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Wilms Tumor

Urologic Clinics of North America, 2023
Wilms tumor (WT), or nephroblastoma, is the most common primary malignant renal tumor of childhood. It is an embryonal tumor that develops from remnants of immature kidney. There are approximately 500 new WT cases diagnosed in the United States every year.
Amanda F, Saltzman   +2 more
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WILMS' TUMOR

Pediatric Clinics of North America, 1997
Wilms' tumor is the most common renal malignancy of childhood. Survival rates for favorable histology of Wilms' tumor currently approach 90%. Recent advances in the molecular genetics of Wilms' tumor have led to insights into the genetic factors involved in the development of Wilms' tumor, normal renal development, and the mechanisms of tumorigenesis.
M J, Petruzzi, D M, Green
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Wilms' tumor

Pediatric Nephrology, 1992
In the last 2 decades, important advances in the treatment of Wilms' tumor have been made. The remarkable improvement in survival in these patients has been the product of new surgical techniques, classification of the tumors into prognostic stages upon initial presentation and the tailoring of chemotherapy and radiation therapy thus permitted. A brief
R P, Warrier, O, Regueira
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Wilms Tumor

Advances in Anatomic Pathology, 2014
Wilms tumor (WT) is the most common neoplasm of the kidney in children. It is an embryologic tumor that histologically mimics renal embryogenesis and is composed of a variable mixture of stromal, blastemal, and epithelial elements. Nephrogenic rests, generally considered to be precursor lesions of the WT, are foci of the embryonic metanephric tissue ...
Turki, Al-Hussain   +2 more
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Wilms’ Tumor

Hematology/Oncology Clinics of North America, 1987
The clinical presentation and approach to the management of Wilms' tumor in children were reviewed. In addition, recent studies of chromosomal abnormalities in Wilms' tumor, histopathologic findings as they effect prognosis and design of treatment, controversial issues in therapy, and the long-term effects of treatment of this childhood tumor were ...
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Bilateral Wilms’ Tumor

Journal of Urology, 1986
Recent studies indicate a favorable outcome with bilateral Wilms' tumor. From 1971 to 1985, ten children between the ages of 6 months and 5 years were treated for this disease. During the early part of the series, five patients had nephrectomy on one side and partial nephrectomy on the other side, and one patient had bilateral partial nephrectomies at ...
O P, Tucker   +4 more
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Extrarenal wilms tumor

Journal of Surgical Oncology, 1983
AbstractA retroperitoneal extrarenal Wilms tumor arising from an embryonic crest of renal tissue on a 10‐year‐old boy is reported. The histogenesis of such tumor is discussed.
Y G, Adam   +4 more
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Wilms tumor genes

Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1993
Multiple 'WT' genes exist. The WT1 gene at chromosomal band 11p13 has been cloned and is known to be important in the etiology of at least some tumors by virtue of the identification of both germline and somatic mutations in WT patients. Genes at 11p15 and 16q are also involved, either as initiating or tumor progression events.
V, Huff, G F, Saunders
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Extrarenal Wilms' tumor

Journal of Pediatric Surgery, 1989
A rare case of retroperitoneal extrarenal Wilms' tumor with an unusual presentation is reported. The tumor contained a large cystic component and mimicked ascites clinically.
K L, Narasimharao   +6 more
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Extrarenal Wilms' Tumor

Archives of Pediatrics & Adolescent Medicine, 1979
Extrarenal Wilms' tumor is a rare entity usually seen as a mass in the retroperitoneal area. It may surround and distort otherwise normal kidneys and ureters. Like many other abdominal masses, its true nature remains uncertain until microscopic examination has been performed after surgery.
R G, McCauley   +3 more
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