Literature DB >> 15077874

Four consecutive renal transplantations in a patient with adenine phosphoribosyltransferase deficiency.

P Eller1, A R Rosenkranz, W Mark, I Theurl, J Laufer, K Lhotta.   

Abstract

We report a patient with complete adenine phosphoribosyltransferase deficiency and urolithiasis, in whom 4 consecutive cadaveric renal transplantations were performed; 2,8-dihydroxyadenine crystal nephropathy recurred within weeks in the first and second graft when the patient was not treated with allopurinol immediately after transplantation. In the third graft, recurrence of disease could be prevented by immediate allopurinol treatment. This graft was lost due to chronic allograft nephropathy without significant crystal deposition. After a fourth transplantation, again without initial allopurinol, the disease recurred following an initial vascular rejection. Addition of allopurinol significantly improved renal function of the 2nd and 4th graft. This case indicates that outcome of renal transplantation in patients with adenine phosphoribosyltransferase deficiency critically depends on immediate postoperative pharmacotherapy with allopurinol, which is able to prevent 2,8-dihydroxyadenine nephropathy in the graft. Furthermore, rapid recurrence of disease without allopurinol seems to be triggered by delayed graft function and acute rejection.

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Year:  2004        PMID: 15077874     DOI: 10.5414/cnp61217

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  11 in total

1.  A rare case of primary non-function of renal allograft due to adenine phosphoribosyltransferase deficiency.

Authors:  Benoit Brilland; Jean-François Augusto; Anne Croue; Jean-François Subra; Johnny Sayegh
Journal:  Int Urol Nephrol       Date:  2015-08-09       Impact factor: 2.370

2.  Adenine phosphoribosyltransferase deficiency in children.

Authors:  Jérôme Harambat; Guillaume Bollée; Michel Daudon; Irène Ceballos-Picot; Albert Bensman
Journal:  Pediatr Nephrol       Date:  2012-01-03       Impact factor: 3.714

3.  Kidney Disease in Adenine Phosphoribosyltransferase Deficiency.

Authors:  Hrafnhildur Linnet Runolfsdottir; Runolfur Palsson; Inger M Agustsdottir; Olafur S Indridason; Vidar O Edvardsson
Journal:  Am J Kidney Dis       Date:  2015-12-25       Impact factor: 8.860

4.  Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiency.

Authors:  Guillaume Bollée; Cécile Dollinger; Lucile Boutaud; Delphine Guillemot; Albert Bensman; Jérôme Harambat; Patrice Deteix; Michel Daudon; Bertrand Knebelmann; Irène Ceballos-Picot
Journal:  J Am Soc Nephrol       Date:  2010-02-11       Impact factor: 10.121

5.  Crystalline Nephropathy due to APRT Deficiency: A Preventable Cause of Renal and Renal Allograft Failure.

Authors:  Prashant Rajput; Zaheer A Virani; Bharat V Shah
Journal:  Indian J Nephrol       Date:  2020-04-01

6.  Recurrent 2,8-dihydroxyadenine nephropathy: a rare but preventable cause of renal allograft failure.

Authors:  M Zaidan; R Palsson; E Merieau; E Cornec-Le Gall; A Garstka; U Maggiore; P Deteix; M Battista; E-R Gagné; I Ceballos-Picot; J-P Duong Van Huyen; C Legendre; M Daudon; V O Edvardsson; B Knebelmann
Journal:  Am J Transplant       Date:  2014-10-10       Impact factor: 8.086

7.  Shedding light on the chemical diversity of ectopic calcifications in kidney tissues: diagnostic and research aspects.

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Journal:  PLoS One       Date:  2011-11-18       Impact factor: 3.240

8.  Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation.

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Journal:  NDT Plus       Date:  2010-06-02

9.  Kidney Transplant Outcomes in Patients With Adenine Phosphoribosyltransferase Deficiency.

Authors:  Hrafnhildur Linnet Runolfsdottir; Runolfur Palsson; Inger M Sch Agustsdottir; Olafur S Indridason; Jennifer Li; Myriam Dao; Bertrand Knebelmann; Dawn S Milliner; Vidar O Edvardsson
Journal:  Transplantation       Date:  2020-10       Impact factor: 5.385

10.  Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management.

Authors:  Jiwon Jung; Joo Hoon Lee; Young Seo Park; Go Hun Seo; Changwon Keum; Hee Gyung Kang; Hajeong Lee; Sang Koo Lee; Sang Taek Lee; Heeyeon Cho; Beom Hee Lee
Journal:  BMC Med Genomics       Date:  2021-07-03       Impact factor: 3.063

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