Neoplasia Endocrina múltiple, una Revisión y Actualización de tema sobre una Entidad de Diagnóstico y Manejo Complejo

Palabras clave: neoplasia endocrina múltiple, genética, manejo multidisciplinario

Resumen

Los síndromes de neoplasia endocrina múltiple (NEM) incluyen NEM1, NEM2 (anteriormente NEM2A), NEM3 (anteriormente NEM2B) y el recientemente identificado NEM4. Las presentaciones clínicas son variadas y a menudo se relacionan con la sobreproducción de hormonas específicas. Comprender la genética de cada síndrome ayuda a determinar los plazos de detección. Los tratamientos para cada manifestación dependen de la ubicación, el riesgo de recurrencia o malignidad, el exceso de hormonas y la morbilidad quirúrgica. El manejo multidisciplinario debe incluir genetistas, asesores genéticos, endocrinólogos y cirujanos en patologías endocrinas.

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Publicado
2024-12-30
Cómo citar
Velásquez Quiroga, M. A., Ballesteros López, C. C., Puerta Medina, M. A., Vasquez Castro, J. F., Barón Martínez, J. M., Robles Cuello , N. S., Sierra Cedeño , J. S., Vargas , V. E., & Pérez Ardila, L. J. (2024). Neoplasia Endocrina múltiple, una Revisión y Actualización de tema sobre una Entidad de Diagnóstico y Manejo Complejo. Ciencia Latina Revista Científica Multidisciplinar, 8(6), 4856-4869. https://doi.org/10.37811/cl_rcm.v8i6.15207
Sección
Ciencias de la Salud

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