Wilms tumor dataset: socio-demographic, clinicopathological, histological features and disease progression of 84 Moroccan infants

Published: 29 November 2023| Version 1 | DOI: 10.17632/zdhc7fyzr3.1


Wilms tumour (WT), also known as nephroblastoma, is a malignant kidney tumour that accounts for 5% of all paediatric cancers and 95% of childhood malignant renal neoplasms, with an incidence of 1 in 10,000 children. This clinical dataset provides information from 84 Moroccan patients diagnosed with Wilms tumor, and treated following the SIOP 2001 protocol. The key variables include demographic and epidemiological data (including gender, age, clinical history and comorbidities), clinical and paraclinical features (such as medical complaint, symptoms, tumor features, metastatic extensions, and anatomopathological findings), treatment regimen (involving nephrectomy, chemotherapy and x-ray treatment), clinical evaluation and patient prognosis (encompassing complete remission, relapse or mortality). The dataset can be used to relate clinical characteristics to tumor features and progression under therapy for risk stratification and better treatment management.



Centre National pour la Recherche Scientifique et Technique, Centre Hospitalo-Universitaire Ibn Sina, Universite Mohammed V de Rabat


Cancer, Wilms Tumor, Pediatric Cancer, Clinical Oncology, Morocco