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VII

Radiol Bras. 2014 Jan/Fev;47(1):VII

Wilms’ tumor is the malignant abdominal tumor most commonly found in children, with a prevalence of one case per 1000 inhabitants(1). This tumor may be hereditary or

spo-radic in nature, and has a renal origin, although rarely may be extrarenal. It may be multifocal, uni- or bilateral. The most clinical presentation is the presence of an asymptomatic abdominal mass of insidious growth. Secondary arterial hy-pertension may be observed in up to 25% of the patients, as a result from increased rennin levels.

Currently, therapeutic advances have allowed a success-ful treatment of such tumors in approximately 90% of cases(2). Over the last 30 years, the significant improvement

in the prognosis has occurred particularly because of innu-merable randomized, multicentric trials in association with a multidisciplinary management to improve the outcomes in cases of children’s cancer(3). One of the main contributing

factors for an earlier diagnosis and for a more accurate stag-ing has been the aid provided by imagstag-ing methods, such as computed tomography (CT), Doppler ultrasonography (US) and magnetic resonance imaging (MRI).

The main objectives of imaging methods in Wilms’ tu-mor staging are the following: 1) to identify the tutu-mor origin; 2) to evaluate the tumor extent; 3) to evaluate the involve-ment of the renal vascular pedicle; 4) to detect regional lymph node metastasis; 5) to detect the presence of bilateral Wilms’ tumors; 6) to detect the presence of distant metasta-sis.

Specifically in relation to lymph nodes involvement, pre-vious studies have demonstrated that CT presents low speci-ficity and low positive predictive value in the identification of metastatic lymph node involvement, which affects the stag-ing and, consequently, the therapeutic approach(4,5). In the

present issue of Radiologia Brasileira the reader will find an interesting study presented by Silva et al.(6) approaching

the local staging of Wilms’ tumor by CT as well as its accu-racy in the detection of lymph node metastasis. In such a study, the authors conclude that CT has low specificity and low positive predictive value in the detection of metastasis.

0100-3984 © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem

Wilms’ tumor: is computed tomography specific to detect

lymph node metastasis?

Tumor de Wilms: a tomografia é específica para detectar metástase linfonodal?

Matteo Baldisserotto1

On the other hand, the absence of visible lymph nodes prac-tically rules out lymph node involvement.

This is due to the fact that the detection of abdominal lymph nodes in both female and male, asymptomatic chil-dren of all ages is a common, nonspecific finding and should be evaluated only in an appropriate clinical context(7). The

identification of abdominal lymph nodes at CT, their dimen-sions and meaning in the pediatric population have been dis-cussed by several studies. Lymph nodes measuring 5–10 mm in their smallest diameter are frequently found at abdomi-nal CT in healthy children(8).

The use of FDG-PET does not add any information to conventional CT in the staging of patients with Wilms’ tumor, in the evaluation of their response to preoperative chemo-therapy as well as in their clinical follow-up(9). Such method is useful to rule out the presence of residual disease once a first-line treatment is completed and in the pretherapeutic staging in cases of disease recurrence. Additionally, it seems that there is a good correlation between the standard up-take value and histological differentiation(9).

Finally, in the investigation of pediatric patients with Wilms’ tumor, the radiologist must be attentive to the fact that lymph nodes detected at imaging studies do not corre-spond to metastatic lymph node involvement. In the cases where abdominal lymph nodes are not identified, metastatic lymph node involvement is improbable.

REFERENCES

1. Dähnert WF. Radiology review manual. 6th ed. Philadelphia: Lippincott Williams & Wilkins; 2007. p. 992–3.

2. Pritchard-Jones K. Controversies and advances in the management of Wilms’ tu-mour. Arch Dis Child. 2002;87:241–4.

3. Davidoff AM. Wilms tumor. Curr Opin Pediatr. 2009;21:357–64.

4. Gow KW, Roberts IF, Jamieson DH, et al. Local staging of Wilms’tumor – comput-erized tomography correlation with histological findings. J Pediatr Surg. 2000;35: 677–9.

5. Ng YY, Hall-Craggs MA, Dicks-Mireaux C, et al. Wilms’ tumour: pre- and post-che-motherapy CT appearances. Clin Radiol. 1991;43:255–9.

6. Silva EJC, Silva GAP. Comportamento local e metástases linfonodais do tumor de Wilms: acurácia da tomografia computadorizada. Radiol Bras. 2014;47:9–13. 7. McDonald K, Duffy P, Chowdhury T, et al. Added value of abdominal

cross-sec-tional imaging (CT or MRI) in staging of Wilms’ tumours. Clin Radiol. 2013;68:16– 20.

8. Karmazyn B, Werner EA, Rejaie B, et al. Mesenteric lymph nodes in children: what is normal? Pediatr Radiol. 2005;35:774–7.

9. Misch D, Steffen IG, Schönberger S, et al. Use of positron emission tomography for staging, preoperative response assessment and posttherapeutic evaluation in children with Wilms tumour. Eur J Nucl Med Mol Imaging. 2008;35:1642–50.

1. Coordinator for the Imaging Center at Instituto do Cérebro do Rio Grande do Sul, Professor (Graduation and Post-graduation), School of Medicine, Pontifícia Uni-versidade Católica do Rio Grande do Sul (PUCRS), Associate Professor, UniUni-versidade Federal das Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil. E-mail: matteo.baldisserotto@pucrs.br.

Referências

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