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Year 2006, Volume: 4 Issue: 1, 128 - 132, 01.04.2006

Abstract

References

  • 1. Gurney JG, Davis S, Severson RK, Fang JY, Ross JA, Robison LL. Trends in cancer incidence among children in the U.S. Cancer 1996; 78:532-41.
  • 2. Gurney JG, Ross JA, Wall DA, Bleyer WA, Severson RK, Robison LL. Infant cancer in the U.S.: histology-specific incidence and trends, 1973 to 1992. J Pediatr Hematol Oncol 1997; 19:428-32.
  • 3. Olshan AF, Smith J, Cook MN, et al. Hormone and fertility drug use and the risk of neuroblastoma: a report from the Children's Cancer Group and the Pediatric Oncology Group. Am J Epidemiol 1999; 150:930-8.
  • 4. Olshan AF, De Roos AJ, Teschke K, et al. Neuroblastoma and parental occupation. Cancer Causes Control 1999; 10:539-49.
  • 5. Knudson AG Jr, Strong LC. Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet 1972; 24:514-32.
  • 6. Maris JM, Weiss MJ, Mosse Y, et al. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res 2002; 62:6651-8.
  • 7. Kushner BH, Gilbert F, Helson L. Familial neuroblastoma. Case reports, literature review, and etiologic considerations. Cancer 1986; 57(9):1887- 93.
  • 8. Verloes A, Elmer C, Lacombe D, et al. Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature. Eur J Pediatr 1993; 152:75-7.
  • 9. Maris JM, Weiss MJ, Mosse Y, et al. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res 2002; 62:6651-8.
  • 10. Seeger RC, Brodeur GM, Sather H, et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 1985; 313:1111-6.
  • 11. Brodeur GM, Maris JM. Neuroblastoma. In: Pizzo PA, Poplack DG (eds). Principles and Practice of Pediatric Oncology. 4th edition. Lippincott Williams & Wilkins; 2001:933-70.
  • 12. Caron H. Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma. Med Pediatr Oncol 1995; 24:215-21.
  • 13. Gehring M, Berthold F, Edler L, Schwab M, Amler LC. The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma. Cancer Res 1995; 55:5366-9.
  • 14. Martinsson T, Sjoberg RM, Hedborg F, Kogner P. Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms. Cancer Res 1995; 55:5681-6.
  • 15. White PS, Thompson PM, Gotoh T, et al. Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma. Oncogene 2005; 24:2684-94.
  • 16. Caron H, van Sluis P, de Kraker J, et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med 1996; 334:225-30.
  • 17. Maris JM, Weiss MJ, Guo C, et al. Loss of heterozygosity at 1p36 independently predicts for disease progression but not decreased overall survival probability in neuroblastoma patients: a Children's Cancer Group study. J Clin Oncol 2000; 18(9):1888-99.
  • 18. Spitz R, Hero B, Ernestus K, Berthold F. Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma. Clin Cancer Res 2003; 9:52-8.
  • 19. Yano H, Chao MV. Neurotrophin receptor structure and interactions. Pharm Acta Helv. 2000; 74:253-60.
  • 20. Patapoutian A, Reichardt LF. Trk receptors: mediators of neurotrophin action. Curr Opin Neurobiol 2001; 11:272-80.
  • 21. Nakagawara A, Arima-Nakagawara M, Scavarda NJ, Azar CG, Cantor AB, Brodeur GM. Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma. N Engl J Med 1993; 328:847-54.
  • 22. Nakagawara A, Azar CG, Scavarda NJ, Brodeur GM. Expression and function of TRK-B and BDNF in human neuroblastomas. Mol Cell Biol 1994; 14:759-67.
  • 23. Brodeur GM. Neuroblastoma:biological insights into a clinical enigma. Nat Rev Cancer 2003; 3:203-16.
  • 24. Yamada S, Ishii E, Nakagawara A, et al. Features and outcome of advanced neuroblastoma with distant lymph node metastasis. Pediatr Hematol Oncol 1992; 9:49-56.
  • 25. DuBois SG, Kalika Y, Lukens JN, et al. Metastatic sites in stage IV and IVS neuroblastoma correlate with age, tumor biology, and survival. J Pediatr Hematol Oncol 1999; 21:181-9.
  • 26. Ho PT, Estroff JA, Kozakewich H, et al. Prenatal detection of neuroblastoma: a ten-year experience from the Dana-Farber Cancer Institute and Children's Hospital. Pediatrics 1993; 92:358-64.
  • 27. Monsaingeon M, Perel Y, Simonnet G, Corcuff JB. Comparative values of catecholamines and metabolites for the diagnosis of neuroblastoma. Eur J Pediatr 2003; 162:397-402.
  • 28. Kaplan SJ, Holbrook CT, McDaniel HG, Buntain WL, Crist WM. Vasoactive intestinal peptide secreting tumors of childhood. Am J Dis Child 1980; 134:21-4.
  • 29. Qualman SJ, O'Dorisio MS, Fleshman DJ, Shimada H, O'Dorisio TM. Neuroblastoma. Correlation of neuropeptide expression in tumor tissue with other prognostic factors. Cancer 1992; 70:2005-12.
  • 30. Rudnick E, Khakoo Y, Antunes NL, et al. Opsoclonus-myoclonus-ataxia syndrome in neuroblastoma: clinical outcome and antineuronal antibodies-a report from the Children's Cancer Group Study. Med Pediatr Oncol 2001; 36:612-22.
  • 31. Pranzatelli MR, Travelstead AL, Tate ED, et al. B- and T-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes. Neurology 2004; 62:1526-32.
  • 32. Brodeur GM, Seeger RC, Barrett A, et al. International criteria for diagnosis, staging, and response to treatment in patients with neuroblastoma. J Clin Oncol 1988; 6:1874-81.
  • 33. Brodeur GM, Pritchard J, Berthold F, et al. Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 1993; 11:1466-77.
  • 34. Gatta G, Capocaccia R, Stiller C, Kaatsch P, Berrino F, Terenziani M; EUROCARE Working Group. Childhood cancer survival trends in Europe: a EUROCARE Working Group study. J Clin Oncol 2005; 23:3742-51.
  • 35. Sawada T, Kidowaki T, Sakamoto I, et al. Neuroblastoma. Mass screening for early detection and its prognosis. Cancer 1984; 53:2731-5.
  • 36. Takeda T, Hatae Y, Nakadate H, et al. Japanese experience of screening. Med Pediatr Oncol 1989; 17:368-72.
  • 37. Woods WG, Tuchman M, Robison LL, et al. A population-based study of the usefulness of screening for neuroblastoma. Lancet 1996; 348:1682-7.
  • 38. Schilling FH, Berthold F, Erttmann R, et al. Population-based and controlled study to evaluate neuroblastoma screening at one year of age in Germany: interim results. Med Pediatr Oncol 2000; 35:701-4.
  • 39. Bessho F. Comparison of the incidences of neuroblastoma for screened and unscreened cohorts. Acta Paediatr 1999; 88:404-6.
  • 40. Yamamoto K, Ohta S, Ito E, et al. Marginal decrease in mortality and marked increase in incidence as a result of neuroblastoma screening at 6 months of age: cohort study in seven prefectures in Japan. J Clin Oncol 2002; 20:1209-14.
  • 41. Woods WG, Gao RN, Shuster JJ, et al. Screening of infants and mortality due to neuroblastoma. N Engl J Med 2002; 346:1041-6.

Nöroblastom

Year 2006, Volume: 4 Issue: 1, 128 - 132, 01.04.2006

Abstract

Nöroblastom; adrenal medulla ve sempatik ganglionlarda görülen ve ilkel nöral krest hücrelerinden orijin alan bir tümördür. Diğer tümörlerle karşılaştırıldığında; primer tümörün, metastatik hastalığın ve paraneoplastik sendromların farklı klinik presentasyonu olabilir. Spontan regresyonlar, benign hastalı- ğa farklılaşma, ileri yaştaki çocuklarda oldukça malign seyretmesi, nöroblastomun farklı davranışlarına örnek olarak verilebilir.

References

  • 1. Gurney JG, Davis S, Severson RK, Fang JY, Ross JA, Robison LL. Trends in cancer incidence among children in the U.S. Cancer 1996; 78:532-41.
  • 2. Gurney JG, Ross JA, Wall DA, Bleyer WA, Severson RK, Robison LL. Infant cancer in the U.S.: histology-specific incidence and trends, 1973 to 1992. J Pediatr Hematol Oncol 1997; 19:428-32.
  • 3. Olshan AF, Smith J, Cook MN, et al. Hormone and fertility drug use and the risk of neuroblastoma: a report from the Children's Cancer Group and the Pediatric Oncology Group. Am J Epidemiol 1999; 150:930-8.
  • 4. Olshan AF, De Roos AJ, Teschke K, et al. Neuroblastoma and parental occupation. Cancer Causes Control 1999; 10:539-49.
  • 5. Knudson AG Jr, Strong LC. Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet 1972; 24:514-32.
  • 6. Maris JM, Weiss MJ, Mosse Y, et al. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res 2002; 62:6651-8.
  • 7. Kushner BH, Gilbert F, Helson L. Familial neuroblastoma. Case reports, literature review, and etiologic considerations. Cancer 1986; 57(9):1887- 93.
  • 8. Verloes A, Elmer C, Lacombe D, et al. Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature. Eur J Pediatr 1993; 152:75-7.
  • 9. Maris JM, Weiss MJ, Mosse Y, et al. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res 2002; 62:6651-8.
  • 10. Seeger RC, Brodeur GM, Sather H, et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 1985; 313:1111-6.
  • 11. Brodeur GM, Maris JM. Neuroblastoma. In: Pizzo PA, Poplack DG (eds). Principles and Practice of Pediatric Oncology. 4th edition. Lippincott Williams & Wilkins; 2001:933-70.
  • 12. Caron H. Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma. Med Pediatr Oncol 1995; 24:215-21.
  • 13. Gehring M, Berthold F, Edler L, Schwab M, Amler LC. The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma. Cancer Res 1995; 55:5366-9.
  • 14. Martinsson T, Sjoberg RM, Hedborg F, Kogner P. Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms. Cancer Res 1995; 55:5681-6.
  • 15. White PS, Thompson PM, Gotoh T, et al. Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma. Oncogene 2005; 24:2684-94.
  • 16. Caron H, van Sluis P, de Kraker J, et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med 1996; 334:225-30.
  • 17. Maris JM, Weiss MJ, Guo C, et al. Loss of heterozygosity at 1p36 independently predicts for disease progression but not decreased overall survival probability in neuroblastoma patients: a Children's Cancer Group study. J Clin Oncol 2000; 18(9):1888-99.
  • 18. Spitz R, Hero B, Ernestus K, Berthold F. Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma. Clin Cancer Res 2003; 9:52-8.
  • 19. Yano H, Chao MV. Neurotrophin receptor structure and interactions. Pharm Acta Helv. 2000; 74:253-60.
  • 20. Patapoutian A, Reichardt LF. Trk receptors: mediators of neurotrophin action. Curr Opin Neurobiol 2001; 11:272-80.
  • 21. Nakagawara A, Arima-Nakagawara M, Scavarda NJ, Azar CG, Cantor AB, Brodeur GM. Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma. N Engl J Med 1993; 328:847-54.
  • 22. Nakagawara A, Azar CG, Scavarda NJ, Brodeur GM. Expression and function of TRK-B and BDNF in human neuroblastomas. Mol Cell Biol 1994; 14:759-67.
  • 23. Brodeur GM. Neuroblastoma:biological insights into a clinical enigma. Nat Rev Cancer 2003; 3:203-16.
  • 24. Yamada S, Ishii E, Nakagawara A, et al. Features and outcome of advanced neuroblastoma with distant lymph node metastasis. Pediatr Hematol Oncol 1992; 9:49-56.
  • 25. DuBois SG, Kalika Y, Lukens JN, et al. Metastatic sites in stage IV and IVS neuroblastoma correlate with age, tumor biology, and survival. J Pediatr Hematol Oncol 1999; 21:181-9.
  • 26. Ho PT, Estroff JA, Kozakewich H, et al. Prenatal detection of neuroblastoma: a ten-year experience from the Dana-Farber Cancer Institute and Children's Hospital. Pediatrics 1993; 92:358-64.
  • 27. Monsaingeon M, Perel Y, Simonnet G, Corcuff JB. Comparative values of catecholamines and metabolites for the diagnosis of neuroblastoma. Eur J Pediatr 2003; 162:397-402.
  • 28. Kaplan SJ, Holbrook CT, McDaniel HG, Buntain WL, Crist WM. Vasoactive intestinal peptide secreting tumors of childhood. Am J Dis Child 1980; 134:21-4.
  • 29. Qualman SJ, O'Dorisio MS, Fleshman DJ, Shimada H, O'Dorisio TM. Neuroblastoma. Correlation of neuropeptide expression in tumor tissue with other prognostic factors. Cancer 1992; 70:2005-12.
  • 30. Rudnick E, Khakoo Y, Antunes NL, et al. Opsoclonus-myoclonus-ataxia syndrome in neuroblastoma: clinical outcome and antineuronal antibodies-a report from the Children's Cancer Group Study. Med Pediatr Oncol 2001; 36:612-22.
  • 31. Pranzatelli MR, Travelstead AL, Tate ED, et al. B- and T-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes. Neurology 2004; 62:1526-32.
  • 32. Brodeur GM, Seeger RC, Barrett A, et al. International criteria for diagnosis, staging, and response to treatment in patients with neuroblastoma. J Clin Oncol 1988; 6:1874-81.
  • 33. Brodeur GM, Pritchard J, Berthold F, et al. Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 1993; 11:1466-77.
  • 34. Gatta G, Capocaccia R, Stiller C, Kaatsch P, Berrino F, Terenziani M; EUROCARE Working Group. Childhood cancer survival trends in Europe: a EUROCARE Working Group study. J Clin Oncol 2005; 23:3742-51.
  • 35. Sawada T, Kidowaki T, Sakamoto I, et al. Neuroblastoma. Mass screening for early detection and its prognosis. Cancer 1984; 53:2731-5.
  • 36. Takeda T, Hatae Y, Nakadate H, et al. Japanese experience of screening. Med Pediatr Oncol 1989; 17:368-72.
  • 37. Woods WG, Tuchman M, Robison LL, et al. A population-based study of the usefulness of screening for neuroblastoma. Lancet 1996; 348:1682-7.
  • 38. Schilling FH, Berthold F, Erttmann R, et al. Population-based and controlled study to evaluate neuroblastoma screening at one year of age in Germany: interim results. Med Pediatr Oncol 2000; 35:701-4.
  • 39. Bessho F. Comparison of the incidences of neuroblastoma for screened and unscreened cohorts. Acta Paediatr 1999; 88:404-6.
  • 40. Yamamoto K, Ohta S, Ito E, et al. Marginal decrease in mortality and marked increase in incidence as a result of neuroblastoma screening at 6 months of age: cohort study in seven prefectures in Japan. J Clin Oncol 2002; 20:1209-14.
  • 41. Woods WG, Gao RN, Shuster JJ, et al. Screening of infants and mortality due to neuroblastoma. N Engl J Med 2002; 346:1041-6.
There are 41 citations in total.

Details

Primary Language Turkish
Journal Section Collection
Authors

Metin Demirkaya This is me

Betül Sevinir This is me

Publication Date April 1, 2006
Published in Issue Year 2006 Volume: 4 Issue: 1

Cite

APA Demirkaya, M., & Sevinir, B. (2006). Nöroblastom. Güncel Pediatri, 4(1), 128-132.
AMA Demirkaya M, Sevinir B. Nöroblastom. Güncel Pediatri. April 2006;4(1):128-132.
Chicago Demirkaya, Metin, and Betül Sevinir. “Nöroblastom”. Güncel Pediatri 4, no. 1 (April 2006): 128-32.
EndNote Demirkaya M, Sevinir B (April 1, 2006) Nöroblastom. Güncel Pediatri 4 1 128–132.
IEEE M. Demirkaya and B. Sevinir, “Nöroblastom”, Güncel Pediatri, vol. 4, no. 1, pp. 128–132, 2006.
ISNAD Demirkaya, Metin - Sevinir, Betül. “Nöroblastom”. Güncel Pediatri 4/1 (April 2006), 128-132.
JAMA Demirkaya M, Sevinir B. Nöroblastom. Güncel Pediatri. 2006;4:128–132.
MLA Demirkaya, Metin and Betül Sevinir. “Nöroblastom”. Güncel Pediatri, vol. 4, no. 1, 2006, pp. 128-32.
Vancouver Demirkaya M, Sevinir B. Nöroblastom. Güncel Pediatri. 2006;4(1):128-32.