@Article{Hajzler2021,
journal="Pediatria Polska - Polish Journal of Paediatrics",
issn="0031-3939",
volume="96",
number="2",
year="2021",
title="Characteristics of patients with blastemal-type Wilms’ tumour",
abstract="Wilms’ tumour (nephroblastoma) is the most common malignant tumour of kidney in children and one of the 2 most common solid tumours located outside of the central nervous system. Nephroblastoma has a very good prognosis, but some histological types like blastemal-type require qualification to a high-risk group and intensification of treatment. We present the cases of 3 children diagnosed with nephroblastoma, blastemal-type. The first girl’s treatment was unsuccessful, as there were 4 cancer recurrences. The second girl had primarily metachronous form of nephroblastoma, but during recurrence the blastemal-type was diagnosed. Despite intensive treatment, it ended with failure. The third girl had a tumour in the left kidney, which was transformed from the bilateral nephroblastomatosis. She remains in remission; the therapy ended on February 2018.",
author="Hajzler, Weronika
and Kopera, Joanna
and Kosek, Klaudia
and Mazur, Dorota
and Rurańska, Iwona
and Szczepański, Tomasz
and Pobudejska-Pieniążek, Aneta",
pages="134--138",
doi="10.5114/polp.2021.107397",
url="http://dx.doi.org/10.5114/polp.2021.107397"
}