Brusa-Torricelli Syndrome (www.whonamedit.com) A congenital syndrome in which aniridia (congenital absence of the iris) and nephroblastoma (Wilms' tumour) is http://www.whonamedit.com/synd.cfm/2404.html
Extractions: A congenital syndrome in which aniridia (congenital absence of the iris) and nephroblastoma (Wilms' tumour) is associated with mental retardation, craniofacial defects (microcephaly), growth retardation and skeletal anomalies, deformed pinna, genitourinary anomalies, hamartomas, and umbilical and inguinal hernias. Other frequent features include cataract and glycoma, hypospadias, hemihypertrophy, and horseshoe kidney. The syndrome affects both sexes but is more frequent in males.
Nephroblastoma, [s8]uncommon Primary Surgery Volume One Nontrauma After Burkitt's lymphoma, nephroblastoma is the commonest solid tumour of childhood in Africa (in Caucasians it is the fourth commonest). congenital anomalies (eye defects, hemihypertrophy, and urinogenital anomalies), which are sometimes associated with a nephroblastoma. http://www.meb.uni-bonn.de/dtc/primsurg/docbook/html/x11710.html
Extractions: Primary Surgery: Volume One: Non-trauma Prev Chapter 18. Primary oncology Next NEPHROBLASTOMA THE DIFFERENTIAL DIAGNOSIS includes hydronephrosis (often bilateral), polycystic disease of the kidneys (uncommon, haematuria is usual), or a neuroblastoma displacing the kidney downwards (rare in Africa). Prev Home Next Non-Hodgkin's lymphoma, [s8]uncommon Up Retinoblastoma, [s8]uncommon
1Up Health > Diseases & Conditions > N nephroblastoma, see Wilms tumor; Nephrocalcinosis; Nephrogenic diabetesinsipidus congenital, see congenital nephrogenic diabetes insipidus; http://www.1uphealth.com/health/disease_n.html
Extractions: Nabothian cyst Nails - fungal infection, see Fungal nail infection NALD, see Adrenoleukodystrophy Narcissistic personality disorder Narcolepsy Nasal allergies, see Allergic rhinitis Nasal polyps Nasal tumor, see Juvenile angiofibroma Natural short sleeper NBP, see Prostatitis - nonbacterial Nearsightedness NEC, see Necrotizing enterocolitis Necrosis - acute tubular, see Acute tubular necrosis Necrosis - renal papillae, see Renal papillary necrosis Necrosis - renal tubular, see Acute tubular necrosis Necrotizing colitis , see Pseudomembranous colitis Necrotizing enterocolitis Necrotizing fasciitis, see Necrotizing soft tissue infection Necrotizing glomerulonephritis, see Rapidly progressive (crescentic) glomerulonephritis Necrotizing granuloma Necrotizing pneumonia, see Aspiration pneumonia Necrotizing soft tissue infection Necrotizing vasculitis Neonatal adrenoleukodyrstophy, see Adrenoleukodystrophy Neonatal conjunctivitis Neonatal polycythemia , see
Mesoblastic Nephroma This is a rare, usually congenital, neoplasm of the kidney. cystic nephroma, cystic partially differentiated nephroblastoma, cystic nephroblastoma, and cystic clear cell sarcoma of http://www.thedoctorsdoctor.com/diseases2/kidney_mesoblastic_nephroma.htm
Samuel M. Mahaffey, M.D. of childhood; congenital diaphragmatic hernia; congenital and acquired anomalies stenosis; Gastroschisis; Omphalocele; Neuroblastoma; nephroblastoma (Wilm' tumor); Ovarian tumors http://surgery.duke.edu/people/mahaf001.html
Extractions: Pediatric trauma and critical care; solid tumors of childhood; Congenital diaphragmatic hernia; congenital and acquired anomalies of the lung, chest, neck, or abdomen; Intestinal atresia; Intestinal duplications; Hypertrophic pyloric stenosis; Gastroschisis; Omphalocele; Neuroblastoma; Nephroblastoma (Wilm' tumor); Ovarian tumors in children; Research Interests
Cancer Syndromes nephroblastoma. by OMIM. Rather numerous instances of multiple sibs with Wilms tumor have been described The syndrome of aniridia, hemihypertrophy and other congenital http://www.ibis-birthdefects.org/start/cancersy.htm
Extractions: 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 ...
Extractions: Gross Morbid Pathology of Swine C. L. Davis Foundations Gross Morbid Anatomy of Diseases of Animals April 9-13, 2001, AFIP, Washington, DC. Dr. vet. Med. Matti Kiupel, MS, DACVP Animal Disease Diagnostic Laboratory and Department of Veterinary Pathobiology Purdue University, West Lafayette, IN tomcat@purdue.edu No. Tissue Etiology/Disease Gross Diagnosis Notes CAROUSEL 1 INTRODUCTION CL Davis Logo Picture ADDL/Logo Word slide Traditional Technologies: Evolution in Management Technologies: Small farms; 50-100 sows Large farms; 1000-5000 sows Group farrowing; 2-4 gps/yr Reduced weaning age; 10-21 days-of-age Weaning age: 4-8 weeks-of-age Age-segregated rearing; AI/AO, SEW Continuous-flow rearing Site-segregated rearing; 2- or 3-site Word slide Ages/stages: Suckling 1-2 mo.; Grow/Fin. 3-6 mo.; Breeding/Adult Word slide Outline NEOPLASIA Kidney Lymphosarcoma Multifocal renal lymphoma All ages and sexes; multicentric or thymic Kidney, renal ln. Lymphosarcoma Multifocal to coelescing renal lymphoma Head, sagittal
CYSTIC PARTIALLY DIFFERENTIATED NEPHROBLASTOMA (CPDN) INTRODUCTION Cystic Partially Differentiated nephroblastoma (CPDN), is a rare, circumscribed theyare congenital or acquired nonneoplastic abnormalities and; http://www.bhj.org/journal/1996/3804_oct/case_893.htm
Congenital Malformations Causes of Malformations. Most congenital abnormalities do not have s ingle problembut are caused by Very low cure rate ( 5%). Wilms Tumor (nephroblastoma). http://rossmed.hypermart.net/notes/semesterthree/pedpath.htm
Extractions: Matchmaker.com: Sign up now for a free trial. Date Smarter! Get advertisers for your website. Congenital Malformations (From Dr. Tomlinsons path lecture, 9 Nov 2000, by Brian Buschman Return to Semester Three Goodies Return to The Unofficial Ross Page Malformations are morphological problems that come along from the beginning. These include things like congenital heart disease. Deformations are defects arising later as problems from mechanical factors. These may be things like forces from leiomyomas or hydro- related factors. Disruptions are a destruction of a body part that began proper formation but something went wrong. This may include amniotic bands. Sequence refers to multiple congenital problems all secondary to a common cause. The most notable being oligohydraminos (Potters) sequence. Oligohydraminos causes fetal compression and problems with fancies, hands/feet and pulmonary hypoplasia. Most congenital abnormalities do not have s ingle problem but are caused by: Genetic causes Multifactoral causes The timing of the insult is most serious with the critical period being around the 4th or 5th week of pregnancy.
Mesoblastic Nephroma The group of tumors with a better prognosis encompasses congenital mesoblasticnephroma (CMN), fetal rhabdomyomatous nephroblastoma and cystic, partially http://www.thedoctorsdoctor.com/diseases/kidney_mesoblastic_nephroma.htm
Extractions: Hypercalcemia in association with mesoblastic nephroma: report of a case and review of the literature. Ferraro EM, Klein SA, Fakhry J, Weingarten MJ, Rose JS. Pediatr Radiol 1986;16(6):516-7 Abstract quote Hypercalcemia, often associated with certain types of adult tumors, has also been described in pediatric neoplasms. In childhood, the more common associations include lymphoma, leukemia, rhabdomyosarcoma and rarely neuroblastoma. However, recently, several infants with hypercalcemia were described having renal tumors without bone metastases. The following is a case report of a 2-month-old infant who presented with severe hypercalcemia and a large right-sided abdominal mass, which at surgery was diagnosed as a cellular mesoblastic nephroma.
Www.whonamedit.com syndrome). A congenital syndrome in which aniridia and nephroblastoma(Wilms' tumour) is associated with multiple abnormalities. Aniridia http://www.whonamedit.com/syndlist.cfm/193
Extractions: Aase-Smith syndrome A familial deformity syndrome. Aases syndrome (Aase-Smith syndrome) A familial deformity syndrome. Alè-Calò syndrome (Langer-Giedion syndrome) Syndrome characterized by a combination of mental retardation and a long list of physical abnormalities, including multiple extoses, peculiar facies, and loose redundant skin. Alfi's syndrome A very rare chromosome anomaly also known as monosomy 9P. Aniridia-Wilms' tumor association (Brusa-Torricelli syndrome) A congenital syndrome in which aniridia and nephroblastoma (Wilms' tumour) is associated with multiple abnormalities. Aniridia-Wilms tumour syndrome (Brusa-Torricelli syndrome) A congenital syndrome in which aniridia and nephroblastoma (Wilms' tumour) is associated with multiple abnormalities. Appelt-Gerken-Lenz syndrome (Roberts' pseudothalidomide syndrome) A syndrome of multiple congenital abnormalities. Audrys syndrome I (Hallermann-Streiff-François syndrome) A syndrome of multiple congenital abnormalities comprising an abnormally shaped skull, proportionate dwarfism, birdlike facies, atrophy of the skin, bilateral microphtalmia, mental retardation and congenital cataracts.
Cancer Syndromes WAGR) syndrome; Wilms tumor associated with congenital absence of Additional featuresWilms tumor (nephroblastoma), gonadoblastoma, hemangioma, and pigmented http://ibis-birthdefects.org/start/cancersy.htm
Extractions: 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 ...
Uhrad.com - Pediatric Imaging Teaching Files Peds Case Forty Seven Small Bowel Rupture. Peds Case Forty Eight - Wilm's Tumor(nephroblastoma). Peds Case Sixty - congenital Adenomatoid Malformation. http://www.uhrad.com/pedsarc.htm
Uhrad.com - Pediatric Imaging Teaching Files Discussion Wilm's tumor (nephroblastoma) is the most common Associated conditionsinclude congenital genitourinary malformations, hemihypertrophy, sporadic http://www.uhrad.com/pedsarc/peds048.htm
Extractions: Click on Images for Enlarged View Clinical History: 18-month-old female with palpable abdominal mass. Findings: Ultrasound: Large inhomogeneous mass arising from the upper right kidney. Multiple areas of decreased echogenicity are present compatible with necrosis. MRI: The mass demonstrates heterogeneous low T1 and high T2 signal characteristics with areas of high T1 signal corresponding with hemorrhage. A pseudocapsule is evident on T2 imaging. There is no involvement of the renal vein or IVC. Diagnosis: Wilm's tumor (nephroblastoma). Discussion: Wilm's tumor (nephroblastoma) is the most common abdominal malignancy, and the most common solid renal mass in childhood. The incidence is 1 in 10,000 with a bimodal peak at ages 2.5 and 3.5 years (1). There are both hereditary and sporadic forms, and approximately 6% are bilateral(1). Most are unicentric and arise from the kidney. Extra-renal Wilm's tumor is rare. Associated conditions include congenital genitourinary malformations, hemihypertrophy, sporadic aniridia, as well as Beckwith-Weidemann and Drash syndromes. nephroblastomatosis (residual metanephrogenic blastema beyond 36 weeks gestation) is also associated with Wilm's tumor and is considered by many its precursor.
Publikationen problems and complicationsevaluation of the nephroblastoma Study SIOP 9 D. SchmidtSuccessful therapy of local recurrence of congenital mesoblastic nephroma http://www.med-rz.uni-sb.de/med_fak/kinderklinik/Publikationen/body_publikatione
Congenital Mesoblastic Nephroma From Pediatrics / Oncology to a nonrenal lowgrade congenital infantile fibrosarcoma Fetal rhabdomyomatous nephroblastoma(monophasic Wilms tumor) nephroblastomatosis (nephrogenic rests http://author.emedicine.com/PED/topic3007.htm
Extractions: AUTHOR INFORMATION Section 1 of 12 Authored by Helen SL Chan, MBBS, FRCP(C), FAAP , Senior Scientist, Research Institute; Professor, Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Canada Helen SL Chan, MBBS, FRCP(C), FAAP, is a member of the following medical societies: American Academy of Pediatrics American Association for Cancer Research American Society of Clinical Oncology American Society of Hematology , and Royal College of Physicians and Surgeons of Canada Edited by Stephan A Grupp, MD, PhD , Director, Stem Cell Biology Program, Children's Hospital of Philadelphia; Assistant Professor, Department of Pediatrics, Division of Oncology, University of Pennsylvania; Mary L Windle, PharmD
Nephroblastoma: Some Details nephroblastoma Also known as Wilms tumour; Usually presents as a palpable abdominalmass in a otherwise well child; Associated with other congenital anomalies http://www.mds.qmw.ac.uk/biomed/kb/humandevelopment/stage2/learning landscapes/w
