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Organo Oficial de la Sociedad Mexicana de Urología

2024, Número 1

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Rev Mex Urol 2024; 84 (1)


Revisión sistemática del síndrome de Zinner

Palacios-Rosas E, Torres-Razo A, Enríquez-González EA

Idioma: Español
Referencias bibliográficas: 40
Paginas: 1-10
Archivo PDF: 251.76 Kb.


RESUMEN

El síndrome de Zinner se caracteriza por ser una patología de origen congénito en la cual se observa una ausencia unilateral del riñón, presencia de quistes y obstrucción en los conductos eyaculatorios. Al ser diagnosticada en la etapa de actividad sexual de los pacientes, puede causar problemas en la sexualidad o en la reproductividad de la persona. Este trabajo tuvo como objetivo realizar una revisión sistemática de casos clínicos reportados en la literatura entre el año 2013 a 2023. Se evaluaron 42 reportes de casos clínicos con dicho síndrome, con un total de 49 pacientes con una media de edad de 22.5 años, el 77.55 % de los pacientes presentaron quistes, ausencia del riñón derecho en el 44.90% de los pacientes, y el 91.84 % presentaron dolor. El tratamiento más común para esta patología es la laparoscopia (16.33 %) y en los casos revisados no se presentaron complicaciones ni decesos. El identificar las diferentes presentaciones de este síndrome podría mejorar la rapidez del diagnóstico, y garantizar un manejo efectivo, mejorando con ello la calidad de vida de los pacientes.


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