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鞘内注射治疗脑室内-腹腔分流术后阴囊迁移:病例报告及 48 例系统回顾。

Treatment Options for Scrotal Migration of Ventriculoperitoneal Shunts: Case Illustration and Systematic Review of 48 Cases.

机构信息

Department of Neurosurgery, Kepler University Hospital, Neuromedcampus, Linz, Austria.

Johannes Kepler University (JKU), Linz, Austria.

出版信息

Oper Neurosurg (Hagerstown). 2021 Aug 16;21(3):87-93. doi: 10.1093/ons/opab152.

Abstract

BACKGROUND

Scrotal migration of intact or disconnected tubing is a rare complication of ventriculoperitoneal shunts. While some illustrative case reports can be found in the literature, a systematic review on treatment options is lacking.

OBJECTIVE

To propose the first literature-based treatment algorithm on scrotal shunt migration.

METHODS

We conducted a literature search using the keywords: "VP," "ventriculoperitoneal," "shunt," and "scrotum." We identified 36 publications with 48 cases reported including our index case.

RESULTS

Median age at presentation was 13.5 mo (3 d to 65 yr) which was 4 mo (3 d to 72 mo) after last shunt-related surgery. All patients had scrotal swelling, 39 (81%) patients presented without other symptoms, 4 (8%) had additionally local pain, and 4 (8%) patients presented with symptoms of shunt dysfunction. Treatment was surgically in all but one case where spontaneous resolution without repeat migration occurred. In 3 of 4 patients who had either subcutaneous shortening or abdominal repositioning of the shunt without hernia repair, scrotal shunt migration recurred within the following month. Whereas the surgical treatment with reposition of the migrated catheter back into the peritoneal cavity via a groin incision plus hernia repair yielded a definite treatment in all 26 performed cases, the revision rate was significantly higher in the shunt revision without hernia repair cohort (P = .0009).

CONCLUSION

Scrotal shunt migration is a rare shunt complication with good recovery when treated surgically. We recommend hernia repair in addition to either manual or surgical repositioning of migrated tubing.

摘要

背景

完整或断开的管的鞘膜内迁移是脑室腹腔分流术的罕见并发症。虽然文献中有一些说明性病例报告,但缺乏关于治疗选择的系统评价。

目的

提出鞘膜内分流迁移的首个基于文献的治疗算法。

方法

我们使用关键词“VP”、“ventriculoperitoneal”、“shunt”和“scrotum”进行了文献检索。我们确定了 36 篇出版物,其中包括我们的索引病例,共报告了 48 例病例。

结果

中位就诊年龄为 13.5 个月(3 天至 65 岁),为最后一次分流相关手术后 4 个月(3 天至 72 个月)。所有患者均有阴囊肿胀,39 例(81%)患者无其他症状,4 例(8%)患者伴有局部疼痛,4 例(8%)患者出现分流功能障碍症状。除 1 例外,所有患者均接受手术治疗,该患者未再次出现迁移且无需再次手术。在 3 例接受皮下缩短或腹部重新定位分流而未修复疝的患者中,鞘膜内分流迁移在接下来的 1 个月内再次发生。而通过腹股沟切口将迁移的导管重新置于腹膜腔并修复疝的手术治疗在 26 例进行的病例中取得了明确的治疗效果,未修复疝的分流修复组的翻修率明显更高(P=0.0009)。

结论

鞘膜内分流迁移是一种罕见的分流并发症,通过手术治疗可获得良好的恢复。我们建议在手动或手术重新定位迁移的导管的同时进行疝修复。

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