CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2012; 33(02): 102-106
DOI: 10.4103/0971-5851.99744
ORIGINAL ARTICLE

Study of histopathological features and proliferation markers in cases of Wilms′ tumor

Ram Narayan Das
Department of Pathology, I.P.G.M.E and R, Kolkata, West Bengal, India
,
Uttara Chatterjee
Department of Pathology, I.P.G.M.E and R, Kolkata, West Bengal, India
,
Swapan K Sinha
Department of Pathology, I.P.G.M.E and R, Kolkata, West Bengal, India
,
Ashoke K Ray
Department of Pediatric Surgery, I.P.G.M.E and R, Kolkata, West Bengal, India
,
Koushik Saha
N.R.S.M.C and H, Kolkata, West Bengal, India
,
Sugato Banerjee
Paediatric Surgeon of Park Children Centre for Treatment and Research, KPC Medical College, Kolkata, West Bengal, India
› Author Affiliations

Abstract

Context: The spectrum of pediatric renal tumors is different from adult renal tumors, and Wilms′ tumor (WT) forms the majority. The histological type and clinicopathological staging are the two important prognostic parameters. The role of newer prognostic factors is not clear. Aims: This study was performed to analyze the histopathological spectrum of pediatric renal tumors and to study the expression of proliferation markers (Ki-67 and p53) in WT and correlate its expression in epithelial and blastema components in different stages. Materials and Methods: Twenty-seven cases of pediatric renal tumors were collected over 2 years. Hematoxylin-eosin staining was used for diagnosis. Immunostaining was performed for Ki-67 and p53. Ki-67 proliferation index (PI) and p53 expression were determined in each case and for the epithelial and blastema components separately. Statistical Analysis and Results: We had 20 cases of WT (74.1%), three cases of mesoblastic nephroma (11.1%), three cases of clear cell sarcoma (11.1%) and one case of rhabdoid tumor (3.7%). It was observed that the PI of the epithelial component (57.2%) was significantly higher than that of blastema (39.53%) in all stages. The PI in Stage II is significantly higher than that in Stage I. Statistical analysis could not be performed in Stages III and IV due to the small number of cases. p53 expression did not show any significant difference in the epithelial and blastema components. There was also no significant difference between the stages. Conclusion: In this study, we found the differences between PI of different tissue components of WT, with the epithelial component having a higher PI, which correlated with the stage of advancement of the disease.



Publication History

Article published online:
13 April 2022

© 2012. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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  • References

  • 1 Argani P, Beciwith JB. Renal Neoplasm of Childhood. In: Mills SE, editor. Sternberg′s Diagnostic Surgical Pathology. 14 th ed. Philadelphia: Lippincott Williams and Wilkins: 2004. p. 2005-16.
  • 2 Jaffe N, Huff V. Neoplasm of the kidney. In: Behrman RE, Kliegmen RM, Jenson HB, editors. Nelson′s Text book of Pediatrics. 17 th ed. Philadelphia: Saunders Elsevier; 2004. p. 1711-4.
  • 3 Ordonez NG, Rosai J. Urinary tract. In: Rosai J, editor. Rosai and Ackerman′s Surgical Pathology. 9 th ed. St. Louis: Mosby, Elsevier; 2004. p. 1240-5.
  • 4 Beckwith JB. Wilms′ tumor and other renal tumors of childhood. A selective review from the National Wilms′ study pathology center. Hum Pathol 1983;14:481-92.
  • 5 Mishra K, Mathur M, Kakkar N. Precursor Lesions of Wilms′ Tumor in Indian Children. Cancer 1998;83:2228-32.
  • 6 Gutjahr P, Kaatsch P, Spaar HJ, Neithammer D, Gobel G, Henze G, et al. Therapie und Prognose bei 373 Kindern mit Wilms- Tumoren-Ergebnisse der bundesweiten Studie 1980- 88. Akt Urol 1990;21:132-41.
  • 7 Ghanem MA, Van der Kwasth TH, Sudaryo MK, Mathoera RB, van den Heuvel MM, Al-Doray AA, et al. MIB1 proliferation index and cyclin dependent kinase inhibitor p27 protein expression in nephroblastoma. Clin Cancer Res 2004:10;591-7.
  • 8 Beniers AJ, Efferth T, Fuzesi L, Granzen B, Mertens R, Janse G. p53 expression in WT: Apossible role as prognostic factor. Int J Oncol 2001;18:133-9.
  • 9 Faria P, Beckwith JB, Mishra K, Zuppan C, Weeks DA, Breslow N, et al. Focal versus diffuse anaplasia in WT: New definition with prognostic significance: A report from the NWTSG. Am J Surg Pathol 1996;20:909-20.
  • 10 Khine MM, Aung W, Sibbons PD, Howard CV, Clapham E, McGill F, et al. Analysis of relative proliferation rates of Wilms′ tumor components using proliferating cell nuclear antigen and MIB-1 (Ki-67 equivalent antigen) immunostaining and assessment of mitotic index. Lab Invest 1994;70:125-9.
  • 11 Juszkiewicz P, Tuziak T, Zbislawski W, Leibhard M, Chosia M. Tumor cell proliferation rate as determined by MIB-1 antibody in WT. Pol J Pathol 1997;48:113-9.
  • 12 Skotnicka - Klonowicz G, Kobos J, Los E, Trejster E, Szymik - Kantorowicz S, Daszkiewicz P. Prognostic Value of proliferating cell nuclear antigen in WT in children. Eur J Surg Oncl 2002;28:67-71.
  • 13 Sredni ST, de Camargo B, Lopes LF, Teixeira R, Simpson A. Immunohistochemical detection of p53 protein expression as a prognostic indicator in Wilms tumor. Med Pediator Oncol 2001;37:455-8.
  • 14 Huang J, Soffer SZ, Kim ES, Yokoi A, Moore JT, Mc Crudden KW, et al. p53 accumulation in favourable histology WT is associated with angiogenesis and clinically aggressive disease. J Pediatr Surg 2002;37:523-7.
  • 15 Malkin D, Sexsmith E, Yeger H, Williams BR. Mutations of p53 tumor suppressor gene occur infrequently in WT. Cancer Res 1993;54:2077-9.
  • 16 Lahoti C, Thorner P, Malkin D, Yeger H. Immunohistochemical detection of p53 in Wilms′ tumors correlates with unfavourable outcome. Am J Pathol 1996;148:1577-89.