Results 31 to 40 of about 1,613,455 (162)

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

Clinical 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

Rapidly Progressive Glomerulonephritis Associated with Nontuberculous Mycobacteria [PDF]

, 2007
A 72-year-old woman with a past medical history of nontuberculous mycobacteria (NTM) pulmonary disease was admitted because of hemoptysis and acute renal failure. A chest X-ray showed interstitial infiltration over bilateral lung fields.
Wen, Yao-Ko, Chen, Shwu-Jiuan, Chen, Mei-Ling   +2 more
core   +1 more source

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

Brazilian 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, Laura Catalina Gutierrez, Carolina Perez, Harrison Herrera Delgado, Paula Corinna Martinez Barrios   +4 more
doaj   +2 more sources

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

Translational 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

Clinical Features of Rapidly Progressive Alzheimer's Disease [PDF]

, 2010
Objective: To characterize clinical features, CSF biomarkers and genetic polymorphisms of patients suffering from a rapidly progressing subtype of Alzheimer's dementia (rpAD).
Meissner, Bettina, Bettina Meissner, Zerr, Inga, Redyk, Katharina, Christian Schmidt, Nico von Ahsen, Kretzschmar, Hans A., Lennart Krack, Schmidt, Christian, Roeber, Sigrun, von Ahsen, Nico, Katharina Redyk, Sigrun Roeber, Hans Kretzschmar, Inga Zerr, Krack, Lennart, Kretzschmar, Hans, Schmidt, Christian D., Krack, Lennart A., Ahsen, Nico von   +19 more
core   +1 more source

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

J 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, Kikuchi M, Kaikita K, Fujimoto S.   +3 more
europepmc   +3 more sources

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

South 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

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

Frontiers 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, Makoto Harada, Takero Nakajima, Takero Nakajima, Takayuki Nimura, Kosuke Yamaka, Yosuke Yamada, Koji Hashimoto, Naoki Tanaka, Naoki Tanaka, Naoki Tanaka, Yuji Kamijo   +11 more
doaj   +1 more source

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

Pathophysiology
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, Marco Dominguez Davalos, Tania Linares Grávalos, Marina Alonso-Riaño, Francisco Díaz, Celia Rodríguez Tudero, Rocío Zamora González-Mariño, Michael Cieza Terrones, Jesús Hernández Vaquero   +8 more
doaj   +1 more source

Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease

, 2015
Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day).

core   +1 more source