Volume 56, Issue 4 pp. 534-540
Original Article

Wilms tumor: Experience of a hospital in southern Brazil

Valentina Oliveira Provenzi

Valentina Oliveira Provenzi

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Rafael Fabiano Machado Rosa

Rafael Fabiano Machado Rosa

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Rosana Cardoso Manique Rosa

Rosana Cardoso Manique Rosa

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Adriana Vial Roehe

Adriana Vial Roehe

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Pedro Paulo Albino dos Santos

Pedro Paulo Albino dos Santos

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Fabrízia Rennó Sodero Faulhaber

Fabrízia Rennó Sodero Faulhaber

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Ceres Andréia Vieira de Oliveira

Ceres Andréia Vieira de Oliveira

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

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Paulo Ricardo Gazzola Zen

Corresponding Author

Paulo Ricardo Gazzola Zen

Conceição Hospital Group and Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil

Correspondence: Paulo Ricardo Gazzola Zen, MD PhD, Genética Clínica–UFCSPA/CHSCPA, Rua Sarmento Leite, 245/403, 90050-170 Porto Alegre, Brazil. Email: [email protected]Search for more papers by this author
First published: 21 January 2014
Citations: 9

Abstract

Background

Wilms tumor (WT) is the most common renal malignancy of childhood. The aim of this study was to verify the epidemiological profile and prognosis of a sample of patients from Brazil and compare them to similar data from other Latin American studies.

Method

The sample consisted of consecutive patients diagnosed with WT in an oncohematology service of a referral hospital in Southern Brazil, between 1989 and 2009. Clinical, radiological, pathological and survival data were collected from the medical records. Analysis was done using Excel and SPSS version 18.0. The significance level was set at P < 0.05.

Results

The final sample consisted of 45 patients. The male/female ratio was 1.25:1. Mean age at diagnosis was 43.9 months and all patients were of European descent. Thirty-three patients (73.3%) had both signs/symptoms of abdominal mass and hypertension. Malformation was observed in nine patients (20%) and there was one case of Fanconi's anemia (2.2%). Three patients had bilateral disease (6.7%). The majority of patients had stage III and IV (62.2%). Patients with malformation had an earlier age at diagnosis (P = 0.018) and a higher prevalence of bilateral disease (P = 0.044). Overall survival was 75%. Age at diagnosis was the only significant independent predictor associated with death.

Conclusion

Death is closely related to late diagnosis in WT. Oncologic services should also be concerned about morbidity caused by therapeutic options in cases of late diagnosis, and the consequences for quality of life.

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