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儿童期的齐纳综合征:一种罕见畸形综合征的诊断与治疗问题

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

作者信息

Cascini Valentina, Di Renzo Dacia, Guerriero Vittorio, Lauriti Giuseppe, Lelli Chiesa Pierluigi

机构信息

Department of Pediatric Surgery, Spirito Santo Hospital of Pescara, G. D'Annunzio University of Chieti-Pescara, Chieti, Italy.

Department of Medicine and Aging Sciences, G. D'Annunzio University of Chieti-Pescara, Chieti, Italy.

出版信息

Front Pediatr. 2019 Apr 9;7:129. doi: 10.3389/fped.2019.00129. eCollection 2019.

Abstract

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.

摘要

津纳综合征(ZS)是先天性精囊囊肿与同侧上尿路异常(如多囊性发育不良肾[MCDK])的联合病症。这种情况在儿童期较为罕见,诊断和治疗都具有挑战性。本研究的目的是分析儿童期ZS在诊断、管理和治疗方面的问题。我们检查了两名ZS患者的病历。此外,还对儿童期关于该主题的文献进行了综述。根据我们的经验,ZS的诊断在生命的最初几个月偶然达成,这是对MCDK进行产前诊断所做研究的结果。第一名患者出现非特异性和短暂性症状,第二名婴儿则完全无症状。他们接受了保守治疗,并计划进行至少直至青春期的长期随访。到目前为止,文献中已报道了50例儿童期ZS病例。其中只有12/50在出生后第一年被诊断出来。诊断颇具难度,因为临床表现不具特异性,影像学检查结果需要与其他膀胱后肿块进行鉴别诊断。这些病例中超过80%在长期随访中无症状。因此,对于无症状或症状轻微、仅有偶尔、短暂且非特异性症状(如尿路感染或附睾炎)的ZS患者,已接受保守治疗。由于手术管理具有挑战性,仅对那些有症状的患者建议采用手术治疗。总之,ZS在儿童期较为罕见。然而,在对伴有同侧肾异常的男性盆腔内囊性肿块进行鉴别诊断时应考虑到它。对于无症状或症状轻微的患者,采用长期随访的保守治疗是一种安全的选择,从而仅对那些有症状的病例采用手术方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4a/6465625/d8266635c00e/fped-07-00129-g0001.jpg

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