibodies

open access: yesClinical Medicine Insights: Case Reports, 2023
Hydralazine is an antihypertensive medication that has been associated with drug-associated autoimmune syndromes like interstitial lung disease, pauci-immune glomerulonephritis, and hypocomplementemia.
Lakshmi Kannan, UmmeRubab Syeda
doaj   +1 more source

Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature

open access: yesBrazilian Journal of Nephrology, 2021
Rapidly progressive glomerulonephritis is a medical emergency, with mortality around 20%. It is characterized by crescent glomerulonephritis and progressive loss of kidney function, hematuria, and proteinuria.
Carlos Mauricio Martínez Montalvo   +4 more
doaj   +2 more sources

Rapidly Progressive Glomerulonephritis: Etiology, Treatment, and Prognosis: A Review Literature [PDF]

open access: yesTranslational Research in Urology
Rapidly progressive glomerulonephritis (RPGN) is define the following: 1. Fast damage of kidney function temporary (days to weeks). 2. Macro or microscopic hematuria, proteinuria, dysmorphic red blood cells (RBC). 3. Renal biopsy showed cellular crescent
Ziba Aghsaeifard, Setareh Zahedian
doaj   +1 more source

A 5-year retrospective study to determine the spectrum of crescentic glomerulonephritis in three tertiary hospitals in Gauteng Province, South Africa

open access: yesSouth African Medical Journal
Background. Rapidly progressive glomerulonephritis is a clinical syndrome that results in rapid decline in kidney function over a period of weeks to months. Its histological hallmark is extensive crescent formation. Objective. To determine the causes of
S Meel
doaj   +1 more source

What is new in the management of rapidly progressive glomerulonephritis?

open access: yes, 2015
Rapidly progressive glomerulonephritis (RPGN) results from severe crescentic damage to glomeruli and leads to irreversible kidney failure if not diagnosed and managed in a timely fashion.
Greenhall, GHB   +3 more
core   +1 more source

Predictors of rapidly progressive glomerulonephritis in acute poststreptococcal glomerulonephritis

open access: yes, 2023
Background Acute post-streptococcal glomerulonephritis (APSGN) is an immune-mediated inflammatory respsonse in the kidneys caused by nephritogenic strains of group A (3-hemolytic streptococcus (GAS).
Sait Can Yücebaş   +13 more
core   +1 more source

Fibrillary Glomerulonephritis Diagnosis Is Enhanced by DNAJB9: Three Cases with Different Clinical, Anatomopathologic Features and Outcomes

open access: yesPathophysiology
Background: Fibrillary glomerulonephritis (FGN) is a rare and poorly understood kidney disease characterized by the deposition of non-amyloid fibrils in the glomeruli.
José C. De La Flor   +8 more
doaj   +1 more source

Serum sulfatide level is associated with severe systemic vasculitis with kidney involvement

open access: yesFrontiers in Immunology, 2023
Sulfatides are a type of sulfated glycosphingolipid that are secreted with lipoproteins into the serum. These molecules are involved in the inflammatory pathway of vessels in addition to coagulation and platelet aggregation.
Daiki Aomura   +11 more
doaj   +1 more source

Rapidly progressive glomerulonephritis due to IgA nephropathy accompanied by collagenofibrotic glomerulopathy. A nephrology picture. [PDF]

open access: yesJ Nephrol
Citation: Ochiai, S., Kikuchi, M., Kaikita, K. et al. Rapidly progressive glomerulonephritis due to IgA nephropathy accompanied by collagenofibrotic glomerulopathy. A nephrology picture. J Nephrol (2024). https://doi.org/10.1007/s40620-023-01875-
Ochiai S   +3 more
europepmc   +2 more sources

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