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Revista Mexicana de Urología

Organo Oficial de la Sociedad Mexicana de Urología
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2010, Number 6

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Rev Mex Urol 2010; 70 (6)

Adenocarcinoma renal atípico en paciente adolescente; informe de un caso y revisión de la bibliografía

Landa-Soler M, Figueroa-Zarza M, Cruz-García VP
Full text How to cite this article

Language: Spanish
References: 10
Page: 389-393
PDF size: 1459.78 Kb.


Key words:

Kidney tumor, papillary renal adenocarcinoma, Mexico.

ABSTRACT

Introduction: Renal tumors present more frequently in adult patients and clear cell adenocarcinoma is the most frequent. Symptoms include pain, hematuria, and palpable mass in up to fifteen per cent of cases.
Objective: To present the case of an adolescent patient with histologically rare renal tumor.
Methods: Patient is a seventeen-year-old young man who presented with pain in left costovertebral angle and macroscopic hematuria. Physical examination revealed positive left costovertebral angle percussion. Diagnosis was made with kidney ultrasound and computed axial tomography.
Results: Left radical nephrectomy was performed. Histopathological study reported papillary adenocarcinoma of the kidney with microscopic clear cell component and tumor-free margins.
Discussion: Papillary kidney tumors are rare in the adolescent. In the present case computed axial tomography and radiological studies revealed the presence of kidney tumor, and radical nephrectomy was indicated.
Conclusions: Kidney tumors do not present frequently in adolescence. It is important to carry out adequate study protocol in order to make opportune diagnosis and thus determine adequate treatment for these patients.


REFERENCES

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  2. Magnani C, Gatta G, Corazziari I, et al. Childhood malignancies in the EUROCARE study: the database and the methods of survival analysis. Eur J Cancer 2001;37:678-86.

  3. Ornstein D, Lubensky I, et al. Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer. J Urol 2000;163:431-3.

  4. Zbar B, Glenn G, Lubensky I, et al. Hereditary papillary renal cell carcinoma: clinical studies in 10 families. J Urol 1995;153(3 Pt 2):907-12.

  5. Zbar B, Tory K, Merino M, et al. Hereditary papillary renal cell carcinoma. J Urol 1994;151:561-6.

  6. McClellan W, Choyke P, et al. Renal cancer in families with hereditary renal cancer: prospective analysis of a tumor size thereshold for renal parenchymal sparing surgery. J Urol 1999;161:1475-9.

  7. Eun-Jung J, Ju Lee H, et al. Young age is independent prognostic factor for cancer-specific survival of low-stage clear cell renal cell carcinoma. Urology 2009;73:137-41.

  8. Gillett MD, Cheville JC, et al. Comparision of presentation and outcome for patients 18 to 40 an 60 to 70 years old with solid renal masses. J Urol 2005;173:1893-6.

  9. Schiff M, Herter G, Lytton B. Renal adenocarcinoma in young adults. Urology 1985;25:357-9.

  10. Solomon D, Schwartz A. Renal pathology in von Hippel-Lindau disease. Hum Pathol 1988;19:1072-9.




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Rev Mex Urol. 2010;70