El tumor de Wilms también recibe el nombre de nefroblastoma y puede afectar ambos riñones, pero normalmente se presenta sólo en uno. Los médicos creen. Wilm Tumor. Français: Tumeur de Wilms, – Néphroblastome. Deutsch: Nephroblastom, – Wilms-Tumor. Español: Tumor de Wilms, – Nefroblastoma. Português. With the availability of several protocols in the management of Wilms’ tumor, there is dilemma in the minds of the treating oncologists or pediatric onco- surgeons.

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The high success rate is an accomplishment in treatment of Wilms’ nefroblastomw, and it serves as an excellent model and encouragement for treatment of other childhood cancers.

In patients with chronic renal failure caused by bilateral nephrectomy, ongoing treatment with dialysis support can be achieved through the choice of effective drugs and knowledge nefrkblastoma their pharmacokinetics and pharmacodynamics. Hyperechoic areas may represent areas of fat, calcification or haemorrhage. Med Pediatr Oncol, 22pp. Importance of time interval to the development of a second tumor. Other markers which can affect management include chromosomes and nerve receptors.

If this mutates, which can be signalled by abnormal amplification, cancerous cells can develop and the resulting mass is more resistant to treatment, thus it has a more unfavourable outcome [ 1 ].

The heterogeneity of the tumour, and its biological characteristics, mean the prognosis is highly variable at different ages. See more popular or the latest prezis. Nephroblastoma, also more commonly known as a Wilms tumour, is the commonest renal tumour in childhood and more typically presents as abdominal pathology with few constitutional symptoms, although rarely haematuria can be a presenting feature.

In such cases, surgical intervention by a surgeon who is experienced in the removal of such a fragile tumor is imperative.

Accurate staging, especially the presence or absence of nodal disease, is vital in Wilms tumour to ensure appropriate management pathways are adhered to [ 23 ]. Kidney Glandular and epithelial neoplasm: Certainly CT is superior to chest radiography for the detection of small lesions, but these may not always represent metastases. Vascular invasion is not a classic feature demonstrated on cross-sectional imaging [ 2 ].


Most cases do not have mutations in any of these genes. Only comments written in English can be processed. LOH for these chromosomal regions can now be used as an independent prognostic factor together with disease stage to target intensity of treatment to risk of treatment failure.

Some behave aggressively while others, typically in infancy, may spontaneously regress. Neuroblastoma and Wilms tumour are both relatively common abdominal childhood cancers. National Center for Biotechnology InformationU. Presenting features are diverse and very much dependent on the anatomical location of the tumour.

Failure to sample lymph nodes leads to downstaging and under-treatment of the patient. Abstract Neuroblastoma NBL is the most common extra-cranial tumour in childhood. NWTS 3 — To reduce the treatment for low-risk patients and find better chemotherapy for those at high risk for relapse. Synovial sarcoma Clear-cell sarcoma. On MR at diagnosis, the tumour tends to return low signal on T1-weighted sequences with high signal on T2 [ 3 ]. The tumour extent is easily visualised on non-contrast T1W and T2W sequences, but small bilateral tumours and foci of nephroblastomatosis are often best seen after gadolinium administration.

Tumor de Wilms

NWTS 1 — Nefrobalstoma determine the effect of surgical technique on the results of the treatment. The first sign is normally a painless abdominal tumor that can be easily felt by the doctor. The natural histories and typical clinical courses of these common tumours are very different. Staging is based on anatomical findings and tumor cells pathology.

Purpose of study NWTS 1 — To determine the effect of surgical technique on the results of the treatment. In more localised adrenal or other L1 tumours, pre-operative MRI is preferred over CT as no significant vascular encasement is typically present.


Bilateral nephrectomies followed by renal transplant becomes mandatory when bilateral partial nephrectomies, unilateral radical nephrectomy with opposite partial nephrectomy as renal salvage procedures, or in cases where the tumor does not respond to chemotherapy and salvage of the kidney is not possible. Stage II — For patients with negative lymph nodes, the rate of relapse was reduced by treatment with epirubicin without radiation therapy.

Subsequent to ,[ 1 ] amongst the number of published reports, there was insufficient large series data collection on patients with this tumor. In our Indian circumstances where more than these basic investigations may be difficult to perform, probably it is more appropriate and feasible to follow the SIOP protocol for management of Wilms’ tumor with the added advantage of preventing intra-operative tumor spillage with upfront chemotherapy.

This paper reviews the clinical aspects and imaging characteristics of both tumours, summarising the key differences to aid the paediatrician and radiologist in their diagnosis and management. The MYCN oncogene is responsible for providing the code used by proteins in tissue development. Tumor is limited to the kidney and completely excised a.

Wilms’ tumor – Wikipedia

Wilms’ tumor Synonyms Wilms’ tumor Cut section showing two halves of a nephroblastoma specimen. The promoters of SIOP with a view of reducing the risk of tumor rupture during upfront surgery, as was seen during NWTS studies, planned upfront therapy — initially radiotherapy and later chemotherapy to shrink the tumor. The documents contained in this web site are presented for information purposes only.

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