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Parkinsonism after Shunting for Hydrocephalus Secondary to Aqueductal Stenosis with Chiari Malformation

机译:伴有Chiari畸形的水管狭窄继发脑积水分流后的帕金森病

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Parkinsonism has been well-documented in patients with communicating hydrocephalus, but it is an uncommon complication of shunting for obstructive hydrocephalus secondary to aqueductal stenosis. Although a number of hypotheses regarding anatomical and pathophysiological clues to this are proposed, its exact mechanism remains unclear. The author presents a unique case of parkinsonism after shunting for hydrocephalus due to aqueductal stenosis with Chiari malformation. Suboccipital craniectomy and duraplasty followed by ventriculoperitoneal shunting was performed, parkinsonian symptoms developed after the shunt revision, and short-term levodopa therapy resulted in complete recovery. Case Report This 25-year-old man had a history of progressive headache during eight years before admission. He was admitted with increment in his headaches, drowsiness and vomiting with visual troubles; in the emergency room he was entubated because of development of loss of consciousness and bradycardia. Computerized tomography (CT) demonstrated obstructive hydrocephalus with a marked enlargement of lateral and 3rd ventricles (Figure 1). An external ventricular drainage (EVD) catheter was inserted to decrease the intracranial pressure. Magnetic resonance imaging (MRI) showed hydrocephalus associated with aqueductal stenosis, in addition to a hydromyelia extending from C2 to C5 level and tonsillar herniation confirming diagnosis of Chiari malformation type 1 (CM-1) (Figure 2). Following the removal of the EVD catheter, a suboccipital craniectomy and C1 laminectomy was performed. Intraoperative ultrasonography (US) revealed “pistoning” movement of the tonsils during systole-diastole pulsations. The dura mater was incised, the herniated tonsils were separated, and coagulated with achieving a free cerebrospinal fluid. Following duraplasty, valsalva maneuver was performed to ensure that foramen magnum obstruction by further tonsillar descent did not occur.
机译:帕金森氏症在有沟通性脑积水的患者中已有充分的文献记载,但因导水管狭窄继发梗阻性脑积水而进行分流并不常见。尽管提出了许多有关解剖学和病理生理学线索的假设,但其确切机制仍不清楚。作者介绍了因Chiari畸形导致导水管狭窄导致脑积水分流后发生帕金森病的独特案例。进行了枕下颅骨切除和硬膜成形术,然后进行脑室-腹膜分流,分流翻修后出现了帕金森氏症状,短期的左旋多巴治疗导致完全恢复。病例报告该25岁的男子在入院前八年内有进行性头痛的病史。他因头痛,嗜睡和视觉障碍呕吐而入院。在急诊室,他因失去意识和心动过缓而入院。计算机断层扫描(CT)显示梗阻性脑积水,侧脑室和第三脑室明显增大(图1)。插入外部心室引流(EVD)导管以​​降低颅内压。磁共振成像(MRI)显示脑积水与导水管狭窄相关,此外还有从C2延伸至C5的脑脊髓积液和扁桃体突出症,证实了1型Chiari畸形(CM-1)的诊断。移除EVD导管后,进行枕下颅骨切除和C1椎板切除。术中超声检查(US)显示在心脏舒张期搏动期间扁桃体“活塞运动”。切开硬脑膜,分离扁桃体突出的扁桃体,使其凝结形成游离的脑脊液。硬脊膜成形术后,进行valsalva手术以确保不会发生进一步扁桃体下降所致的大孔阻塞。

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