Extractions: Waardenburg-Klein syndrome (ptosis-epicanthus) 270.2 Wagner's disease (colloid milium) 709.3 Wagner (-Unverricht) syndrome (dermatomyositis) 710.3 Waiting list, person on V63.2 Wakefulness disorder (see also Hypersomnia) 780.54 Waldenstrom's Waldenstrom-Kjellberg syndrome (sideropenic dysphagia) 280.8 Walking Wall, abdominal=see condition Wallenberg's syndrome (posterior inferior cerebellar artery) (see also Disease, cerebrovascular, acute) 436 Wallgren's Wandering acetabulum 736.39
Nephroblastoma - Part B TX. nephroblastoma (WILMS TUMOR). nephroblastoma Components and Patterns. neural.nephroblastoma Light microscopy and Ultrastructure. http://sup.ultrakohl.com/uscap/abs-1998/nephr-B.htm
Www.afip.org/vetpath/WSC/WSC94/94wsc28.txt congenital diverticula contain all layers of the intestinal wall, while Rhabdomyocyticnephroblastoma, bilateral, kidney, swine Histologic examination of 4 æm http://www.afip.org/vetpath/WSC/WSC94/94wsc28.txt
MUMS List Of Disorders - N - O nephroblastoma (kidney cancer) (1); Nephrocalcinosis (3); Nephrogenic Diabetes NeuropathyCongenital Hypomyelination (5) *; Neuropathy Hereditary Type II (2 http://www.netnet.net/mums/mum_n-o.htm
Nephroblastom Review Since that time the association of nephroblastoma and other different congenitalanomalies, notably aniridia hemihypertrophy and malformations of genitalia http://www.med-rz.uni-sb.de/med_fak/kinderklinik/Review/body_review.htm
Extractions: Prof. Dr. N. Graf Wilms´tumour or nephroblastoma was first described as a renal neoplasm by Rance in 1814 (1). In 1899 Max Wilms, a surgeon, wrote a detailed monograph "Die Mischgeschwülste der Niere" (2), that gave later this tumour his name. It is a tumour, that was always incurable in former days, but that is today one of the best curable malignancies. The improvement in treatment is based mainly on the progress of surgery, radiotherapy and in the development of effective chemo- therapeutics. Interdisciplinary teamwork and prospective randomised multicenter studies are clues for the achieved increase in prognosis. Epidemiology, Incidence Nephroblastoma, being 6 % of all malignancies in children, is the most common childhood renal tumour. The annual incidence rate of Wilms´tumour is 8 / 1.000.000 children under the age of 15 years, meaning that about 1 out of 100.000 children will suffer of this neoplasm. In Germany more than 100 new cases occur every year (3). The highest incidence rates are reported among United States blacks, in Finland and regions of France, the lowest rates are reported from Asia (4). World-wide the sex ratio is 1:1. The distribution of age at diagnosis peaks at 2 to 3 years in unilateral cases and is lower in children with a bilateral tumour. Bilateralisation will occur in 5 % of nephroblastoma (5). Aetiology and genetics In 1964 Miller et al. (6) reported for the first time of an association of Wilms´tumour and aniridia. Since that time the association of nephroblastoma and other different congenital anomalies, notably aniridia hemihypertrophy and malformations of genitalia (cryptorchidism, hypospadias, pseudohermaphroditism and gonadal dysgenesis) is well known. Aniridia and hemihypertrophy are extremely rare in the general population, and children with either of these conditions should be screened carefully for Wilms´tumour. The disease occurs in conjunction with neurofibromatosis, WAGR (Wilms´tumour, aniridia malformations of genitalia, retardation) Beckwith-Wiedemann (BWS), Drash (pseudohermaphroditism, glomerulopathy, and Wilms´tumour) and Perlman familial nephroblastomatosis (bilateral renal hamartomas, macrosomia, islet cell hypertrophy, unusual facial) malformation syndromes (7).
Archives Of The AFIP -- RadioGraphics 1995; 15: 653-669 BM, Mancer K. Magnetic resonance imaging of cystic, partially differentiated nephroblastoma. Congenitalmesoblastic nephroma of infancy report of a case with http://www.rsna.org/REG/publications/rg/afip/privateM/1995/0015/0003/0653/10.htm
Large Muscles Adrenal; nephroblastoma; Hepatoblastoma; Rhabdomyosarcoma; Wilms tumor; Congenitalgastric teratoma; Hemangiomas. GU Renal medullary dysplasia; Overgrowth of http://www.neuro.wustl.edu/neuromuscular/mother/mlarge.html
Wilms Tumor Alternate Names nephroblastoma; Kidney tumor. It is associated with certain congenitaldefects including urinary tract abnormalities, absence of the iris http://www.rwjhamilton.org/Atoz/encyclopedia/article/001575.asp
Extractions: Medical Encyclopedia Encyclopedia Disease W -> Wilms tumor Wilms tumor Alternate Names: Nephroblastoma; Kidney tumor Causes and Risks: Wilms tumor is one of the most common intraabdominal tumors in children and the most common type of kidney tumor. The exact cause of tumor formation is unknown, but it probably develops in fetal tissue. It is associated with certain congenital defects including urinary tract abnormalities, absence of the iris (aniridia) and hemihypertrophy (enlargement of one side of the body), and shows an increased incidence among 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. The frequency of disease occurrence is estimated to be about 1 out of 200,000 to 250,000 children. The peak incidence is at 3 years old. Rarely, the tumor may be present in adults. Symptoms: Abdominal pain Swelling in the abdomen (abdominal hernia or mass) Blood in the urine (occurs in less than 1/4 of children) Fever Loss of appetite Nausea Vomiting General discomfort or uneasiness ( malaise Blood pressure, high
Diagnostic Pathology Translate this page causes of nephrotic syndrome Post infectious, toxic, SLE, HUS, other congenitaldiseases (Nail patella syndrome, brain malformations, nephroblastoma). http://www.pathology.lsumc.edu/Pathist/RENAL/GLOMERULOPATHIES/24MSGD/MSGDb
DEPARTMENT OF PAEDIATRIC SURGERY Haemangioma; Lymphangioma the Hamartomatous tumours of childhood. Congenitalanomalies related to the branchial arches. nephroblastoma (Wilms tumour). http://web.uct.ac.za/depts/ich/teaching/undergrad/5th_year/surg5_01.htm
Extractions: Three major causes of death in childhood are surgical problems: Accidents Congenital malformations Malignancy Great process in the surgical care of neonates, infants and children has been made. Today Paediatric Surgery stands fully recognised as a speciality in its own right. Students are expected to study the following: Salient features of surgical disease In trying to grasp the important features of a large number of unfamiliar surgical conditions, it is easy to get side-tracked into a morass of minutiae. The student will make effective use of his limited time and energy by forcing him to concentrate upon the following aspects of each condition described above.
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Extractions: AU - Granzen B; Efferth T; Keller U; Beniers AJ; Mertens R; Jakse G; Fuzesi L TI - Differential expression of the drug resistance markers DNA topoisomerase II alpha and glutathione S-transferase-pi in the histological compartments of Wilms' tumors. SO - Anticancer Res 2001 Jan-Feb;21(1B):771-6 AD - Department of Children and Adolescents, University Hospital Aachen, Germany. AB - More than 80% of the patients presenting with Wilms' tumor can be cured today. Some patients, however, fail to respond to chemotherapy. The objective of this study was to analyze the immunohistochemical distribution of two markers of cytostatic drug resistance, e.g. DNA topoisomerase II alpha (Topo II alpha) and glutathione S-transferase-pi (GST-pi) in 23 Wilms' tumor patients who had undergone an operation between 1984 and 3 UI - 21125012 AU - McHugh K; Pritchard J TI - Problems in the imaging of three common paediatric solid tumours. SO - Eur J Radiol 2001 Feb;37(2):72-8 AD - Great Ormond Street Hospital for Children, London WC1N 3JH, UK. AB - Modern radiologic techniques have led to a more accurate diagnosis and staging in many paediatric malignancies. The optimal imaging of some tumours is not, however, well defined and needs to be constantly re-assessed. Similarly with evolving clinical treatment protocols, recommended imaging strategies should be continually re-evaluated. The significance of some findings on radiologic examinations in paediatric oncology patients is disputed. A number of issues relating to the imaging of Wilms', neuroblastoma and rhabdomyosarcoma in childhood are discussed.
Web Wombat World Directory Top Health Conditions and Diseases Cancer Genitourinary Kidney Wilm's_Tumor__Congenital_Nephroblastoma http://www.webwombat.com.au/wwdir/WW386759.HTM
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Directory Vaionline: Siti_Mondiali/Health/Conditions_and_Diseases/Cancer/Genitou directory.vaionline.it vi permette di accedere al directory di siti italiani. E' organizzato per aree geografiche e aree temeatiche. Fa parte del portale Vaionline che ti offre molti altri servizi. http://directory.vaionline.it/Siti_Mondiali/Health/Conditions_and_Diseases/Cance
Extractions: California Kidney Cancer Foundation - Founded to make new and advanced forms of therapy for kidney cancer readily available in Northern California. This site is about the facility, patient stories, treatments and resources. Kidney Cancer Association - Membership organization of patients, families, doctors, and health professionals in kidney cancer. Kidney Cancer Directory of OnTumor.com - A physician guided website for kidney cancer patients, their families, and caregivers. Your first stop for reliable cancer information on the web. Kidney Cancer Resource Web - Links and resources for patients and their families. Steve Dunn's Kidney Cancer Page - Information on kidney cancer, its diagnosis, prevention, and treatment, from the webpage of a former kidney cancer patient. Understanding the Facts and Myths of Kidney Cancer - General but detailed information for kidney cancer patients provided by physicians. What You Need to Know about Kidney Cancer - An important booklet from the National Cancer Institute for kidney cancer patients, their caregivers, and healthcare professionals.
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