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首页> 外文期刊>Neuropediatrics >Shunt Dependency Syndrome after Cyst-Peritoneal Shunt Resolved by Keyhole Microsurgical Cyst Resection: Two Case Reports and Literature Review
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Shunt Dependency Syndrome after Cyst-Peritoneal Shunt Resolved by Keyhole Microsurgical Cyst Resection: Two Case Reports and Literature Review

机译:分流依赖性综合征在囊肿分流后通过髓显微外科囊肿切除解决:两种报告和文献综述

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摘要

Objective Shunt dependency syndrome after cyst-peritoneal (CP) shunt is a rare but serious complication which leads to increased intracranial pressure and neurological deficit. The possible mechanism still remains in controversy. We present our experience on the treatment of the complication and attempt to find a better therapy strategy for the complication. Methods Two children with middle fossa arachnoid cysts underwent CP shunt with fixed pressure catheters at an opening pressure of 7 cmH_(2)O and then developed dependency syndrome. Both patients were effectively treated by mini-invasive cyst wall excision with the shunts reserved. The clinical manifestation, radiological findings, treatment methods, and therapeutic outcomes were reviewed retrospectively. Results The time from shunt surgery to shunt dependency syndrome occurrence was 4 and 2 years, respectively. Computed tomography/magnetic resonance findings of the brain showed remarkably collapsed cysts with normal or small ventricles. Both patients underwent secondary mini-invasive cyst wall excision and shunt catheters were reserved. After the operations, their symptoms were resolved except one case with marginally improved visual impairment. Conclusion Shunt dependency syndrome is a rare but dangerous complication of CP shunt and should be treated in time. Collapsed and thickened cyst wall intermittent covering the catheter head end, decreased brain compliance due to chronic fibrosis, as well as regression of cerebrospinal fluid absorption could be the pathogenesis. We suggest keyhole resection of the residual cyst wall as an effective and mini-invasive treatment option.
机译:囊肿腹膜(CP)分流后的客观分流依赖性综合征是一种罕见但严重的并发症,导致颅内压和神经缺陷增加。可能的机制仍然存在争议。我们展示了我们对并发症的治疗的经验,并试图找到更好的并发症治疗策略。方法治疗中窝瓣囊肿囊肿的两个儿童接受CP分流,固定压力导管在7cmH_(2)o的开口压力下,然后开发依赖综合征。通过保留分流器,通过迷你侵入性囊肿壁切除有效治疗两种患者。回顾性地审查了临床表现,放射发现,治疗方法和治疗方法。结果分别从分流手术到分流综合征发生的时间分别为4和2年。脑的计算机断层摄影/磁共振调查结果显示出具有正常或小型心室的显着坍塌的囊肿。保留了两种患者进行二次迷你侵入性囊肿壁切除和分流导管。在运营之后,除了一个略微改善的视力障碍之外,它们的症状被解决。结论分流依赖综合征是CP分流的罕见但危险的并发症,应及时对待。塌陷和增厚的囊间间歇覆盖导管头端,由于慢性纤维化,脑依从性降低,以及脑脊液吸收的回归可能是发病机制。我们建议将残留囊间的锁孔切除作为有效和迷你侵袭性治疗选择。

著录项

  • 来源
    《Neuropediatrics》 |2018年第5期|共4页
  • 作者单位

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

    Department of Neurosurgery Tongji Hospital Tongji Medical College Huazhong University of Science;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经病学与精神病学;
  • 关键词

    shunt dependency syndrome; cyst-peritoneal shunt; arachnoid cyst; children;

    机译:分流依赖综合征;囊肿 - 腹膜分流;蛛网膜囊肿;儿童;

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