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Deep Brain Stimulation Surgery for Parkinson Disease Coexisting With Communicating Hydrocephalus: A Case Report

机译:深部脑刺激手术治疗帕金森病并发脑积水并存:一例报告

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摘要

We report a successful bilateral globus pallidus internus-deep brain stimulation (GPi-DBS) for a Parkinson disease (PD) patient with idiopathic normal pressure hydrocephalus (INPH) and an unusually long anterior commissure-posterior commissure (AC-PC) line. A 54-year-old man presented with a history of 3 months of severe shuffling gait, rigidity, slow movements of the left side limbs, and difficulty managing finances. A brain MRI revealed marked ventriculomegaly (Evans index = 0.42). The patient was diagnosed with INPH and a ventriculoperitoneal shunt was placed. Cognitive impairment improved, but walking disturbances, slowness, and rigidity persisted. Then treatment with levodopa was added, and the patient experienced a sustained improvement. He was diagnosed with PD. After 7 years, the patient developed gait freezing and severe levodopa-induced dyskinesia. The patient underwent bilateral GPi-DBS. We used MRI/CT fusion techniques for anatomical indirect targeting. Indirect targeting is based on standardized stereotactic atlas and on a formula—derived method based on AC-PC landmarks. The AC-PC line was 40 mm (the usual length is between 19 and 32 mm). Intraoperative microelectrode recording was a non-expendable test, but multiple recordings were avoided to reduce the surgical risk of ventricular involvement. There was a 71% decrease in the UPDRS III score during the on-stimulation state (28 to 8). The patient's dyskinesias resolved dramatically with a UdysRS of 15 (88% improvement) during the on-stimulation condition. The observed motor benefits and the improvement of his daily activities have persisted 6 months after surgery. Deep brain stimulation surgery in PD with ventriculomegaly is a challenge. This procedure can result in a greater chance of breaching the ventricle, with risks of intraventricular hemorrhage and migration of cerebrospinal fluid into the brain parenchyma with target displacement. Furthermore, clinical judgment is paramount when recent onset of shuffling gait coexists with ventriculomegaly because the most common dilemma is differentiating between PD and INPH. For these reasons, neurologists and surgeons may refuse to operate on PD patients with ventriculomegaly. However, DBS should be considered for PD patients with motor complications when responsiveness to levodopa is demonstrated, even in the context of marked ventriculomegaly.
机译:我们报告成功的帕金森病(PD)患者患有特发性正常压积性脑积水(INPH)和异常长的前连合-后连合(AC-PC)线的双侧苍白球内侧-深部脑刺激(GPi-DBS)。一名54岁的男子有3个月的严重步态步态,僵硬,左侧肢体动作缓慢以及财务管理困难的病史。脑部MRI显示明显的心室肥大(Evans指数= 0.42)。该患者被诊断出患有INPH,并进行了心室腹膜分流。认知障碍得到改善,但步行障碍,缓慢和僵硬仍然存在。然后加入左旋多巴治疗,患者持续改善。他被诊断出患有PD。 7年后,患者出现步态冻结和严重的左旋多巴诱发的运动障碍。该患者接受了双侧GPi-DBS。我们使用MRI / CT融合技术进行解剖学间接靶向。间接定位基于标准化的立体定位图集和基于AC-PC地标的公式得出的方法。 AC-PC线为40毫米(通常长度在19到32毫米之间)。术中微电极记录是一项不可消耗的测试,但避免了多次记录以减少外科手术对心室受累的风险。在刺激状态下(28到8),UPDRS III得分降低了71%。在刺激条件下,患者的运动障碍明显缓解,UdysRS为15(改善88%)。观察到的运动益处和他日常活动的改善在手术后6个月一直持续。 PD脑室肥大的深部脑刺激手术是一个挑战。此过程可能导致更大的脑室破裂机会,并伴有脑室出血和脑脊液迁移到目标位置的脑实质中的风险。此外,当最近的改组步态发作与心室肥大并存时,临床判断是最重要的,因为最常见的难题是区分PD和INPH。由于这些原因,神经科医生和外科医生可能会拒绝对PD合并心室肥大的患者进行手术。然而,当表现出对左旋多巴的反应性时,即使在明显的心室肥大的情况下,对于患有运动并发症的PD患者,也应考虑使用DBS。

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