Renal cystic diseases in children: New concepts

Pediatric Radiology

Volumn 40, Issue 6, 2010, Pages 939-946

  Avni, Fred E ^a   Hall, Michelle ^a  

^a ERASME HOSPITAL   (Belgium)

Author keywords

Child; Cyst; Kidney; MR; US

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 1BETA; T CELL FACTOR PROTEIN;

AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE; AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE; BARDET BIEDL SYNDROME; COMPUTER ASSISTED TOMOGRAPHY; CYSTIC DYSPLASIA; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; ECHOGRAPHY; GENE MUTATION; GLOMERULOCYSTIC KIDNEY; GLOMERULOCYSTIC KIDNEY DISEASE; GROUPS BY AGE; HEPATORENAL FIBROCYSTIC DISEASE; HUMAN; KIDNEY DISEASE; KIDNEY POLYCYSTIC DISEASE; NEPHRONOPHTISIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PERINATAL PERIOD; PRIORITY JOURNAL; REVIEW;

BELGIUM; CHILD; CHILD, PRESCHOOL; FEMALE; FORECASTING; HUMANS; INFANT; INFANT, NEWBORN; KIDNEY DISEASES, CYSTIC; MAGNETIC RESONANCE IMAGING; MALE; ULTRASONOGRAPHY;

EID: 77954431655     PISSN: 03010449     EISSN: 14321998     Source Type: Journal    
DOI: 10.1007/s00247-010-1599-5     Document Type: Review

References (40)

1. Ong AC, Weatley DN (2003) Polycystic kidney disease-the ciliary connection. Lancet 361:774-776
2. Gunay-Aygun M (2009) Liver and kidney disease in ciliopathies. Am J Med Genet Part C Semin Med Genet 151C:296-306
3. Bissler JJ, Dixon BP (2005) A mechanistic approach to inherited polycystic kidney disease. Pediatr Nephrol 20:558-566
4. Chiu MG, Johnson TM, Woolf AS et al (2006) Galectin-3 associated with the primary cilium and modulates cyst growth in congenital PKD. Amer J Pathol 169:1925-1938
5. Johnson CA, Gissen P, Sergi C (2003) Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes. J Med Genet 40:311-319
6. Hildebrandt F, Zhou W (2007) Nephronophtisis associated ciliopathies. J Am Soc Nephrol 18:1855-1871
7. Salomon R, Saunier S, Niaudet P (2009) Nephronophtisis. Pediatr Nephrol 24:2333-2344
8. Woolf AS, Feather SA, Bingham C (2002) Recent insights into kidney diseases associated with glomerular cysts. Pediatr Nephrol 17:229-235
9. Bisceglia M, Galliani CA, Senger C et al (2006) Renal cystic diseases: a review. Adv Anat Pathol 13:26-56
10. Edghill EL, Bingham C, Ellard S et al (2006) Mutations in hepatocyte nuclear factor-1β and their related phenotypes. J Med Genet 43:84-90
11. Ulinski T, Lescure S, Beaufils S et al (2006) Renal phenotypes related to Hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort. J Am Soc Nephrol 17:497-503
12. DeCramer S, Parant O, Beaufils S et al (2007) Anomalies of TCF2-gene are the main cause of fetal hyperechogenic kidneys. J Am Soc Nephrol 18:923-933
13. Edghill EL, Oram RA, Owens M et al (2008) Hepatocyte nuclear factor-1beta deletions a common cause of renal disease. Nephrol Dial Transplant 23:627-635
14. De Bruyn R, Gordon R (2000) Imaging in cystic renal disease. Arch Dis Child 83:401-407
15. Avni FE, Garel L, Cassart M et al (2006) Perinatal assessment of hereditary cystic renal diseases: the contribution of sonography. Pediatr Radiol 35:405-414
16. Rizk D, Chapman AB (2003) Cystic and inherited kidney diseases. Am J Kidney Dis 42:1305-1317
17. Deshpande C, Hennekam RCM (2008) Genetic syndromes and prenatally detected renal anomalies. Semin Fetal Neonatal Med 13:171-180
18. Winyard P, Chitty LS (2008) Dysplastic kidneys. Semin Fetal Neonatal Med 13:142-151
19. Cohen HL, Cooper J, Eisenberg P et al (1991) Normal length of fetal kidneys: sonographic study in 397 obsterric patients. AJR 157:545-548
20. De Bruyn R, Marks SD (2008) Post natal investigation of fetal renal disease. Semin Fetal Neonatal Med 12:133-141
21. Tsatsaris V, Gagnadoux MF, Aubry MC et al (2002) Prenatal diagnosis of bilateral isolated fetal hyperechogenic kidneys. It is possible to predict long-term outcome? BJOG 109:1388-1393
22. Chaumoitre K, Brun M, Cassart M et al (2006) Differential diagnosis of fetal hyperechogenic cystic kidneys unrelated to renal tract anomalies: a multicenter study. Ultrasound Obstet Gynecol 28:911-917
23. Ickowicz V, Eurin D, Maugey-Laulom B et al (2006) Meckel- Gruber syndrome:sonography and pathology. Ultrasound Obstet Gynecol 27:296-300
24. Cassart M, Eurin D, Didier F et al (2004)Antenatal renal sonographic anomalies and post-natal follow-up of renal involvement in Bardet- Biedl syndrome. Ultrasound Obstet Gynecol 24:51-54
25. Decramer S, Parant O, Beaufils S et al (2007) Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys. J Am Soc Nephrol 18:923-933
26. Brun M, Maugey-Laulom B, Eurin D et al (2004) Prenatal sonographic patterns in autosomal dominant polycystic kidney disease: a mulitcenter study. Ultrasound Obstet Gynecol 24:55-61
27. Slovis TL, Bernstein J, Gruskin A (1993) Hyperechoic kidneys in the newborn and young infant. Pediatr Nephrol 7:294-302
28. Nortier JL, Debiec H, Tournay Y et al (2006) Neonatal disease in neutral endopeptidase alloimmunization: lessons for immunological monitoring. Pediatr Nephrol 21:1399-1405
29. McHugh K, Stringer DA, Hebert D et al (1991) Simple renal cysts in children: diagnosis and follow-up with US. Radiology 178:383-385
30. Kuwertz-Broeking E, Brinkmann OA, Von Lengerke HJ et al (2004) Unilateral mulitcystic dysplastic kidney: experience in children. BJU Internat 93:388-392
31. Aslam M, Watson AR (2006) Unilateral mulitcystic dysplastic kidney: long-term outcomes. Arch Dis Child 91:820-823
32. Glazier DB, Fleisher MH, Cummings KB et al (1996) Cystic renal disease and tuberous sclerosis in children. Urology 48:613-615
33. Neumann HP, Schwarzkopf G, Henske EP (1998) Renal angiomyolipomas, cysts and cancer in TSC. Semin Pediatr Neurol 5:269-275
34. Cassart M, Massez A, Metens T et al (2004) Complementary role of MRI after sonography in assessing bilateral urinary tract anomalies in the fetus. AJR 182:684-695
35. Jaim M, LeQuesne GW, Bourne AJ et al (1997) High-resolution ultrasound in the differential diagnosis of cystic diseases of the kidney in infancy and childhood. J Ultrasound Med 16:235-240
36. Traubici J, Daneman A (2005) High-resolution renal sonography in children with autosomal recessive polycystic kidney disease. AJR 184:1630-1633
37. Lipschitz B, Berdon WE, Defelice AR et al (1993) Association of congenital hepatic fibrosis with autosomal dominant polycystic kidney disease. Report of a family with literature review. Pediatr Radiol 23:131-133
38. Premkumar A, Berdon WE, Levy J et al (1988) The emergence of hepatic fibrosis and portal hypertension in infants and children with autosomal recessive polycystic kidney disease. Initial and follow-up sonographic and radiographic findings. Pediatr Radiol 18:123-129
39. Avni EF, Guissard G, Hall M et al (2002) Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood. Pediatr Radiol 32:169-174
40. Turkbey B, Ocak I, Daryanani K et al (2009) Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF). Pediatr Radiol 39:100-111