Literature DB >> 8383281

Position paper: imaging methods for primary renal tumors of childhood: costs versus benefits.

G J D'Angio1, H Rosenberg, K Sharples, P Kelalis, N Breslow, D M Green.   

Abstract

The patterns of disease distribution at diagnosis and during follow-up were cataloged for the primary renal tumors of childhood. These data, derived from more than 1,500 patients, were used to define the most rewarding and cost-effective imaging methods required for patient management. The basic information needed prior to surgery includes whether there is a functioning kidney on the opposite side, and whether there are lung metastases or inferior vena cava thrombi. Simple X-ray examinations and ultrasonography (US) will provide the necessary data. Postoperatively, when the histology is known, examination of the brain (MRI or CT scan) is needed for patients with the rhabdoid tumor and clear cell sarcoma of the kidney (CCSK) who are prone to develop brain lesions; and the skeletal system (bone scan, X-ray skeletal survey) for CCSK and for renal cell carcinoma patients who tend to develop bone metastases. Continuing examination of the lung (chest films) is required for all histologies except perhaps for mesoblastic nephroma, which seldom metastasizes. The opposite kidney needs follow-up (US) for 5 or more years to exclude metachronous involvement if nephrogenic rests are present in either kidney. Sophisticated imaging studies, which cost five times or more than simple X-ray examinations or US, are not warranted routinely, and should be reserved for those cases where simpler, less expensive studies do not suffice for reaching patient management decisions.

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Mesh:

Year:  1993        PMID: 8383281     DOI: 10.1002/mpo.2950210310

Source DB:  PubMed          Journal:  Med Pediatr Oncol        ISSN: 0098-1532


  8 in total

1.  Tumor imaging protocols: problems and challenges.

Authors:  Mervyn D Cohen
Journal:  Pediatr Radiol       Date:  2003-07-10

Review 2.  Staging of common paediatric tumours.

Authors:  Hervé J Brisse
Journal:  Pediatr Radiol       Date:  2009-06

3.  Commentary: imaging and staging of Wilms' tumors: problems and controversies.

Authors:  M D Cohen
Journal:  Pediatr Radiol       Date:  1996

4.  Subsets of very low risk Wilms tumor show distinctive gene expression, histologic, and clinical features.

Authors:  Simone T Sredni; Samantha Gadd; Chiang-Ching Huang; Norman Breslow; Paul Grundy; Daniel M Green; Jeffrey S Dome; Robert C Shamberger; J Bruce Beckwith; Elizabeth J Perlman
Journal:  Clin Cancer Res       Date:  2009-11-10       Impact factor: 12.531

5.  Management and outcome of inoperable Wilms tumor. A report of National Wilms Tumor Study-3.

Authors:  M L Ritchey; K C Pringle; N E Breslow; J Takashima; J Moksness; C W Zuppan; J B Beckwith; P R Thomas; P P Kelalis
Journal:  Ann Surg       Date:  1994-11       Impact factor: 12.969

Review 6.  Imaging in unilateral Wilms tumour.

Authors:  Hervé J Brisse; Anne M Smets; Sue C Kaste; Catherine M Owens
Journal:  Pediatr Radiol       Date:  2007-11-16

Review 7.  Wilms tumour: diagnosis and treatment.

Authors:  M J Coppes; J E Wolff; M L Ritchey
Journal:  Paediatr Drugs       Date:  1999 Oct-Dec       Impact factor: 3.930

Review 8.  Many faces of Wilms Tumor: Recent advances and future directions.

Authors:  Namita Bhutani; Pradeep Kajal; Urvashi Sharma
Journal:  Ann Med Surg (Lond)       Date:  2021-03-07
  8 in total

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