Renal tumours in early life

Current Diagnostic Pathology

Volumn 12, Issue 3, 2006, Pages 210-219

  Vujanić, Gordan M ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

Clear cell sarcoma; Infancy; Mesoblastic nephroma; Renal tumours; Rhabdoid tumour; Wilms' tumour

Indexed keywords

ARTICLE; CANCER SURGERY; CHILDHOOD CANCER; CLEAR CELL SARCOMA; DIAGNOSTIC ACCURACY; HUMAN; INFANCY; KIDNEY TUMOR; MESOBLASTIC NEPHROMA; NEPHROBLASTOMA; RHABDOID TUMOR;

EID: 33646894297     PISSN: 09686053     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cdip.2006.03.003     Document Type: Article

References (42)

1. Moore S.W., Satge D., Sasco A.J., et al. The epidemiology of neonatal tumours. Pediatr Surg Int 19 (2003) 509-519
2. Hrabovsky E.E., Othersen H.B., deLorimier A., Kelalis P., Beckwith J.B., and Takashima J. Wilms' tumor in the neonates: a report from the national Wilms' Tumor Study. J Pediatr Surg 21 (1986) 385-387
3. Ritchey M.L., Azizkhan R.G., Beckwith J.B., et al. Neonatal Wilms tumor. J Pediatr Surg 30 (1995) 856-859
4. Beckwith J.B. Renal tumors. In: Stocker J.T., and Askin F.B. (Eds). Pathology of solid tumors in children (1999), Chapman & Hall Medical, London 1-23
5. Leclair M.D., El-Ghoneimi A., Audry G., et al. The outcome of prenatally diagnosed renal tumors. J Urol 173 (2005) 186-189
6. Angulo J.C., Lopez J.I., Ereno C., et al. Hydrops fetalis and congenital mesoblastic nephroma. Child Nephrol Urol 11 (1991) 115-116
7. Miller O.F., and Kolon T.F. Hyperreninemia and congenital mesoblastic nephroma: case report and review of the literature. Urology 55 (2000) 775xxv-775xxvii
8. Jayabose S., Iqbal K., Newman L., et al. Hypercalcemia in childhood renal tumors. Cancer 61 (1988) 788-791
9. Birch J.M., and Breslow N. Epidemiologic features of Wilms tumor. Hematol Oncol Clin North Am 9 (1995) 1157-1178
10. Kalapurakal J.A., Nan B., Norkool P., et al. Treatment outcomes in adults with favourable histologic type Wilms tumor-an update from the National Wilms Tumor Study Group. Int J Radiat Oncol Biol Phys 60 (2004) 1379-1384
11. Ritchey M.L., and Coppes M.J. The management of synchronous bilateral Wilms tumor. Hematol Oncol Clin North Am 9 (1996) 1303-1316
12. Coppes M.J., Wilson P.C., and Weitzman S. Extrarenal Wilms' tumor: staging, treatment and prognosis. J Clin Oncol 9 (1991) 167-174
13. Ruteshouser E.C., and Huff V. Familial Wilms tumor. Am J Med Genet 129C (2004) 29-34
14. Grundy P.E., Breslow N.E., Li S., et al. Loss of heterozygosity for chromosome 1p and 16q is an adverse prognostic factor in favourable-histology Wilms tumor: a report from the National Wilms Tumor Study Group. J Clin Oncol 23 (2005) 7312-7321
15. Murphy WM, Grignon DJ, Perlman EJ. (Eds.), Kidney tumors in children. In: Atlas of tumor pathology, 4th Series, Fascicle 1. Washington, DC: Armed Forces Institute of Pathology; p. 47-9.
16. Vujanic G.M., Sandstedt B., Harms D., Kelsey A., Leuschner I., and de Kraker J. Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood. Med Pediatr Oncol 38 (2001) 79-82
17. Green D.M., Breslow N.E., Beckwith J.B., et al. Treatment with nephrectomy only for small, stage I/favourable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group. J Clin Oncol 19 (2001) 3719-3724
18. Pritchard-Jones K., Kelsey A., Vujanic G., Imeson J., Hutton C., and Mitchell C. Older age is an adverse prognostic factor in stage I, favorable histology Wilms' tumor treated with vincristine monochemotherapy: a study by the United Kingdom Children's Cancer Study Group, Wilms' Tumor Working Group. J Clin Oncol 21 (2003) 3269-3275
19. Weirich A., Leuschner I., Harms D., et al. Clinical impact of histologic subtypes in localized non-anaplastic nephroblastoma treated according to the trial and study SIOP-9/GPOH. Ann Oncol 12 (2001) 311-319
20. Beckwith J.B., Zuppan C.E., Browning N.G., Moksness J., and Breslow N.E. Histologic analysis of aggressiveness and responsiveness in Wilms' tumor. Med Pediatr Oncol 27 (1996) 422-428
21. Maes P., Delemarre J., de Kraker J., and Ninane J. Fetal rhabdomyomatous nephroblastoma: a tumor of good prognosis but resistant to chemotherapy. Eur J Cancer 35 (1999) 1356-1360
22. Beckwith J.B. Precursor lesions of Wilms tumor: clinical and biological implications. Med Pediatr Oncol 21 (1993) 158-168
23. Coppes M.J., Arnold M., Beckwith J.B., et al. Factors affecting the risk of contralateral Wilms tumor development: a report from the National Wilms Tumor Study Group. Cancer 85 (1999) 1616-1625
24. Joshi V.V., and Beckwith J.B. Multilocular cyst of the kidney (cystic nephroma) and cystic, partially differentiated nephroblastoma. Terminology and criteria for diagnosis. Cancer 64 (1989) 466-479
25. Blakely M.L., Shamberger R.C., Norkool P., et al. Outcome of children with cystic partially differentiated nephroblastoma treated with and without chemotherapy. J Pediatr Surg 38 (2003) 897-900
26. Vujanic G.M., Sandstedt B., Dijoud F., Harms D., and Delemarre J.F.M. Nephrogenic rest associated with a mesoblastic nephroma-what does it tell us?. Pediatr Pathol Lab Med 15 (1995) 469-475
27. Sutherland R.W., Weiner J.S., Hicks M.J., Hawkins E.P., and Chintagumpala M. Congenital mesoblastic nephroma in a child with the Beckwith-Wiedemann syndrome. J Urol 158 (1997) 1532-1533
28. Shao L., Hill D.A., and Perlman E.J. Expression of WT-1, Bcl-2, and CD34 by primary renal spindle cell tumors in children. Pediatr Dev Pathol 7 (2004) 577-582
29. Knezevich S.R., Garnett M.J., Pysher T.J., et al. ETV6-NTRK3 gene fusion and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma. Cancer Res 58 (1998) 5046-5048
30. Rubin B.P., Chen C.J., Morgan T.W., et al. Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma. Am J Pathol 153 (1998) 1451-1458
31. In: Beckwith J.B. (Ed). Letter to editor. Pediatr Pathol 13 (1993) 885-887
32. Argani P., and Beckwith J.B. Metanephric stromal tumor. Report of 31 cases of a distinctive pediatric renal neoplasm. Am J Surg Pathol 24 (2000) 917-926
33. Argani P., Perlman E.J., Breslow N.E., et al. Clear cell sarcoma of the kidney: a review of 351 cases from the National Wilms' Tumor Study Group Pathology Center. Am J Surg Pathol 24 (2000) 4-18
34. Rakheja D., Weinberg A.G., Tomlinson G.E., Partridge K., and Schneider N.R. Translocation (10;17)(q22;p13): a recurrent translocation in clear cell sarcoma of kidney. Cancer Genet Cytogenet 154 (2004) 175-179
35. Bonnin J.M., Rubinstein L.J., Palmer N.F., and Beckwith J.B. The association of embryonal tumors originating in the kidney and in the brain. Cancer 54 (1984) 2137-2146
36. Weeks D.A., Beckwith J.B., Mierau G.W., and Luckey C.W. Rhabdoid tumor of kidney. A report of 111 cases from the National Wilms' Tumor Study Pathology Center. Am J Surg Pathol 13 (1989) 439-458
37. Vujanic G.M., Sandstedt B., Harms D., Bocon-Gibod L., and Delemare J.F. Rhabdoid tumour of the kidney: a clinicopathological study of 22 patients from the International Society of Paediatric Oncology (SIOP) nephroblastoma file. Histopathology 28 (1996) 333-340
38. Weeks D.A., Beckwith J.B., Mierau G.W., and Zuppan C.W. Renal neoplasms mimicking rhabdoid tumor of kidney. A report from the National Wilms' Tumor Study Pathology Center. Am J Surg Pathol 15 (1991) 1042-1054
39. Vertsteege I., Sevenet N., Lange J., et al. Truncating mutation of hSNF5/INI1 in aggressive paediatric cancer. Nature 394 (1998) 203-206
40. Hoot A.C., Rus P., Judkins A.R., Perlman E.J., and Biegel J.A. Immunohistochemical analysis of hSNF5/INI1 distinguishes renal and extra-renal malignant rhabdoid tumors from other pediatric soft tissue tumors. Am J Surg Pathol 28 (2004) 1485-1491
41. Tomplison G.E., Breslow N.E., Dome J., et al. Rhabdoid tumor of the kidney in the National Wilms' Tumor Group: age at diagnosis as a prognostic factor. J Clin Oncol 23 (2005) 7641-7645
42. Sotelo-Avila C., Beckwith J.B., and Johnson J.E. Ossifying renal tumor of infancy: a clinicopathologic study of nine cases. Pediatr Pathol 15 (1995) 745-762