نتایج جستجو برای: intravascular extension of wilms tumor

تعداد نتایج: 21220822  

2016
Prince Raj Ashwini Khanolkar Yogesh Kumar Sarin

Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms' tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms' tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metaneph...

Journal: :Cancer research 1988
N Breslow J B Beckwith M Ciol K Sharples

Median ages at diagnosis were 36.5 and 42.5 mo for 1523 males and 1678 females with unilateral Wilms' tumor registered between October 1969 and December 1985; they were 23.5 mo and 30.5 mo for 100 males and 141 females with bilateral disease. The median age for multicentric, unilateral cases was intermediate between the bilateral and unicentric medians. Patients with hemihypertrophy in addition...

Journal: :Urologia internationalis 2009
T Maurer C Zorn E Klein G Weirich A J Beer J E Gschwend N Zantl

Wilms tumor, or nephroblastoma, is the most common malignant tumor of the urinary tract in children, but is rarely found in adults. Here, we report the first case of a female patient with a Wilms tumor, diagnosed during pregnancy, who underwent radical nephrectomy and adjuvant chemotherapy before and after delivering a healthy child. Generally, treatment should follow the guidelines established...

2005
Wenliang Li Patricia Kessler Herman Yeger Jennifer Alami Anthony E. Reeve Rosemary Heathcott Jane Skeen

Anaplastic histology and metastasis are each associated with higher relapse and mortality rates in Wilms tumor patients. However, not all anaplastic tumors relapse and some nonanaplastic tumors relapse unexpectedly. To identify more accurate early prognostic indicators, we analyzed expression of 4,900 cancer-related genes in 26 primary Wilms tumors. This analysis revealed that expression of a s...

Journal: :Cancer research 2005
Wenliang Li Patricia Kessler Herman Yeger Jennifer Alami Anthony E Reeve Rosemary Heathcott Jane Skeen Bryan R G Williams

Anaplastic histology and metastasis are each associated with higher relapse and mortality rates in Wilms tumor patients. However, not all anaplastic tumors relapse and some nonanaplastic tumors relapse unexpectedly. To identify more accurate early prognostic indicators, we analyzed expression of 4,900 cancer-related genes in 26 primary Wilms tumors. This analysis revealed that expression of a s...

Journal: :Medical and pediatric oncology 2003
Herwig Lackner Christian Urban Hans Jürgen Dornbusch Wolfgang Schwinger Reinhold Kerbl Petra Sovinz

1. Webber BL, Parham DM, Drake LG, et al. Renal tumors in childhood. Pathol Ann Part 1992;1:191–232. 2. Murphy WM, Beckwith JB, Farrow GM. Tumors of the kidney, bladder and related urinary structures. In: Murphy WM, Beckwith JB, Farrow GM, editors. Atlas of tumor pathology, series 3, fascicle 11. Washington D.C.: Armed Forces Institute of Pathology, 1994. 3. Beckwith JB. Pediatric neoplastic di...

Journal: :Neurologia medico-chirurgica 1991

Journal: :Indian Journal of Medical and Paediatric Oncology 2020

Journal: :Sao Paulo medical journal = Revista paulista de medicina 2000
R Defavery J A Lemos S Kashima J E Bernardes C A Scridelli D T Covas L G Tone

CONTEXT Mutations of the p53 tumor suppressor gene are the most frequent alterations observed in human neoplasias affecting adults. In pediatric oncology, however, they have seldom been identified. Wilms' tumor is a renal neoplasia commonly occurring in children and is associated with mutations of the WT1 gene. The correlation between Wilms' tumor and alterations of the p53 gene has not been we...

Journal: :International braz j urol : official journal of the Brazilian Society of Urology 2007
Silvio Tucci Adauto J Cologna Haylton J Suaid Elvis T Valera Luis F Tirapelli Edson L Paschoalin Antonio C Martins

OBJECTIVE To evaluate treatment outcomes in Wilms' tumor (WT). MATERIALS AND METHODS We studied 53 children with median age of 2 years with WT, stages I-19, II-14, III-12, IV-6 and V-2. Treatment consisted of surgical excision plus adjuvant (40 children) or neoadjuvant and adjuvant chemotherapy (unresectable tumor, n=8, or caval tumor extension, n=5). Chemotherapy and radiotherapy followed pr...

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