Literature DB >> 15547226

Type 1 primary hyperoxaluria in pediatric patients: renal sonographic patterns.

Ousséini Diallo1, Françoise Janssens, Michelle Hall, E Fred Avni.   

Abstract

OBJECTIVE: Our aim was to review the sonographic features of type I primary hyperoxaluria in children and to correlate the sonographic patterns with the clinical development of end-stage renal disease (ESRD).
MATERIALS AND METHODS: We performed a retrospective analysis of the clinical and imaging files of 13 patients with type I primary hyperoxaluria who were treated in one institution and of the sonographic patterns and the clinical follow-up reports.
RESULTS: We encountered the following two sonographic patterns: medullary nephrocalcinosis in eight patients and cortical nephrocalcinosis in five patients. The sonographic appearance of cortical nephrocalcinosis is quite specific: a hyperechoic peripheral renal cortex with acoustic shadowing behind it. Medullary nephrocalcinosis is less specific because there are many other causes of hyperechoic pyramids. All patients with medullary nephrocalcinosis developed lithiasis during the course of the disease. All patients with cortical nephrocalcinosis but only two of eight with medullary nephrocalcinosis developed ESRD.
CONCLUSION: Sonography can be used differentiate the two patterns of type 1 primary hyperoxaluria. The cortical nephrocalcinosis type carries a higher risk of developing ESRD.

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Year:  2004        PMID: 15547226     DOI: 10.2214/ajr.183.6.01831767

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  7 in total

1.  Cortical nephrocalcinosis in an infant caused by primary hyperoxaluria type 1.

Authors:  Anil Gopalakrishna Rao
Journal:  Pediatr Radiol       Date:  2010-10-16

Review 2.  Quantitation of stone burden: imaging advances.

Authors:  Terri J Vrtiska
Journal:  Urol Res       Date:  2005-11-13

Review 3.  Primary hyperoxaluria: spectrum of clinical and imaging findings.

Authors:  Sara B Strauss; Temima Waltuch; William Bivin; Frederick Kaskel; Terry L Levin
Journal:  Pediatr Radiol       Date:  2016-11-14

4.  A rare case of primary hyperoxaluria type 1 co-existing with autosomal-dominant polycystic kidney disease in a newborn.

Authors:  Arnaud Devriendt; Nash Damry; Michèle Hall; Maria Mesquita; Fred Avni
Journal:  Pediatr Radiol       Date:  2010-05-19

Review 5.  Oxalosis in primary hyperoxaluria in infancy : Report of a case in a 3-month-old baby. Follow-up for 3 years and review of literature.

Authors:  Cinzia Orazi; Stefano Picca; Paolo M S Schingo; Fausto M Fassari; Giuseppe Canepa
Journal:  Skeletal Radiol       Date:  2009-01-09       Impact factor: 2.199

6.  Stony kidneys in a child: Clue to a rare diagnosis.

Authors:  A Mukund; P Gupta; S Gamanagatti
Journal:  Indian J Nephrol       Date:  2011-10

7.  Primary hyperoxaluria.

Authors:  Jérôme Harambat; Sonia Fargue; Justine Bacchetta; Cécile Acquaviva; Pierre Cochat
Journal:  Int J Nephrol       Date:  2011-06-16
  7 in total

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