Estrategias terapéuticas de aneurisma abdominal en síndrome de Marfan a propósito de un caso.
Abstract
Se presenta el caso de una paciente que acude a consulta externa del Hospital Vicente Corral Moscoso con diagnóstico de aneurisma de aorta abdominal realizado mediante tomografía, además se observa que la paciente presenta un biotipo compatible con Síndrome de Marfan lo que constituye un desafío diagnóstico y terapéutico. El Síndrome de Marfan se presenta en 1 a 3 casos en cada 10.000 pacientes y es causado por defectos en un gen lla- mado fibrilina-1, el cual juega un papel importante para la síntesis del tejido conectivo del cuerpo además de acompañarse de mal formaciones car- diacas y vasculares.
DeCS: miotomía extendida, acalasia, funduplicatura, cirugía mínimamente invasiva.
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