Editorial Comment on “Zinner Syndrome Presenting With Chronic Pelvic Pain and Ejaculatory Dysfunction” From Dr. Sourav and Dr. Tweheyo

Q4 Medicine
Sourav Sudan, Tweheyo Ronald
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引用次数: 0

Abstract

We read with great interest the case report by Patil et al., and this instructive case of Zinner syndrome thoughtfully navigates the diagnostic pathway using magnetic resonance imaging (MRI) to delineate anatomical anomalies [1]; however, it also opens the door for deeper reflection on emerging embryological correlations. While the authors appropriately attributed the pathology to mesonephric duct maldevelopment, the literature now suggests that coexisting anomalies such as Müllerian duct remnants or aberrant mesonephric-Müllerian fusion defects may occasionally coexist in patients with cysts exceeding 2.5 cm [2, 3]. The cyst dimensions in this case could serve as an opportunity to consider subtle embryological overlaps, which may have functional implications.

Furthermore, the report offers an excellent depiction of structural anomalies; however, functional correlates remain an evolving area in such syndromes. For instance, compensatory hyperfunction of the solitary kidney, often seen in unilateral renal agenesis, might benefit from noninvasive evaluation using serum cystatin C or differential renal scintigraphy, which are increasingly being adopted in urological surveillance [4].

Additionally, while semen analysis revealing oligospermia adds an important reproductive dimension, future case discussions should consider incorporating baseline endocrine profiles and scrotal ultrasonography to offer a more holistic reproductive assessment. Such adjuncts, when included, can inform long-term fertility planning and personalize follow-up decisions. This case adds meaningful value to the literature and invites further exploration of how structural clarity can be enriched by functional parameters, especially in a condition where both fertility and renal preservation are central to patient outcomes.

The authors have nothing to report.

The authors have nothing to report.

The authors declare no conflicts of interest.

Sourav博士和Tweheyo博士对“Zinner综合征表现为慢性盆腔疼痛和射精功能障碍”的评论
我们怀着极大的兴趣阅读了Patil等人的病例报告,这一具有指导意义的Zinner综合征病例巧妙地引导了使用磁共振成像(MRI)描绘解剖异常的诊断途径。然而,它也为更深入地思考新兴的胚胎学相关性打开了大门。虽然作者适当地将病理归因于中肾管发育不良,但现在的文献表明,在囊肿超过2.5 cm的患者中,共存的异常,如腰勒氏管残余或异常的中肾-腰勒氏管融合缺陷可能偶尔共存[2,3]。在这种情况下,囊肿的大小可以作为考虑微妙的胚胎学重叠的机会,这可能具有功能意义。此外,该报告还提供了对构造异常的出色描述;然而,在这些综合征中,功能相关性仍然是一个不断发展的领域。例如,单侧肾脏发育不全常出现的单侧肾脏代偿性功能亢进,可能得益于血清胱抑素C或鉴别肾显像的无创评估,这两种方法越来越多地被用于泌尿系统监测[10]。此外,虽然精液分析显示少精症增加了重要的生殖维度,但未来的病例讨论应考虑结合基线内分泌谱和阴囊超声检查,以提供更全面的生殖评估。这些辅助因素,如果包括在内,可以为长期生育计划和个性化后续决定提供信息。该病例为文献增加了有意义的价值,并邀请进一步探索如何通过功能参数丰富结构清晰度,特别是在生育能力和肾脏保存对患者预后至关重要的情况下。作者没有什么可报告的。作者没有什么可报告的。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IJU Case Reports
IJU Case Reports Medicine-Urology
CiteScore
0.60
自引率
0.00%
发文量
147
审稿时长
15 weeks
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