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Tumor de Wilms en paciente adulto. Presentación de un caso / Wilms tumor in an adult patient: case report
Martínez Mansur, Rodrigo; Piana, Mauro; Codone, José; Díez, Marcos; Elizalde, Florencia; Reyes, Eduardo; Villeta, Matias; Lioy Lupis, Marcelo; Solano, Francisco; Serrano, A; Proto, J; Sicher, R.
Affiliation
  • Martínez Mansur, Rodrigo; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Piana, Mauro; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Codone, José; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Díez, Marcos; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Elizalde, Florencia; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Reyes, Eduardo; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Villeta, Matias; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Lioy Lupis, Marcelo; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Solano, Francisco; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Serrano, A; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Proto, J; Hospital Cosme Argerich. Buenos Aires. Argentina
  • Sicher, R; Hospital Cosme Argerich. Buenos Aires. Argentina
Arch. esp. urol. (Ed. impr.) ; 59(6): 632-634, jul.-ago. 2006. ilus
Article in Es | IBECS | ID: ibc-049359
Responsible library: ES1.1
Localization: ES1.1 - BNCS
RESUMEN
El nefroblastoma o tumor de Wilms, es la neoplasia renal más común en niños y representa actualmente la quinta parte en tumor malignos en este grupo. Sin embargo la incidencia de dicho tumor en el adulto es mucho más rara con tan sólo menos de 250 casos reportados en la literatura. Debido a la baja frecuencia de esta patología en adultos no existe una modalidad en el tratamiento aceptada mundialmente. Actualmente las opciones terapéuticas se desprenden del National Wilms Tumor Study (NTWS). Presentamos a continuación un nuevo caso con las imágenes radiográficas, hallazgos histológicos, evolución y seguimiento
ABSTRACT
Nephroblastoma or Wilms tumor is the most common renal neoplasia in children, representing 1/5 of the malignant tumors in this group. Nevertheless, the incidence of such tumor in adults is much rarer with less than 250 cases reported. Due to the low-frequency of this pathology in adults there is not a world widely accepted treatment modality. Currently, the therapeutic options derive from the National Wilms Tumor Study (NWTS). We report a new case with the radiological images, histologic findings, outcomes and follow-up
Subject(s)
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Wilms Tumor / Kidney Neoplasms Limits: Humans / Male Language: Spanish Journal: Arch. esp. urol. (Ed. impr.) Year: 2006 Document type: Article Institution/Affiliation country: Hospital Cosme Argerich/Argentina
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Wilms Tumor / Kidney Neoplasms Limits: Humans / Male Language: Spanish Journal: Arch. esp. urol. (Ed. impr.) Year: 2006 Document type: Article Institution/Affiliation country: Hospital Cosme Argerich/Argentina
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