Mansour Moustafa A, Refaat Ahmed, Kamer-Eldawla Ahmed M, Zohney Michael, El-Batanony Mohamed, Selim Mohammad M, Elshaer Ahmed M, Mostafa Hamdi Nabawi
Neurosurgery Department, Nasser Institute for Research and Treatment, Cairo, Egypt.
Department of Neurosurgery, Faculty of Medicine, Misr University for Science and Technology, Giza, Egypt.
J Neurosurg Case Lessons. 2025 Jul 28;10(4). doi: 10.3171/CASE25257.
Idiopathic normal pressure hydrocephalus (iNPH) typically manifests with the classic Hakim-Adams triad of gait disturbance, cognitive impairment, and urinary incontinence. While akinetic mutism represents a rare and severe neurological presentation characterized by profound reduction in voluntary movement and speech, its association with iNPH remains underrecognized in clinical practice. This case illustrates both the diagnostic challenges and remarkable therapeutic potential when encountering this unusual manifestation of iNPH.
A previously healthy 52-year-old female developed progressive gait instability, urinary incontinence, and cognitive decline over 6 months, followed by 3 months of akinetic mutism. Examination demonstrated characteristic features of iNPH including paratonic rigidity, magnetic gait, and frontal release signs. Neuroimaging revealed moderate ventriculomegaly with an Evans index of 0.38 and hyperdynamic CSF flow dynamics (peak velocity 7.4 cm/sec, stroke volume 95 µL). The patient exhibited dramatic clinical improvement within 1 week of ventriculoperitoneal shunt placement, with complete resolution of akinetic mutism and significant recovery of other symptoms sustained at the 6-month follow-up.
This case underscores that akinetic mutism, while uncommon, may represent a severe but treatable manifestation of iNPH. The rapid reversal of akinetic mutism following CSF diversion highlights the importance of considering iNPH even in atypical presentations. Quantitative CSF flow analysis emerges as a valuable diagnostic tool in such challenging cases, while the striking clinical response reinforces the potential for complete functional recovery with timely intervention. https://thejns.org/doi/10.3171/CASE25257.
特发性正常压力脑积水(iNPH)通常表现为经典的哈基姆 - 亚当斯三联征,即步态障碍、认知障碍和尿失禁。运动不能性缄默症是一种罕见且严重的神经学表现,其特征为自主运动和言语显著减少,然而在临床实践中,它与iNPH的关联仍未得到充分认识。本病例展示了在遇到iNPH这种不寻常表现时的诊断挑战和显著的治疗潜力。
一名既往健康的52岁女性在6个月内出现进行性步态不稳、尿失禁和认知功能下降,随后出现3个月的运动不能性缄默症。检查显示iNPH的特征性表现,包括 gegenhalten 强直、磁性步态和额叶释放征。神经影像学检查显示中度脑室扩大,埃文斯指数为0.38,脑脊液流动动力学活跃(峰值速度7.4 cm/秒,每搏量95 μL)。患者在脑室腹腔分流术后1周内临床症状显著改善,运动不能性缄默症完全消失,其他症状在6个月随访时也有明显恢复。
本病例强调,运动不能性缄默症虽不常见,但可能是iNPH的一种严重但可治疗的表现。脑脊液引流后运动不能性缄默症迅速逆转,凸显了即使在非典型表现中也需考虑iNPH的重要性。在这种具有挑战性的病例中,定量脑脊液流动分析成为一种有价值的诊断工具,而显著的临床反应则强化了及时干预实现完全功能恢复的潜力。https://thejns.org/doi/10.3171/CASE25257 。
需注意,文中“gegenhalten 强直”为医学术语,可能存在更准确的中文表述,具体可根据医学专业规范进一步调整。