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Vol. 12. Issue 3.
Pages 253 (January 2001)
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Vol. 12. Issue 3.
Pages 253 (January 2001)
12. Plasmocitoma intracraneal solitario
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H. Sandoval, W. Egas, I. Jorge, F. Robaina
Hospital General de Gran Canaria Dr. Negrín
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Los tumores de células plasmáticas pueden manifestarse como tres entidades patológicas: a) mieloma múltiple; b) plasmocitoma solitario óseo; o c) plasmocitoma extramedular. La presencia de plasmocitomas intracraneales durales solitarios es conocida en la literatura fundamentalmente por publicación de casos. Se trata de tumores raros cuya imagen radiológica es poco característica, dando lugar a un subdiagnóstico o interpretación errónea como meningioma. En los casos de lesión solitaria en que no haya mieloma múltiple, la resección quirúrgica completa y radioterapia subsecuente redundan en buen pronóstico a largo plazo. Los autores presentan un caso de plasmocitoma solitario dural de ala mayor de esfenoides izquierdo con restricción policlonal IGa-g lambda y hacen una revisión de la literatura.

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