A Case Study and Review of the Literature on IgA Nephropathy in Crohn's Disease
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT IgA nephropathy (IgAN) is the most frequently reported glomerular disease associated with inflammatory bowel disease (IBD), particularly Crohn's disease (CD), although pediatric cases remain rare. We report IgAN in a 16‐year‐old male with CD following intestinal surgery and during long‐term infliximab therapy, with renal impairment occurring ...
Giovanna Fernanda Vazzana +6 more
wiley +1 more source
Nodular glomerulosclerosis with anti-glomerular basement membrane-like glomerulonephritis; a distinct pattern of kidney injury observed in smokers [PDF]
, 2014 Background: Cigarette smoking has recently been recognized as a risk factor for developing nodular glomerulosclerosis and has also been frequently encountered in patients with anti-glomerular basement membrane (anti-GBM) disease.
Batal, Ibrahim +3 more
core +1 more source
Leveraging extracellular vesicle biology for novel tests and therapeutics for kidney fibrosis
Clinical and Translational Medicine, Volume 16, Issue 4, April 2026.Extracellular vesicles (EVs) are bilipid membrane‐encased nanoparticles that play critical roles as cell‐to‐cell messengers and waste management mechanisms. EVs cargos can be leveraged as biomarkers to develop minimally invasive tests for kidney fibrosis and guide personalised mechanism‐driven care.
Chin‐Ya Sophie Chiang +3 more
wiley +1 more source
MPO-ANCA associated crescentic glomerulonephritis with numerous immune complexes: case report
BMC Nephrology, 2012 Background Antineutrophil cytoplasmic antibody (ANCA)-associated crescentic glomerulonephritis (CGN) is a major cause of rapidly progressive glomerulonephritis (RPGN). ANCA-associated CGN is generally classified into pauci-immune RPGN, in which there are
Morizane Ryuji +8 more
doaj +1 more source
Pauci Immune crescentic glomerulonephritis in a patient with T-cell lymphoma and argyria [PDF]
, 2016 Background Silver is a transition metal, toxic when ingested in significant amounts, causing argyria (skin deposition) and argyrosis (eye deposition).
Cunningham, J +6 more
core
Clinical presentation and outcome of pediatric ANCA-associated glomerulonephritis [PDF]
, 2016 Background Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a small- and medium-sized vasculitis classically seen in adult patients, with peak onset near the fifth to seventh decade of life.
Andreoli, Sharon P., Kouri, Anne M.
core +1 more source
Cryptococcid Sweet Syndrome in the Setting of Hydralazine‐Induced ANCA Vasculitis: A Case Report
Journal of Cutaneous Pathology, Volume 53, Issue 4, Page 356-361, April 2026.ABSTRACT Acute febrile neutrophilic dermatosis, also known as Sweet syndrome, is an inflammatory skin condition characterized by the rapid onset of painful, erythematous plaques or nodules with neutrophilic infiltrate on histology. Rarely, acellular bodies surrounded by vacuolated spaces have been noted within the neutrophilic infiltrate, mimicking ...
Jenna Vroman +4 more
wiley +1 more source
Rare Bacteria Infecting the Heart and Affecting the Kidney of a Young Child
Case Reports in Nephrology and Dialysis, 2017 Rare bacteria can lead to infective endocarditis, which may lead to renal involvement as severe glomerulonephritis. We report our experience of a 12-year-old child who presented with infective endocarditis and blood culture-grown Gemella morbillorum – a ...
Gurinder Kumar +2 more
doaj +1 more source
Advanced Science, Volume 13, Issue 14, 9 March 2026.This review outlines association between vasculitis and malignancies and provides practical value for clinicians in distinguishing primary vasculitis from malignancy‐associated forms and optimizing patient surveillance, improving recognition of tumor‐associated vasculitis to reduce the risk of misdiagnosis, supporting more accurate clinical decision ...
Xiaofei Shi +8 more
wiley +1 more source
Immune complex type crescentic glomerulonephritis and ANCA-positivity in a nine-year-old girl
The Turkish Journal of Pediatrics, 2002 We report a nine-year-old girl who presented with the clinical and laboratory findings of rapidly progressive glomerulonephritis. She was found to be positive for both pANCA and cANCA.
Alper Soylu +4 more
doaj