nephroblastoma oor Spaans

nephroblastoma

naamwoord
en
(oncology) A tumour affecting a kidney.

Vertalings in die woordeboek Engels - Spaans

nefroblastoma

Termium

Tumor de Wilms

en
rare disease
wikidata

tumor de Wilms

Termium

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voorbeelde

Advanced filtering
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Nephroblastoma (Wilms Tumor) Nephroblastomas (Wilms tumor) comprise more than 80% of renal tumors of childhood.
Y creo en tu pollaLiterature Literature
In the ACGT project the team focused on paediatric nephroblastoma, a childhood cancer of the kidney, and in particular on a trial run by SIOP, the International Society of Paediatric Oncology.
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There are several tumour types that occur almost exclusively in children including neuroblastoma, nephroblastoma, medulloblastoma and retinoblastoma.
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In a prospective study of 164 long-term survivors (median follow-up, 26 years), nephroblastoma (OR, 5.2) and neuroblastoma (OR, 6.5) survivors had more components of metabolic syndrome than did controls.
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The patient has a 13.8 Mb deletion lying through 8q23.1 to 8q24.13, nephroblastoma overexpressed (NOV) gene, is located 8q24.1.
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Wilms tumor (nephroblastoma)
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The name multicystic nephroma was first proposed in 1951 and later modified and further subdivided into cystic nephroma and cystic partially differentiated nephroblastoma depending on the absence and presence of blastemal element, respectively.
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Wilms tumor (also called Wilms’ tumor or nephroblastoma) is a type of cancer that starts in the kidneys.
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The most common types of childhood kidney cancer are Wilms tumour and nephroblastoma.
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Wilms' tumor (nephroblastoma) is a cancerous tumor of the kidney.
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Also known as nephroblastoma, it's the most common cancer of the kidneys in children.
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Patients with any type of nephrogenic rest in a kidney removed for nephroblastoma are considered at increased risk for tumor formation in the remaining kidney.
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The tumors that most frequently occur in the abdomen are nephroblastoma or Wilms tumor, Burkitt's lymphoma, neuroblastoma, and ovarian germ cell tumors.
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Cystic partially differentiated nephroblastoma is a very rare type are benign tumors made up of cysts.
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The WT1 protein contains a DNA binding domain and any deletions or point mutations of the WT1 gene which destroy this activity result in the development of the childhood nephroblastoma Wilms' tumor and Denys-Drash syndrome.
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Wilms tumor, also called nephroblastoma, is a malignant (cancerous) tumor originating in the cells of the kidney.
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Cystic partially differentiated nephroblastoma is a very rare type of Wilms tumor made up of cysts.
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Cystic Partially Differentiated Nephroblastoma is not cancer but may become Wilms tumor.
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Nephroblastoma; Kidney tumor - Wilms Causes
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Standard treatment options for cystic partially differentiated nephroblastoma include the following:
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In the present study, kidney cancer is distributed in all ages, rates reached age-specific incidence highest in the range of in both sexes should also be mentioned that in this group includes the nephroblastoma or Wilms tumor occurs in children.
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Grossly, mesoblastic nephromas appear as solitary, unilateral masses indistinguishable from nephroblastoma.
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Other types of childhood kidney tumors include rhabdoid tumors, clear cell partially differentiated nephroblastoma, multilocular cystic nephroma, primary renal synovial sarcoma, and anaplastic sarcoma. Nephroblastomatosis of the kidney is a type of nonmalignant neoplasia.[4,5] References
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'By using real medical data concerning nephroblastoma for a single patient in conjunction with plausible values for the model parameters ... based on available literature, a reasonable prediction of the actual tumour volume shrinkage has been made possible,' says Prof. Graf.
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