Abstract
Hyperoxaluria is characterized by nephrocalcinosis and nephrolithiasis on radiological examination and may also result in diffuse deposition of calcium oxalate crystals in multiple extrarenal organs (oxalosis). In two cases, the renal findings of primary hyperoxaluria were diagnosed by ultrasound and computed tomography scans. In addition to renal involvement, both patients had liver involvement, and one patient had cardiac involvement.
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Williams HE, Smith LH Jr (1982) Primary hyperoxaluria. In: Stanbury JB, Wyngaarden JB, Frederickson DS, Goldstein JL, Brown MS (eds) The metabolic bases of inherited diseases, 5th edn. McGraw-Hill, New York, pp 204–228
Day DL, Scheinman JI, Mahan J (1986) Radiological aspects of primary hyperoxaluria. AJR 146:395–401
Brennan JN, Diwan RJ, Makker SP, Cromer BA, Bellon EM (1982) Ultrasonic diagnosis of primary hyperoxaluria in infancy. Radiology 145:147–148
Srinivas HN, Ramkumar C (1986) Primary hyperoxaluria in infancy. Australas Radiol 30:332–334
Spiers EM, Sanders DY, Omura E (1990) Clinical and histological features of primary hyperoxalosis. J Am Acad Dermatol 22:952–956
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Akhan, O., Özmen, M.N., Coşkun, M. et al. Systemic oxalosis: Pathognomonic renal and specific extrarenal findings on US and CT. Pediatr Radiol 25, 15–16 (1995). https://doi.org/10.1007/BF02020832
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DOI: https://doi.org/10.1007/BF02020832