Severe Course of Primary Hyperoxaluria and Renal Failure After Domino Hepatic Transplantation
نویسندگان
چکیده
منابع مشابه
Hyperoxaluria After Renal Transplantation.
Primary hyperoxaluria is a rare autosomal recessive disorder, characterised by precipitation of insoluble oxalate crystals in the joints, kidneys, heart, eyes, skin, nerves, and bone marrow. The patients of primary oxaluria usually present with renal stone/nephrocalcinosis, and isolated kidney transplantation should not be done in these patients. We present a case report of 31-year lady with ac...
متن کاملDomino hepatic transplantation using the liver from a patient with primary hyperoxaluria.
BACKGROUND We report a case of domino liver transplantation using the liver harvested from a patient who underwent a combined liver and kidney transplantation for primary hyperoxaluria (PH). METHOD A cadaveric liver transplantation was performed in a 19-year-old man with PH. In a second step, the PH liver harvested from the first patient was transplanted in a 69-year-old man with hepatitis C-...
متن کاملSuccessful renal transplantation in primary hyperoxaluria.
A successful live related renal transplant in a 29-year-old male patient with Type 1 primary hyperoxaluria, who remains well 32 months postoperatively, is described. The plasma oxalate and exchangeable oxalate pool before transplantation were 160 mumol/1 and 4429 mumol respectively. Since the transplant these have been greatly reduced although they remain elevated above the normal by a factor o...
متن کاملRecurrence of primary hyperoxaluria after kidney transplantation.
Primary hyperoxaluria is a genetic disorder in glyoxylate metabolism that leads to systemic overproduction of oxalate. Functional deficiency of alanine-glyoxylate aminotransferase in this disease leads to recurrent nephrolithiasis, nephrocalcinosis, systemic oxalosis, and kidney failure. We present a young woman with end-stage renal disease who received a kidney allograft and experienced early ...
متن کاملCombined hepatic and renal transplantation in primary hyperoxaluria type I: clinical report of nine cases.
PURPOSE AND PATIENTS AND METHODS The purpose of this article is to report the experience of three centers with combined hepatic and renal transplantation for pyridoxine-resistant primary hyperoxaluria type I (alanine:glyoxylate aminotransferase [EC 2.6.1.44] deficiency), with particular emphasis on the selection criteria and timing of the operation. Nine patients with this inherited disease wer...
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ژورنال
عنوان ژورنال: American Journal of Transplantation
سال: 2005
ISSN: 1600-6135,1600-6143
DOI: 10.1111/j.1600-6143.2005.01014.x