ReviewInternational journal of pediatrics2013
Kidney and urinary tract involvement in kawasaki disease.
Review in International journal of pediatrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
26 citing papers in PubMed, 52 citations in OpenAlex.
- A triad of hypertension, heart failure, and glomerular injury in subacute Kawasaki disease: a case report and literature review.Frontiers in cardiovascular medicine · 2026Article
- Human pathological findings in Kawasaki disease: a narrative review of autopsy and biopsy evidence.Frontiers in immunology · 2026Review
- Value of cystatin C for Kawasaki disease with coronary artery aneurysm.Translational pediatrics · 2025Article
- Endothelial Dysfunction: Molecular Mechanisms and Therapeutic Strategies in Kawasaki Disease.International journal of molecular sciences · 2024Review
- Use of Machine Learning to Differentiate Children With Kawasaki Disease From Other Febrile Children in a Pediatric Emergency Department.JAMA network open · 2023Article
- Overlap of C3 Glomerulopathy and Thrombotic Microangiopathy: A Case Series.Kidney international reports · 2023Article
- Clinical Manifestations and Laboratory Findings of Kawasaki Disease: Beyond the Classic Diagnostic Features.Medicina (Kaunas, Lithuania) · 2022Review
- Nontypical presentation of a common disease: a case report.Journal of medical case reports · 2022Article
- Prominent gallbladder enlargement: Kawasaki disease or other congenital or acquired gallbladder disease? A case report.The Journal of international medical research · 2021Article
- Kawasaki Disease and Acute Kidney Injury in Pediatric Patients.Indian journal of pediatrics · 2021Article
- Atypical Kawasaki Disease in an Adolescent with Multivisceral Involvement.Case reports in pediatrics · 2021Article
- Kawasaki disease: pathophysiology and insights from mouse models.Nature reviews. Rheumatology · 2020Review
- Familial Kawasaki disease and acute glomerulonephritis: case report and review of literature.Sudanese journal of paediatrics · 2020Article
- Atypical manifestations of cardiomegaly and nephrotic syndrome in Kawasaki disease: Two case reports.Medicine · 2019Article
- Unusual Presentation Of Kawasaki Disease With Gastrointestinal And Renal Manifestations.Therapeutics and clinical risk management · 2019Article
- Early features of Kawasaki disease with pyuria in febrile infants younger than 6 months.BMC pediatrics · 2018Article
- Clinical features of acute kidney injury in patients with Kawasaki disease.World journal of clinical pediatrics · 2018Review
- Molecular basis of coronary artery dilation and aneurysms in patients with Kawasaki disease based on differential protein expression.Molecular medicine reports · 2018Article
- Acute kidney injury occurs only rarely in patients with Kawasaki disease.Pediatric research · 2017Article
- An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Answers.Pediatric nephrology (Berlin, Germany) · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Kawasaki disease (KD) is a systemic vasculitis and can develop multiple organ injuries including kidney and urinary tract involvement. These disorders include pyuria, prerenal acute kidney injury (AKI), renal AKI caused by tubulointerstitial nephritis (TIN), hemolytic uremic syndrome (HUS), and immune-complex mediated nephropathy, renal AKI associated with either Kawasaki disease shock syndrome or unknown causes, acute nephritic syndrome (ANS), nephrotic syndrome (NS), renal tubular abnormalities, renal abnormalities in imaging studies, and renal artery lesions (aneurysms and stenosis). Pyuria is common in KD and originates from the urethra and/or the kidney. TIN with AKI and renal tubular abnormalities probably result from renal parenchymal inflammation caused by T-cell activation. HUS and renal artery lesions are caused by vascular endothelial injuries resulting from vasculitis. Some patients with ANS have immunological abnormalities associated with immune-complex formation. Nephromegaly and renal parenchymal inflammatory foci are detected frequently in patients with KD by renal ultrasonography and renal scintigraphy, respectively. Although the precise pathogenesis of KD is not completely understood, renal vasculitis, immune-complex mediated kidney injuries, or T-cell immune-regulatory abnormalities have been proposed as possible mechanisms for the development of kidney and urinary tract injuries.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.