نتایج جستجو برای: bilateral wilms

تعداد نتایج: 85842  

Journal: :iranian journal of pathology 2006
seyed mohammad bagher akhavirad ali davati mohammad reza jalali nadoushan mehdi abedini

background and objective: wilms’ tumor has been recognized as the most common primary malignancy of kidney at childhood, comprises 5-6% of tumors in this period, and manifests itself with various clinical symptoms. since there have been no sufficient studies in this field in iran, therefore, this study was conducted to investigate its histopathology and clinical symptoms. materials and methods:...

2013
Joanna Huszno Danuta Starzyczny–Słota Magdalena Jaworska Elżbieta Nowara

INTRODUCTION Wilms' tumour is one of the commonest malignant tumours of childhood. It appears mainly in the first 5 years of life. Incidental examples of nephroblastoma in adults have been described in literature (about 3% of all described cases). There are diagnostic and therapeutic difficulties in that older age group. The preoperative diagnosis of nephroblastoma in adults is difficult becaus...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2009
Kylie M Drake E Cristy Ruteshouser Rachael Natrajan Phyllis Harbor Jenny Wegert Manfred Gessler Kathy Pritchard-Jones Paul Grundy Jeffrey Dome Vicki Huff Chris Jones Micheala A Aldred

PURPOSE Wilms' tumor is a childhood cancer of the kidney with an incidence of approximately 1 in 10,000. Cooccurrence of Wilms' tumor with 2q37 deletion syndrome, an uncommon constitutional chromosome abnormality, has been reported previously in three children. Given these are independently rare clinical entities, we hypothesized that 2q37 harbors a tumor suppressor gene important in Wilms' tum...

2008
Mohammad Ali Ehsani M. Faranoush G. R. Bahoush A. Mehrvar S. Hejazi P. Vossough

Wilms tumor is the most common childhood renal tumor accounting for about 6% of pediatric malignant disease. Most patients with Wilms tumor can be cured with treatment and subsequently lead normal life. The multidisciplinary management of Wilms tumor has resulted striking improvement in survival of more than 85% nowadays and has become a paradigm for successful cancer therapy. We describe the r...

Journal: :Journal of the National Cancer Institute 2000
N Rahman L Arbour R Houlston C Bonaïti-Pellié F Abidi J Tranchemontagne D Ford S Narod K Pritchard-Jones W D Foulkes C Schwartz M R Stratton

Wilms tumor is an embryonal kidney cancer that affects one in 10 000 children. Epidemiologic studies have shown that 1%–3% of cases of Wilms tumor are familial and that a predisposition to Wilms tumor is probably caused by rare germline mutations acting in a dominant fashion (1). The risks of Wilms tumor conferred by mutations in these genes are poorly characterized, with estimates of their pen...

Journal: :DMW - Deutsche Medizinische Wochenschrift 1880

امانپور, سعید, ریسمانچی, ساناز, عقابیان, محمدعلی, محمدنژاد, احد, محمدنژاد, صمد, واسعی, محمد, کجباف زاده, عبدالمحمد, تیرگری, فرخ , حدادی, مهناز , محسنی, محمدجواد ,

  Background : Wilms' tumor (nephroblastoma) is the most common renal malignancy of childhood. This cancer is considered as an embryonal neoplasm that arises from nephrogenic blastemal. Despite advances in therapeutic success, survival rate is still not satisfactory in tumors with unfavorable histology and recurrent cases. On the other hand, late adverse effects of chemotherapy threaten the lif...

Journal: :Journal of the National Cancer Institute 2001
J D Ravenel K W Broman E J Perlman E L Niemitz T M Jayawardena D W Bell D A Haber H Uejima A P Feinberg

BACKGROUND Loss of imprinting (LOI) of the insulin-like growth factor-II (IGF2) gene, an epigenetic alteration associated with expression of the normally silent maternal allele, was observed first in Wilms tumor. Although LOI has subsequently been detected in most adult tumors, the biologic role of LOI in cancer remains obscure. We analyzed the imprinting status of Wilms tumors with respect to ...

2008
Sinescu Ioanel Hârza Mihai Şerbănescu Bogdan Gîngu Constantin Ştefan Bogdan Dudu Cătălin

INTRODUCTION Bilateral Wilmns' tumors with an unfavorable histology requires a combined treatment (extensive surgery, polychimiotherapy, radiotherapy). OBJECTIVE Presentation of the first renal transplant performed in Romania in a child with bilateral Wilms' tumor, at 3 years and 4 months after the end of a multimnodal treatment. MATERIAL AND METHODS Patient C. N., born on 30.04.1998, was d...

2014
Dinesh Rakheja Kenneth S. Chen Yangjian Liu Abhay A. Shukla Vanessa Schmid Tsung-Cheng Chang Shama Khokhar Jonathan E. Wickiser Nitin J. Karandikar James S. Malter Joshua T. Mendell James F. Amatruda

Wilms tumour is the most common childhood kidney cancer. Here we report the whole-exome sequencing of 44 Wilms tumours, identifying missense mutations in the microRNA (miRNA)-processing enzymes DROSHA and DICER1, and novel mutations in MYCN, SMARCA4 and ARID1A. Examination of tumour miRNA expression, in vitro processing assays and genomic editing in human cells demonstrates that DICER1 and DROS...

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