用单侧半颅切除术和钛合金颅骨成形术治疗一名患有卡穆拉蒂-恩格尔曼病的儿童患者的高颅内压:示例病例。

Roboan Guillen Arguello, Nicholas Sader, J Gordon McComb
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引用次数: 0

摘要

背景:卡姆拉蒂-恩格尔曼病(Camurati-Engelmann disease,CED)是一种极其罕见的常染色体显性遗传疾病,可继发于颅骨骨质增生,导致颅内容积减少,从而引起颅内压(ICP)升高。在药物难治性病例中,降低 ICP 的手术方法包括颅内容量扩容和脑室腹腔分流术:作者介绍了一例患有 CED 和药物难治性 ICP 增高的儿童患者,该患者接受了单侧半颅骨切除术和钛颅骨成形术,结果症状长期完全缓解:https://thejns.org/doi/10.3171/CASE24590。
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Unilateral hemicraniectomy with titanium cranioplasty for the treatment of high intracranial pressure in a pediatric patient with Camurati-Engelmann disease: illustrative case.

Background: Camurati-Engelmann disease (CED) is an extremely rare autosomal dominant genetic disorder that can cause increased intracranial pressure (ICP) secondary to cranial hyperostosis, which decreases intracranial volume. Surgical procedures to reduce ICP in medically refractory cases include intracranial volume expansion and ventriculoperitoneal shunting.

Observations: The authors present the case of a pediatric patient with CED and medically refractory increased ICP who underwent unilateral hemicraniectomy with titanium cranioplasty, resulting in a complete long-term resolution of symptoms.

Lessons: Unilateral hemicraniectomy with titanium cranioplasty is a feasible surgical treatment for CED in pediatric patients with medically refractory increased ICP and papilledema. https://thejns.org/doi/10.3171/CASE24590.

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