2024, Number 1
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Rev Mex Urol 2024; 84 (1)
Systematic review of Zinner syndrome
Palacios-Rosas E, Torres-Razo A, Enríquez-González EA
Language: Spanish
References: 40
Page: 1-10
PDF size: 251.76 Kb.
ABSTRACT
Zinner syndrome is characterized as a pathology of congenital
origin in which there is a unilateral absence of the
kidney, presence of cysts and obstruction in the ejaculatory
ducts. Being diagnosed in the stage of sexual activity of patients,
it can cause problems in the person’s sexuality or
reproduction. The objective of this work was to carry out a
systematic review of clinical cases reported in the literature
between 2013 and 2023. 42 reports of clinical cases with
Zinner syndrome were evaluated, with a total of 49 patients
with a mean age of 22.5 years, the 77.55 % of the patients
presented cysts, absence of the right kidney in 44.90 % of
the patients, and 91.84 % presented pain. The most common
treatment for this pathology was laparoscopy (16.33
%) and in the reviewed cases there were no complications
or deaths. Identifying the different presentations of this syndrome
could improve the speed of diagnosis and guarantee
effective management, thereby improving the quality of
life of patients.
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