Wilms' tumor
nephroblastom
nephroblastoma latin

Wilms' tumor, usually is reported in children under the age of 5.

It is still not clear what causes most Wilms' tumors.

Children who are at risk should be screened for Wilms' tumor every three months until they turn eight.

The majority of kidney cancers reported in children are Wilms' tumors.

Wilms' tumor is a rare type of kidney cancer that affects children.

Having certain genetic conditions or birth defects can increase the risk of developing Wilms' tumor.

He had Wilms' tumor, a cancer that originates in the kidney.

Kidney late effects may be caused by treatment for Wilms' tumor and other childhood cancers.

It has been associated with Wilms' tumor and brachydactyly.

Most children with Wilms' tumor can be cured.

For stage I Wilms' tumor, 1 or more of the following criteria must be met:

About 50% of patients develop Wilms' tumour.

People of African descent have the highest rates of Wilms' tumor.

An analysis of cases from the Third National Wilms' Tumor Study.

It can present somewhat differently in children, in whom it may be mistaken for Wilms' tumor.

Wilms' tumors may be separated into 2 prognostic groups based on pathologic characteristics:

Olivia, then aged six, suffered from Wilms' tumor.

Recently published management guidelines recommend regular abdominal ultrasounds up to age eight to detect Wilms' tumor.

Important It is possible that the main title of the report Wilms' Tumor is not the name you expected.

A mother's occupational exposure to pesticides during pregnancy is associated with an increases in her child's risk of leukemia, Wilms' tumor, and brain cancer.

Stage V Wilms' tumor is defined as bilateral renal involvement at the time of initial diagnosis.

At 16 months old, Shamsavari developed Wilms' tumor, a tumor of the kidneys.

In general, Wilms' tumor is curable.

Wilms' tumor is most common in children under the age of 5, but can rarely be diagnosed in older children or in adults.

Wilms' tumor or nephroblastoma is cancer of the kidneys that typically occurs in children, rarely in adults.

In 1898 he described the unitary nature of nephroblastoma.

Her main work has centred on pediatric oncology, especially nephroblastoma.

Wilms tumor, also known as Nephroblastoma, is a form of kidney cancer that occurs most often in children.

Grossly, MNs appear as solitary, unilateral masses indistinguishable from nephroblastoma.

Examples are nephroblastoma, medulloblastoma and retinoblastoma.

Wilms' tumor or nephroblastoma is cancer of the kidneys that typically occurs in children, rarely in adults.

Cystic partially differentiated nephroblastoma is a very rare type of Wilms tumor made up of cysts.

Pathologically, a triphasic nephroblastoma comprises three elements:

As a result of his extensive work involving renal tumors, another name for "nephroblastoma" is Wilms' tumor, a malignant tumor of the kidney.

Cystic partially differentiated nephroblastoma is a rare cystic variant of Wilms tumor (1%) with unique pathologic and clinical characteristics.

Bourdeaut F, Guiochon-Mantel A, Fabre M, et al.: Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders.

Sporadic aniridia mutations may affect the WT1 region adjacent to the AN2 aniridia region, causing a kidney cancer called nephroblastoma (Wilms tumor).

NOV (nephroblastoma overexpressed) also known as CCN3 is a matricellular protein that in humans is encoded by the NOV gene.

Blakely ML, Shamberger RC, Norkool P, et al.: Outcome of children with cystic partially differentiated nephroblastoma treated with or without chemotherapy.

Metanephric adenoma (MA)is a rare, benign tumour of the kidney, that can have a microscopic appearance similar to a nephroblastoma (Wilms tumours), or a papillary renal cell carcinoma.

Baker JM, Viero S, Kim PC, et al.: Stage III cystic partially differentiated nephroblastoma recurring after nephrectomy and chemotherapy.

Oberholzer HF, Falkson G, De Jager LC: Successful management of inferior vena cava and right atrial nephroblastoma tumor thrombus with preoperative chemotherapy.

Clear cell sarcoma of the kidney, rhabdoid tumor of the kidney, neuroepithelial tumor of the kidney, and cystic partially-differentiated nephroblastoma are childhood renal tumors unrelated to Wilms tumor.

Aniridia in some individuals is associated with kidney nephroblastoma (Wilms tumor), genitourinary anomalies, or mental retardation and cerebellar ataxia (Gillespie syndrome), resulting in the WAGR syndrome.

Szavay P, Luithle T, Semler O, et al.: Surgery of cavoatrial tumor thrombus in nephroblastoma: a report of the SIOP/GPOH study.

Weirich A, Ludwig R, Graf N, et al.: Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity.

Reinhard H, Schmidt A, Furtwängler R, et al.: Outcome of relapses of nephroblastoma in patients registered in the SIOP/GPOH trials and studies.

Jereb B, Burgers JM, Tournade MF, et al.: Radiotherapy in the SIOP (International Society of Pediatric Oncology) nephroblastoma studies: a review.