Arellano BRH, Torres VA, García UC, Domínguez MA

Idioma: Español
Referencias bibliográficas: 18
Paginas: 399-403
Archivo PDF: 240.51 Kb.

RESUMEN

El tumor carcinoide de ovario es raro (1%); es una neoplasia de crecimiento lento, por lo general bien diferenciada, que puede permanecer sin diagnóstico durante meses o años antes de dar metástasis. La complicación más grave de este tumor es la crisis carcinoide. El diagnóstico se realiza con marcadores tumorales que incluyen: enolasa neuronal específica, cromogranina A, serotonina sérica y 5 H-hidroxiindolacético. El tratamiento es con octreotida. Cuando la crisis no se diagnostica y trata oportunamente, la mortalidad es alta. Se describe el caso de una paciente de 59 años de edad, con manifestaciones floridas del síndrome carcinoide, incluida la afección cardiaca y la insuficiencia renal.

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