2018, Número 4
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Med Int Mex 2018; 34 (4)
Dosis atípica de bevacizumab en un paciente con síndrome de Osler-Weber-Rendu
Estrada-Martínez LE, López-Rodríguez WE, García-Ortega GN, Iturbide-Escamilla AE, Chapuli-Azcatl FJ
Idioma: Español
Referencias bibliográficas: 23
Paginas: 649-657
Archivo PDF: 347.06 Kb.
RESUMEN
El síndrome de Osler-Weber-Rendu es una enfermedad de transmisión autosómica
dominante. Si bien el síntoma más común es la epistaxis, existen muchas alteraciones
viscerales que deben considerarse al momento del estudio. Los anti-VEFG son un
pilar en el tratamiento, aunque no existe consenso acerca de la dosis a administrar.
Comunicamos el caso de un paciente con síndrome de Osler-Weber-Rendu atendido
en el servicio de Medicina Interna del Hospital Regional de Puebla, al que se prescribió
una dosis atípica de bevacizumab con buena respuesta terapéutica.
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