41. Wilms Tumor Alternative Names. nephroblastoma; Kidney tumor. Causes. Wilms tumor is one ofthe most common tumors of the abdomen in children and the most common type http://www.ehendrick.org/healthy/001575.htm

Injury Disease Nutrition Poison ... Prevention Wilms' tumor Definition Wilms' tumor is a cancerous tumor of the kidney that occurs in children. Alternative Names Nephroblastoma; Kidney tumor Causes Wilms' tumor is one of the most common tumors of the abdomen in children and the most common type of kidney tumor. The exact cause of tumor formation in most children is unknown. It is associated with certain birth defects including urinary tract abnormalities, absence of the iris (aniridia), and hemihypertrophy (enlargement of one side of the body). It is more common among some siblings and twins, which suggests a possible genetic cause. The tumor may become quite large, but usually remains encapsulated (self-enclosed). It may spread to other body tissues, especially the lungs. The disease is estimated to occur in about 1 out of 200,000 to 250,000 children. The peak time of occurrence is at 3 years old, and Wilms' tumor is rare after the age of 8 years. Review Date: 4/23/2004 Reviewed By: Samuel Blackman, M.D., Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH. Review provided by VeriMed Healthcare Network. A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

42. Ren Tum Completely necrotic ( chemotherapy ) nephroblastoma standard, Triphasicnephroblastoma. Necrotic 10% left ( post chemotherapy ) nephroblastoma http://www.anapath.necker.fr/site/SLMos/SLMos.data/Composants/Topics/Malign/RenT

Renal tumors of childhood Low risk tumors favorable Cystic nephroblastoma Fibroadenomatous-like pattern nephroblastoma Highly differentiated epithelial nephroblastoma Completely necrotic ( chemotherapy ) nephroblastoma Mesoblastic nephroma Intermediate risk tumors standard Triphasic nephroblastoma Necrotic 10% left ( post chemotherapy ) nephroblastoma Homologous: Blastema, tubules, glomeruli Heterologous: striated muscle... High risk tumors unfavorable Anaplasia in nephroblastoma Clear cell sarcoma Others Cystic nephroma Renal cell carcinoma Others

43. Nephroblastoma - General Practice Notebook nephroblastoma. Wilms tumour is a mixed neoplasm composed of metanephric blastemawith stromal and epithelial derivatives at various stages of http://www.gpnotebook.co.uk/cache/563740683.htm

nephroblastoma Wilms' tumour is a mixed neoplasm composed of metanephric blastema with stromal and epithelial derivatives at various stages of differentiation. Click here for more information...

44. Penn State Faculty Research Expertise Database (FRED) , A malignant kidney tumor made up of three cell typesblastemal, stromal, and epithelial, but not all present in every case.......nephroblastoma. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D009396

45. Clinical Cancer Research -- Sign In Page Expression and prognostic value Of CD44 isoforms in nephroblastoma (Wilms tumor).J Urol 2002;1686816.Medline; Ghanem MA, Van der Kwast TH, http://clincancerres.aacrjournals.org/cgi/content/full/10/22/7785

HOME HELP FEEDBACK SUBSCRIPTIONS ... Molecular Cancer Research This item requires a subscription to Clinical Cancer Research Online. Full Text MIB-1 and p27 Expression in Nephroblastoma Jones et al. Clin Cancer Res. This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Jones, C. Articles by van Steenbrugge, G. J. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 1 day for US$15.00 SitePass - You may access all content in Clinical Cancer Research Online (from the computer you are currently using) for 24 hours for US$25.00. Regain Access - You can regain access to a recent Pay per Article or SitePass purchase if your access period has not yet expired.

46. Clinical Cancer Research -- Sign In Page http://clincancerres.aacrjournals.org/cgi/reprint/10/22/7785

HOME HELP FEEDBACK SUBSCRIPTIONS ... Molecular Cancer Research This item requires a subscription to Clinical Cancer Research Online. PDF MIB-1 and p27 Expression in Nephroblastoma Jones et al. Clin Cancer Res. This Article Full Text (HTML) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Jones, C. Articles by van Steenbrugge, G. J. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 1 day for US$15.00 SitePass - You may access all content in Clinical Cancer Research Online (from the computer you are currently using) for 24 hours for US$25.00. Regain Access - You can regain access to a recent Pay per Article or SitePass purchase if your access period has not yet expired.

47. Nephroblastoma Topic - Unified Search Environment pediatric nephroblastoma originating from embryonic kidney stem cells; usuallyaffects children before the fifth year, but may occur in the fetus or rarely http://www.use.hcn.com.au/portals/shared/subject.`Nephroblastoma`/home.html

Nephroblastoma Topic Tree Definition: pediatric nephroblastoma originating from embryonic kidney stem cells; usually affects children before the fifth year, but may occur in the fetus or rarely in later life; caused by defects in one or more tumor suppressor genes. Synonyms and Source Vocabularies: Nephroblastoma Wilm's tumor KIDNEY, ADENOMYOSARCOMA, EMBRYONAL RENAL CANCER, WILMS KIDNEY, CARCINOSARCOMA, EMBRYONAL KIDNEY, EMBRYOMA KIDNEY, EMBRYONAL MIXED TUMOR Wilms Tumor Wilms' tumor and other childhood kidney tumors Nephroma Kidney Neoplasms Carcinoma, Renal Cell Nephroblastoma WAGR Syndrome Denys-Drash Syndrome Nephroma, Mesoblastic Neoplastic Syndromes, Hereditary ... Multiple Endocrine Neoplasia Nephroblastoma WAGR Syndrome Denys-Drash Syndrome Peutz-Jeghers Syndrome Adenomatous Polyposis Coli ... Myoepithelioma Nephroblastoma WAGR Syndrome Denys-Drash Syndrome Thymoma Adenomyoma ... Rhabdoid Tumor

48. Wilm's Tumor Or Nephroblastoma This type of cancer starts in the kidney. It is the most common type of kidneycancer in children but is very different from kidney cancer in adults. http://pediatrics.about.com/od/childhoodcancer/g/wilms_tumor.htm

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49. Nephroblastoma --  Encyclopædia Britannica nephroblastoma malignant renal (kidney) tumour of early childhood. In 75 percentof the cases, the tumour grows before the age of five; about twothirds of http://www.britannica.com/eb/article?tocId=9055297

50. Nephroblastoma (Wilms' Tumour) (from Renal System Disease) --  Encyclopædia Br nephroblastoma (Wilms tumour) (from renal system disease) nephroblastoma is aless common, but nevertheless an important, tumour in childhood, http://www.britannica.com/eb/article-58662?query=Kench cure&ct=

51. Tumors WilmsID5034 Citation. This paper should be referenced as such . Miozzo M . Kidneynephroblastoma (Wilms tumor). Atlas Genet Cytogenet Oncol Haematol. November 1998 . http://www.infobiogen.fr/services/chromcancer/Tumors/WilmsID5034.html

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumours ... NA Kidney: Nephroblastoma (Wilms tumor) Clinics and Pathology Etiology Wilms tumours are either sporadic or familial (1-2%); it may be associated with hemihypertrophia or genitourinary malformations (10%) and part of a recognized syndrome (2%). the syndromes predisposing to Wilms tumours are: WAGR (Wilms tumour, aniridia, genitourinary abnormalities and mental retardation), DDS (Denys-Drash syndrome: mesangial sclerosis, male pseudohermaphrodism and Wilms tumours), BWS (Beckwith-Weideman: exomphalos, macroglossia, gigantism) and SGBS (Simpson Golabi Behemel syndrome: overgrowth, mental impairment, craniofacial anomalies). Epidemiology the most common paediatric cancer of the kidney, affecting 10/10 children; 50% of cases occurs before the age of 3 yrs and 90% before 6 yrs. Clinics the localization is primarily the kidney, the incidence of bilateral involvement is 5- 10% blastematous tissue with some differentiated glomerular structures associated with mesenchymal tissue and tubules. Courtesy Pierre Bedossa Pathology Wilms tumours show a mimicry of nephrogenesis as the tumour comprises undifferentiated blastemal cells, differentiated epithelial cells and stromal cells; ectopic components, particularly skeletal muscle, are observed in 5-10% of tumours; the presence of identical deletions of WT1 in all components of some sporadic Wilms tumours suggests that the stromal components are neoplastic, raising the possibility that undifferentiated blastema cells are precursors of the stromal and heterologous elements.

52. NOV - Nephroblastoma Overexpressed Gene - Aka: IGFBP9 - Cancer GeneticsWeb NOV; nephroblastoma overexpressed gene. Location 8q24.1 Alias IGFBP9. Return toNOV Contents. Gene Database Entries for NOV http://www.cancerindex.org/geneweb/NOV.htm

Cancer Genetics Web www.cancer genetics.org NOV ; Nephroblastoma overexpressed gene (8q24.1) NOV Menu Summary Information - NOV Gene Database Entries for NOV Other NOV Related Resources Feedback / suggest a new topic for NOV Search: Summary Information NOV; Nephroblastoma overexpressed gene Location: Alias: Return to NOV Contents Gene Database Entries for NOV OMIM GeneCard (Weizmann Institute) Genbank Swiss-Prot Locus Link UniGene ... Nomenclature (search for NOV) Return to NOV Contents Other Related Resources Search Medline for related articles (PubMed) Medline Search: cancer AND gene AND (NOV[TI] OR IGFBP9[TI]) (PubMed) Limit search to: [Last Year] Limit search to: [Last 2 Years] Limit search to: [Reviews] Related Internet Resources (Guide to Internet Resources for Cancer) Kidney Ca. / Wilm's Tumour Genetics Kidney Ca. / Wilm's Tumour : Clinical and Epidemiological Information Return to NOV Contents [Home]

53. Current Controlled Trials - Search The ISRCTN Register Of Clinical Trials. Title of trial/grant title, nephroblastoma Clinical Trial and Study All localiseddisease nephroblastoma patients age more than 6 months or less than 18 http://www.controlled-trials.com/isrctn/trial/|/0/16583459.html

Welcome CCT User 9 September 2005 Trial registration Unique identification scheme International databases OAS_RICH('Top'); home my details ISRCTN Register m ... press Find an ISRCTN ISRCTN Find trials ISRCTN Register browse trials by title tips on searching Registration apply for ISRCTN Information introduction why register trials? ISRCTN FAQs data set ... Print-friendly version Nephroblastoma Clinical Trial and Study ISRCTN Title of trial/grant title Nephroblastoma Clinical Trial and Study Acronym SIOP 2001 Serial number at source N/A Study hypothesis N/A Disease or condition Nephroblastoma Participants - inclusion criteria 1. All localised disease nephroblastoma patients age more than 6 months or less than 18 years at time of diagnosis 2. Unilateral tumour with clinical and ultrasonic characteristics compatible with nephroblastoma or biopsy proven histological diagnosis 3. Written informed consent and national ethical committee approval 4. Stage II and III intermediate risk histology after pre-treatment according to protocol and after operation Participants - exclusion criteria All other kind of renal tumours of infancy. Patients without previous anti-tumour treatment.

54. Chicken Nephroblastoma Pages Chicken nephroblastoma Pages. PAGES IN CONSTRUCTION, improvements will be deathlikefast! Introduction nephroblastoma library details; Histology http://www.img.cas.cz/nfbl/

Chicken nephroblastoma Pages PAGES IN CONSTRUCTION, improvements will be deathlike fast! Introduction Nephroblastoma library details Histology Search MAV integration sites BLAST search MAV integration sites Publications Discussion Deviant´s World Talk to me :-) Last modified: Thu Jul 1 16:20:28 EDT 2004

55. Nephroblastoma Library Details PAGE IN CONSTRUCTION. Back to main page. http://www.img.cas.cz/nfbl/library.html

PAGE IN CONSTRUCTION Back to main page

56. Canine Spinal Nephroblastoma -- Macri Et Al. 33 (4): 302 -- Journal Of The Ameri Extradural Spinal, Bone Marrow, and Renal nephroblastoma J. Am. Anim. Hosp. Possible Intraspinal Metastasis of a Canine Spinal Cord nephroblastoma http://www.jaaha.org/cgi/content/abstract/33/4/302

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Macri, N. Articles by Coolman, R. Journal of the American Animal Hospital Association, Vol 33, Issue 4, 302-306 Articles Canine spinal nephroblastoma NP Macri, W Van Alstine, and RA Coolman An eight-month-old, female, mixed-breed dog was presented with bilateral hind-limb paralysis that reportedly developed over a two-to-three week period and was not associated with trauma. Plain radiographs of the spinal column were unremarkable, and a myelogram outlined an intramedullary mass of the spinal cord at the first lumbar (L1) vertebra. A hemilaminectomy was performed, and a mass that was identified histologically as nephroblastoma was excised from the spinal cord. Following surgery, the dog became fully ambulatory, and at 22 months postsurgery she remains clinically normal. The diagnosis, treatment, progression, histogenesis, and pathology of canine nephroblastoma are discussed. This article has been cited by other articles: A. M. Gasser, W. W. Bush, S. Smith, and R. Walton

57. Treatment Of Renal Nephroblastoma In An Adult Dog -- Seaman And Patton 39 (1): 7 Reported treatments of renal nephroblastoma in the dog have not described diseasefree Extradural Spinal, Bone Marrow, and Renal nephroblastoma http://www.jaaha.org/cgi/content/abstract/39/1/76

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Full Text Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Seaman, R. L. Articles by Patton, C. S. Journal of the American Animal Hospital Association American Animal Hospital Association Case Report Treatment of Renal Nephroblastoma in an Adult Dog Rebecca L. Seaman, DVM and Clark S. Patton, DVM, MS From the Departments of Small Animal Clinical Sciences (Seaman) and Pathology (Patton), College of Veterinary Medicine, University of Tennessee, Box 1071, Knoxville, Tennessee 37901-1071. An 8-year-old Labrador retriever was diagnosed with a unilateral malignant nephroblastoma and hypertrophic osteopathy. The histopathologically malignant tumor was confined to the renal capsule, but the sarcomatous

58. Cancer Syndromes Additional features Wilms tumor (nephroblastoma), gonadoblastoma, Wilms Tumor (nephroblastoma) most common childhood abdominal malignancies. http://ibis-birthdefects.org/start/cancersy.htm

Tips for printing Cancer Syndromes About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and Nephroblastoma Aniridia,Type II Wims Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Wilms Tumor 3 Wilms Tumor 2 Multiple Tumor Associated Chromosome Region 1 Special Resources Cancer Syndrome A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Groups [Ukrainian] Online Mendelian Inheritance in Man by OMIM ANIRIDIA ... ANIRIDIA, CEREBELLAR ATAXIA ... WAGR SYNDROME ... ANIRIDIA AND ABSENT PATELLA ... WILMS TUMOR 1 ... ECTOPIA PUPILLAE ... CAT EYE SYNDROME ... PETERS ANOMALY ... EXOSTOSES ... SPLIT-HAND/FOOT ... Wilms Tumor Nephroblastoma by OMIM Rather numerous instances of multiple sibs with Wilms tumor have been described ... The syndrome of aniridia, hemihypertrophy and other congenital anomalies with Wilms tumor, subsequently known as the WAGR syndrome, was first described by Miller et al. (1964) ... . Riccardi et al. (1978) observed a triad of aniridia, ambiguous genitalia and mental retardation (AGR triad) in 3 patients with an interstitial deletion of the short arm of chromosome 11 ... Marshall et al. (1982) studied 14 patients with aniridia .... 6 had interstitial deletion of 11p of various lengths. Band 11p13 was included in the deletion in all 6 cases ...

59. TUMOR CLASSIFICATION FRONTIERS IN BIOSCIENCE;. DATA FORM FOR CANCER CLASSIFICATION nephroblastoma (WILMS TUMOR). HISTOPATHOLOGIC TYPE. nephroblastoma http://www.bioscience.org/atlases/tumpath/class/nephrobl.htm

FRONTIERS IN BIOSCIENCE; DATA FORM FOR CANCER CLASSIFICATION - NEPHROBLASTOMA (WILMS' TUMOR) HISTOPATHOLOGIC TYPE Nephroblastoma Comments:

60. TUMOR STAGING FRONTIERS IN BIOSCIENCE;. DATA FORM FOR CANCER STAGING nephroblastoma. Form 785-1-056. CLIN, PATH, DEFINITIONS. PRIMARY TUMOR (T) http://www.bioscience.org/atlases/tumpath/staging/nephrobl.htm

FRONTIERS IN BIOSCIENCE; DATA FORM FOR CANCER STAGING - NEPHROBLASTOMA Form # 785-1-056 CLIN PATH DEFINITIONS PRIMARY TUMOR (T) TX Primary tumor cannot be assessed No evidence of primary tumor Unilateral tumor 80 cm or less in area (including kidnes)* Unilateral tumor more than 80 cm in area (including kidney)* Unilateral tumor rupture before treatment Bilateral tumors *Note: The area is calculated by multiplying the vertical and horizontal dimensions of the radiologic shadow of the tumor and kidney. LYMPH NODE (N) NX Regional lymph nodes cannot be assessed No regional lymph node metastasis Regional lymph node metastasis DISTANT METASTASIS (M) MX Presence of distant metastasis cannot be assessed No distant metastasis Distant metastasis PRIMARY TUMOR (PT) pTX Primary tumor cannot be assessed No evidence of primary tumor Intrarenal tumor completely encapsulated; excision complete and margins histologically free Tumor invades beyond the capsule or renal parenchyma;* excision complete

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