Case Report
Year 2017,
Volume: 56 Issue: 4, 203 - 205, 01.12.2017
Abstract
Hiperoksalüri nefrolithiazis ve nefrokalsinozis ile karakterize, idrardaki kalsiyum oksalatın süpersatürasyonu sonucu oluşur. Kalsiyum oksalat depozitleri böbrek hasarı, böbrek yetmezliği ve diğer organlarda hasarlanmaya neden olabilir. Burada nadir de olsa ciddi bir durum arz eden, renal özellikleri açısından şüphelenilebilen primer hiperoksalüri vakasını sunduk. Radyolojik iskelet değişiklikleri oldukça spesifik olmakla birlikte renal osteodistrofi ile benzer özellikler taşıyabilir.
Keywords
References
- Danpure CJ. Genetic disorders and urolithiasis. Urol Clin North Am 2000;27(2):287-99.
- Alkhunaizi A, Chan L Secondary oxalosis: A cause of delayed recovery of renal function in the setting of acute renal failure. J Am Soc Nephrol 1996;7(11):2321-6.
- Cochat P, Basmaison O. Current approaches to the management of primary hyperoxaluria. Arch Dis Child 2000;82(6):470-3.
- Bensman A, Legendre C, Palomera S, Thervet E, Kreis H. How to treat primary oxalosis? Nephrol Dial Transplant 1995;11(2):394-5.
- Jamieson NV. The European Primary Hyperoxaluria Type 1 Transplant Registry Report on the results of combined liver and kidney transplantation for primary hyperoxaluria 1984-1994. Nephrol Dial Transplant 1995;10(8):33-7.
- Cochat P, Sharer K. Should liver transplantation be performed before advanced renal insufficiency in primary hyperoxaluria type1? Pediatr Nephrol 1993;7(2):212-3.
- Ring E, Wendler H, Ratschek M, Zobel G. Bone disease of primary hyperoxaluria in infancy. Pediatr Radiol 1989;20(1):131-3.
- Wiggelinkhuizen J, Fisher RM. Oxalosis of bone. Pediatr Radiol 1982;12:307-9.
- Day DL, Scheinman JI, Mahan J. Radiological aspects of primary hyperoxaluria. AJR 1986;146(2):395-401.
Year 2017,
Volume: 56 Issue: 4, 203 - 205, 01.12.2017
Abstract
Hyperoxaluria is characterized by nephrolithasis and nephrocalcinosis caused by supersaturation of calcium oxalate
in the urine. Deposits of calcium oxalate can lead to kidney damage, kidney failure, and injury to other organs.
Herein, we report a case of primary hyperoxaluria which is a serious though rare condition, can be suspected on the
basis of the renal features. Radiological skeletal changes, which are also rather specific, may also share some
features with renal osteodystrophy.
Keywords
References
- Danpure CJ. Genetic disorders and urolithiasis. Urol Clin North Am 2000;27(2):287-99.
- Alkhunaizi A, Chan L Secondary oxalosis: A cause of delayed recovery of renal function in the setting of acute renal failure. J Am Soc Nephrol 1996;7(11):2321-6.
- Cochat P, Basmaison O. Current approaches to the management of primary hyperoxaluria. Arch Dis Child 2000;82(6):470-3.
- Bensman A, Legendre C, Palomera S, Thervet E, Kreis H. How to treat primary oxalosis? Nephrol Dial Transplant 1995;11(2):394-5.
- Jamieson NV. The European Primary Hyperoxaluria Type 1 Transplant Registry Report on the results of combined liver and kidney transplantation for primary hyperoxaluria 1984-1994. Nephrol Dial Transplant 1995;10(8):33-7.
- Cochat P, Sharer K. Should liver transplantation be performed before advanced renal insufficiency in primary hyperoxaluria type1? Pediatr Nephrol 1993;7(2):212-3.
- Ring E, Wendler H, Ratschek M, Zobel G. Bone disease of primary hyperoxaluria in infancy. Pediatr Radiol 1989;20(1):131-3.
- Wiggelinkhuizen J, Fisher RM. Oxalosis of bone. Pediatr Radiol 1982;12:307-9.
- Day DL, Scheinman JI, Mahan J. Radiological aspects of primary hyperoxaluria. AJR 1986;146(2):395-401.
There are 9 citations in total.
Details
| Primary Language | English |
|---|---|
| Subjects | Health Care Administration |
| Journal Section | Case Reports |
| Authors | |
| Publication Date | December 1, 2017 |
| Submission Date | July 15, 2016 |
| Published in Issue | Year 2017Volume: 56 Issue: 4 |
