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Zinner Syndrome in Pediatric Age: Issues in the Diagnosis and Treatment of a Rare Malformation Complex

机译:小儿锌氏综合症:罕见畸形综合症的诊断和治疗问题

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摘要

Zinner syndrome (ZS) is the association of congenital seminal vesicle cysts and ipsilateral upper urinary tract anomalies, such as multicystic displastic kidney (MCDK). This condition is rare in pediatric age and both diagnosis and treatment are challenging. The aim of this study was to analyze the issues in diagnosis, management, and treatment of ZS in pediatric age. The medical records of two patients with ZS were examined. Furthermore, a review of the literature on this topic in pediatric age was performed. In our experience the diagnosis of ZS was incidentally achieved in the first months of life, as a consequence of studies performed for a prenatal diagnosis of MCDK. The first patient presented unspecific and transient symptoms, the second infant was completely asymptomatic. They were conservatively treated, with a long-term follow-up planned at least until adolescence. Fifty cases of ZS in pediatric age have been reported in the literature up to now. Only 12/50 were diagnosed in the first year of life. The diagnosis was demanding, as the clinical presentation was unspecific and the results at imaging studies needed a differential diagnosis with other retrovesical masses. More than 80% of these cases were asymptomatic at long-term follow-up. Therefore, a conservative management of ZS has been accepted for asymptomatic or poorly symptomatic patients, with occasional, transient, and unspecific symptoms, such as urinary tract infections or orchyepididimytis. As the surgical management is challenging, it is proposed only in those symptomatic patients. In conclusion, ZS is rare in pediatric age. However, it should be considered in the differential diagnosis of cystic masses within the pelvis in males with ipsilateral renal anomalies. A conservative treatment with a long-term follow-up is a safe option in the management of asymptomatic or poorly symptomatic patients, thus reserving the surgical approach only in those cases with symptoms.
机译:Zinner综合征(ZS)是先天性精囊囊肿与同侧上尿路异常(如多囊性增生性肾脏病(MCDK))的关联。这种情况在儿科年龄很少见,诊断和治疗均具有挑战性。这项研究的目的是分析在小儿期ZS的诊断,管理和治疗方面的问题。检查了两名ZS患者的病历。此外,对儿童年龄这一主题的文献进行了回顾。根据我们的经验,由于进行了MCDK产前诊断的研究,偶然地在生命的最初几个月实现了ZS的诊断。第一名患者表现出非特异性和暂时性症状,第二名婴儿完全无症状。对他们进行了保守治疗,并计划至少在青春期之前进行长期随访。迄今为止,已有文献报道了50例小儿ZS病例。生命的第一年仅被诊断出12/50。诊断要求很高,因为临床表现不明确,影像学研究的结果需要与其他膀胱后部肿块进行鉴别诊断。这些病例中超过80%在长期随访中无症状。因此,无症状或症状较轻的患者,偶发性,短暂性和非特异性症状,例如尿路感染或链霉菌病,已接受保守治疗。由于手术处理具有挑战性,因此仅在那些有症状的患者中提出。总而言之,ZS在儿童年龄中很少见。但是,在具有同侧肾脏异常的男性中,在盆腔内囊性肿块的鉴别诊断中应考虑这一点。在无症状或症状较轻的患者中,采用长期随访的保守治疗是一种安全的选择,因此仅在出现症状的情况下才保留手术方法。

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