Xanthogranulomatous pyelonephritis (XPN) is a rare and unusual form of pyelonephritis that infrequently occurs in renal allografts. Clinical presentation ranges from asymptomatic to fever, pyuria, and graft dysfunction. We present a case of a young African American male who presented with a marked elevation in serum creatinine from a baseline of 1.8-1.9 to 9.86 mg/dL. Transplant kidney biopsy was consistent with the diagnosis of XPN, showing xanthoma cells, which are pathognomonic for this condition. Following antibiotic treatment, allograft function improved and return to dialysis was averted. Clinicians should consider XPN in transplant patients with deteriorating allograft function, as its presentation can mimic more common conditions. Graft salvage with appropriate antimicrobial therapy should be attempted before considering nephrectomy which risks reinitiation of dialysis.
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http://dx.doi.org/10.1155/crit/6605652 | DOI Listing |
J Endourol
March 2025
Hospital Universitario "Dr. José Eleuterio González," Monterrey, Nuevo León, México.
Xanthogranulomatous pyelonephritis (XGP) is an infrequent, but life-threatening, chronic granulomatous pyelonephritis. Surgical intervention can be challenging because of severe inflammation and often a fibrotic reaction that obliterates anatomical landmarks. In addition, a high rate of open conversion has been reported when performing a laparoscopic nephrectomy.
View Article and Find Full Text PDFCase Rep Transplant
February 2025
Department of Nephrology, Hypertension and Transplant Medicine, Wellstar MCG Health, Augusta University, Augusta, Georgia, USA.
Xanthogranulomatous pyelonephritis (XPN) is a rare and unusual form of pyelonephritis that infrequently occurs in renal allografts. Clinical presentation ranges from asymptomatic to fever, pyuria, and graft dysfunction. We present a case of a young African American male who presented with a marked elevation in serum creatinine from a baseline of 1.
View Article and Find Full Text PDFXanthogranulomatous pyelonephritis (XGP) is a rare and diffusely destructive variant of pyelonephritis. Diagnosis is made using the characteristic radiological findings of renal enlargement with pelvicalyceal dilatation (the 'bear paw' sign) with histological analysis demonstrating replacement of renal parenchyma with foamy lipid-laden histiocytes. Treatment of XGP invariably requires nephrectomy.
View Article and Find Full Text PDFCureus
January 2025
Internal Medicine, Charleston Area Medical Center, Charleston, USA.
Xanthogranulomatous pyelonephritis (XGP) is a rare, chronic inflammatory renal disease typically caused by bacterial infections. We hereby report a rare case of bilateral XGP secondary to Candida albicans in a 31-year-old female with multiple autoimmune disorders. The patient presented with nonspecific abdominal discomfort, painful urination, and generalized weakness.
View Article and Find Full Text PDFNefrologia (Engl Ed)
February 2025
Sección de Nefrología Pediátrica, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.
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