Wilms tumour: fifteen years experience of a single institution

Paraskevi Panagopoulou; Vasiliki Fragandrea-Sidi; Ioanna Fragandrea; Eleftherios Smaropoulos; Eirini Kazantzidou; Dimitrios Koliouskas

doi:10.1002/pbc.22779

Wilms tumour: fifteen years experience of a single institution

Paraskevi Panagopoulou, Vasiliki Fragandrea-Sidi, Ioanna Fragandrea, Eleftherios Smaropoulos, Eirini Kazantzidou, Dimitrios Koliouskas

Management Science

Research output: Contribution to journal › Conference abstract › peer-review

Abstract

Purpose: to investigate the incidence, clinicopathological features, treatment and survival of patients with Wilms Tumor (WT) during a 15-year period in a Paediatric Oncology Department of a tertiary hospital. Method: All children with WT were identified among 786 patients treated in our department between January 1, 1993 and December 31, 2008. Patient files were reviewed and the following data were recorded: gender, age at diagnosis, clinical presentation, pathology reports, treatment, follow-up and outcome. Results: A total of 56 patients (27 male) were identified. Male:female ratio was 1:1, age range: 8 months–12 years whereas 75% were

Original language	English
Pages (from-to)	885
Number of pages	1
Journal	Pediatric Blood and Cancer
Volume	55
Issue number	5
DOIs	https://doi.org/10.1002/pbc.22779
Publication status	Published - 30 Nov 2010
Event	42nd Congress of the International Society of Paediatric Oncology - Boston, United States Duration: 21 Oct 2010 → 24 Oct 2010

Keywords

Wilms tumour
paediatric oncology

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10.1002/pbc.22779

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title = "Wilms tumour: fifteen years experience of a single institution",

abstract = "Purpose: to investigate the incidence, clinicopathological features, treatment and survival of patients with Wilms Tumor (WT) during a 15-year period in a Paediatric Oncology Department of a tertiary hospital. Method: All children with WT were identified among 786 patients treated in our department between January 1, 1993 and December 31, 2008. Patient files were reviewed and the following data were recorded: gender, age at diagnosis, clinical presentation, pathology reports, treatment, follow-up and outcome. Results: A total of 56 patients (27 male) were identified. Male:female ratio was 1:1, age range: 8 months–12 years whereas 75% were ",

keywords = "Wilms tumour, paediatric oncology",

author = "Paraskevi Panagopoulou and Vasiliki Fragandrea-Sidi and Ioanna Fragandrea and Eleftherios Smaropoulos and Eirini Kazantzidou and Dimitrios Koliouskas",

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TY - JOUR

T1 - Wilms tumour

T2 - 42nd Congress of the International Society of Paediatric Oncology

AU - Panagopoulou, Paraskevi

AU - Fragandrea-Sidi, Vasiliki

AU - Fragandrea, Ioanna

AU - Smaropoulos, Eleftherios

AU - Kazantzidou, Eirini

AU - Koliouskas, Dimitrios

PY - 2010/11/30

Y1 - 2010/11/30

N2 - Purpose: to investigate the incidence, clinicopathological features, treatment and survival of patients with Wilms Tumor (WT) during a 15-year period in a Paediatric Oncology Department of a tertiary hospital. Method: All children with WT were identified among 786 patients treated in our department between January 1, 1993 and December 31, 2008. Patient files were reviewed and the following data were recorded: gender, age at diagnosis, clinical presentation, pathology reports, treatment, follow-up and outcome. Results: A total of 56 patients (27 male) were identified. Male:female ratio was 1:1, age range: 8 months–12 years whereas 75% were

AB - Purpose: to investigate the incidence, clinicopathological features, treatment and survival of patients with Wilms Tumor (WT) during a 15-year period in a Paediatric Oncology Department of a tertiary hospital. Method: All children with WT were identified among 786 patients treated in our department between January 1, 1993 and December 31, 2008. Patient files were reviewed and the following data were recorded: gender, age at diagnosis, clinical presentation, pathology reports, treatment, follow-up and outcome. Results: A total of 56 patients (27 male) were identified. Male:female ratio was 1:1, age range: 8 months–12 years whereas 75% were

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KW - paediatric oncology

U2 - 10.1002/pbc.22779

DO - 10.1002/pbc.22779

M3 - Conference abstract

SN - 1545-5009

VL - 55

SP - 885

JO - Pediatric Blood and Cancer

JF - Pediatric Blood and Cancer

IS - 5

Y2 - 21 October 2010 through 24 October 2010

ER -

Wilms tumour: fifteen years experience of a single institution

Abstract

Keywords

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