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http://dx.doi.org/10.1016/j.nefro.2015.04.005 | DOI Listing |
Am J Kidney Dis
December 2024
Nephrology and Dialysis Unit, Meyer Children's Hospital IRCCS, Firenze, Italy; Department of Biomedical, Experimental and Clinical Sciences "Mario Serio", University of Firenze, Firenze, Italy. Electronic address:
Case Rep Nephrol Dial
March 2024
Nephrology Service, Hospital General de México, Mexico City, Mexico.
Introduction: The presence of three different entities in a single patient is usually of clinical interest and mostly anecdotal. The overlap of systemic sclerosis (SSc), Sjögren syndrome (SS), and ANCA-associated renal-limited vasculitis has been reported only once previously.
Case Presentation: A 61-year-old female was evaluated at consultation with 2 years of symptomatology, presenting cardboard-like skin, sclerodactyly, limited oral opening, and dry skin and eyes.
Nefrologia (Engl Ed)
December 2023
Hospital Clínico San Carlos, Ciudad Real, Spain.
Med Clin (Barc)
February 2024
Sección de Nefrología, Hospital Universitario San Agustín, Avilés, Asturias, España.
Pediatr Nephrol
March 2024
Division of Nephrology, Hôpital Robert Debré, Paris, France.
Background: Tubulointerstitial lesions and glomerular inflammation severity have been shown to correlate with proteinuria in children with IgA nephropathy (cIgAN). However, there is a lack of data regarding severity of histopathologic findings in cIgAN in patients with minimal to absent proteinuria since kidney biopsy indications are not well defined in these cases.
Methods: Twenty-eight cIgAN patients with kidney biopsy from 4 different centers in Paris (France) and Montreal (Canada) with a urine protein/creatinine ratio (UPCr) ≤ 0.
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