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Carcinoma corticosuprarrenal - Treatment

Nombres alternativos

Tumor suprarrenal

Tratamiento:

El tratamiento primario es la extirpación quirúrgica del tumor. Es posible que el carcinoma corticosuprarrenal no responda bien a la quimioterapia. Se pueden administrar medicamentos para disminuir la producción de cortisol, que causa muchos de los síntomas.

Expectativas (pronóstico):

El pronóstico depende de qué tan pronto se efectúe el diagnóstico y de si el tumor se ha diseminado (hecho metástasis) o no. Los tumores que se han diseminado generalmente llevan a la muerte en cuestión de 1 a 3 años.

Complicaciones:

El tumor se puede diseminar al hígado, al hueso, al pulmón o a otras áreas.

Situaciones que requieren asistencia médica:

Consulte con el médico si usted o su hijo presenta síntomas de carcinoma corticosuprarrenal, síndrome de Cushing o insuficiencia en el crecimiento.

  • Reviewed last on: 8/14/2010
  • David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

Referencias

Lal G, O’Dorisio T, McDougall R, Weigel RJ. Cancer of the endocrine system. In: Abeloff MD, Armitage JO, Niederhuber JE, Kastan MB, McKenna WG, eds. Clinical Oncology. 4th ed. Philadelphia, Pa: Elsevier Churchill Livingstone; 2008:chap 75.

National Cancer Institute. Adrenocortical carcinoma treatment PDQ. Updated May 16, 2008.

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