Description of Nephroblastoma Cases Diagnosed in a Laboratory of Pathology located at Sao Paulo City, Brazil

Authors

  • Marcela Silva Menezes Universidade Nove de Julho (UNINOVE). São Paulo (SP), Brasil.
  • Fabio Daniel Molinari Hospital Israelita Albert Einstein. São Paulo (SP), Brasil.
  • João Victor Fornari Universidade Federal de São Paulo (UNIFESP). São Paulo (SP), Brasil. Universidade Nove de Julho (UNINOVE). São Paulo (SP), Brasil.
  • Anderson Sena Barnabé Universidade de São Paulo(USP). São Paulo(SP), Brasil. Universidade Nove de Julho (UNINOVE). São Paulo (SP), Brasil.
  • Samanta Cordeiro Silva Universidade Gama Filho. São Paulo (SP), Brasil.
  • Amanda Lima Bezerra Faculdades Metropolitanas Unidas (FMU). São Paulo (SP), Brasil.
  • Roberto El Ibrahim Sociedade Brasileira de Patologia. São Paulo (SP), Brasil.
  • Renato Ribeiro Nogueira Ferraz Universidade Federal de São Paulo (UNIFESP). São Paulo (SP), Brasil. Universidade Nove de Julho (UNINOVE). São Paulo (SP), Brasil.

DOI:

https://doi.org/10.32635/2176-9745.RBC.2013v59n2.518

Keywords:

Kidney Neoplasms, Wilms Tunor, Wilms Tunor-diagnosis, Wilms Tunor-pathology, Child

Abstract

Introduction: Renal cancer corresponds to 2% of the malignant tumors in human beings. Amongst the highest incidence renal tumors, the nephroblastoma, also known as the Wilms’ tumor, is the most common malignant neoplasm in children. Objective: Describe 15 cases of nephroblastoma (Wilms' tumor) diagnosed at a laboratory specializing in Anatomic Pathology, located in the central region of São Paulo city, from April 2003 to August 2011. Method: A descriptive, retrospective study, which evaluated medical records of patients who underwent diagnostic tests for kidney disease. Medical appraisal survey of renal samples obtained through nephrectomy or biopsy, macroscopical and microscopical anatomopathologic diagnosis, age and gender of the involved individuals, striving to define the Wilms’ tumor bearer population. Results: Among 2,277 patients samples, 15 were diagnosed positive for nephroblastoma (Wilms’ tumor), being the highest rates (67% f the cases) on male individuals. In 47% of the cases, the tumor was classified as stage I. Conclusion: Knowing the population usually affected by nephroblastoma may contribute to early diagnosis and thereby improve the prognosis of the affected individuals.

 

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Published

2013-06-28

How to Cite

1.
Menezes MS, Molinari FD, Fornari JV, Barnabé AS, Silva SC, Bezerra AL, Ibrahim RE, Ferraz RRN. Description of Nephroblastoma Cases Diagnosed in a Laboratory of Pathology located at Sao Paulo City, Brazil. Rev. Bras. Cancerol. [Internet]. 2013 Jun. 28 [cited 2024 Jul. 22];59(2):185-91. Available from: https://rbc.inca.gov.br/index.php/revista/article/view/518

Issue

Section

ORIGINAL ARTICLE