Recurrent 2,8-Dihydroxyadenine Crystalline Nephropathy in Renal Allograft

Farid Arman; Russell John Crew; Michael Barry Stokes; Jai Radhakrishnan

doi:10.7326/aimcc.2023.1255

Annals of Internal Medicine: Clinical Cases (Jun 2024)

Recurrent 2,8-Dihydroxyadenine Crystalline Nephropathy in Renal Allograft

Farid Arman,
Russell John Crew,
Michael Barry Stokes,
Jai Radhakrishnan

Affiliations

Farid Arman: 1Division of Nephrology, Columbia University Medical Center, New York, New York
Russell John Crew: 1Division of Nephrology, Columbia University Medical Center, New York, New York
Michael Barry Stokes: 2Department of Pathology, Columbia University Medical Center, New York, New York
Jai Radhakrishnan: 1Division of Nephrology, Columbia University Medical Center, New York, New York

DOI: https://doi.org/10.7326/aimcc.2023.1255
Journal volume & issue: Vol. 3, no. 6

Abstract

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Adenine phosphoribosyltransferase deficiency is a rare cause of crystalline kidney disease. We present a case of end-stage kidney disease secondary to crystal deposition from adenine phosphoribosyltransferase deficiency with immediate recurrence of the crystals after transplantation.

Published in Annals of Internal Medicine: Clinical Cases

ISSN: 2767-7664 (Online)
Publisher: American College of Physicians
Country of publisher: United States
LCC subjects: Medicine: Internal medicine
Website: https://www.acpjournals.org/journal/aimcc

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