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Primary Ewing´s sarcoma/primitive neuroectodermal tumor of the kidney. An infrequent finding / Sarcoma de Ewing primario/Tumor neuroectodérmico primitivo renal. Un hallazgo infrecuente
David Parada, David; Godoy, Alí; Liuzzi, Francisco; Peña, Karla B; Romero, Aramis; Parada, Arelí M.
Affiliation
  • David Parada, David; Central University of Venezuela. School of Medicine, “José María Vargas”. Vargas Hospital. Caracas. Venezuela
  • Godoy, Alí; Vargas Hospital. Caracas. Venezuela
  • Liuzzi, Francisco; Vargas Hospital. Caracas. Venezuela
  • Peña, Karla B; Vargas Hospital. Caracas. Venezuela
  • Romero, Aramis; Vargas Hospital. Caracas. Venezuela
  • Parada, Arelí M; Central University of Venezuela. School of Medicine, “José María Vargas”. Caracas. Venezuela
Arch. esp. urol. (Ed. impr.) ; 60(3): 321-325, abr. 2007. ilus, tab
Article in En | IBECS | ID: ibc-055393
Responsible library: ES1.1
Localization: ES1.1 - BNCS
ABSTRACT
Objetive Ewing's sarcoma/Primitive neuroectodermal tumor (ES/PNET) is an extraordinarily rare primary tumor in the kidney. We report herein the clinical, histological, and immunohisto-chemical features of a primary renal ES/PNET.

Methods:

A 19-year old male referred a two weeks history of constant, colic, left flank pain, and fever. A left radical nephrectomy was performed. Gross pathologic examination showed pink-tan, lobulated solid tumor, localized at the superior pole.

Results:

Histologically, the tumor was solid with necrosis. The neoplastic cells showed a small amount of clear cytoplasm, and had vesicular nuclei with small nucleoli. Immunohistochemical studies showed strongly and diffusely positive staining for CD99 in a membranous pattern.

Conclusions:

This case represents a typical ES/PNET, affecting a young male patient. Adequate diagnosis is important because this neoplasm has an aggressive behaviour (AU)
RESUMEN
El sarcoma de Ewing/Tumor Neuroectodermico Primitivo (SE/TNEP) del riñón es una neoplasia extremadamente rara en el riñón. Presentamos los hallazgos clínicos, histológicos e inmunohistoquímicos de un SE/TNEP primario renal.

Métodos:

Un paciente varón de 19 años refirió historia de dos semanas de dolor tipo cólico, constante, en el flanco izquierdo y fiebre. Se hizo nefrectomía radical izquierda. El examen macroscópico mostró un tumor sólido, lobulado, pardo-rosado, localizado en el polo superior.

Resultados:

Histológicamente el tumor era sólido con necrosis. Las células neoplásicas mostraron citoplasma escaso claro y poseían un núcleo vesicular con nucléolo pequeño. Los estudios inmunohistoquímicos mostraron una fuerte y difusa positividad para el CD99 en un patrón membranoso.

Conclusiones:

Este caso representa un típico SE/TNEP, afectando a un varón joven. Es importante un diagnóstico adecuado debido a que esta neoplasia tiene una conducta agresiva (AU)
Subject(s)
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Sarcoma, Ewing / Immunohistochemistry / Tomography, Emission-Computed / Neuroectodermal Tumors, Primitive, Peripheral / Nephrectomy Type of study: Diagnostic study Limits: Adult / Humans / Male Language: English Journal: Arch. esp. urol. (Ed. impr.) Year: 2007 Document type: Article Institution/Affiliation country: Central University of Venezuela/Venezuela / Vargas Hospital/Venezuela
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Sarcoma, Ewing / Immunohistochemistry / Tomography, Emission-Computed / Neuroectodermal Tumors, Primitive, Peripheral / Nephrectomy Type of study: Diagnostic study Limits: Adult / Humans / Male Language: English Journal: Arch. esp. urol. (Ed. impr.) Year: 2007 Document type: Article Institution/Affiliation country: Central University of Venezuela/Venezuela / Vargas Hospital/Venezuela
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