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Loeys-Dietz 综合征患者的脑动脉瘤夹闭术:病例报告。

Clipping of a cerebral aneurysm in a patient with Loeys-Dietz syndrome: case report.

机构信息

Division of Neurosurgery, Duke University Medical Center, Durham, North Carolina 27710, USA

出版信息

Neurosurgery. 2011 Sep;69(3):E746-55; discussion E55. doi: 10.1227/NEU.0b013e31821964a3.

Abstract

BACKGROUND AND IMPORTANCE

his is the first case report of clipping a cerebral aneurysm in a patient with Loeys-Dietz syndrome (LDS). LDS is a newly described autosomal dominant connective tissue disease with systemic vascular involvement. Unique to this syndrome is the development of aneurysms at a young age with the propensity of dissection or rupture at a stage that is earlier than when surgical intervention is typically indicated. We describe the nuances in intraoperative and postoperative management.

CLINICAL PRESENTATION

A 31-year-old woman who recently received a diagnosis of with LDS type II presented to neurosurgical attention for management of an unruptured right ophthalmic artery aneurysm. The patient underwent a right pterional craniotomy for clipping of the aneurysm, with lumbar drain placement before the procedure. Papaverine had to be used several times to counteract vasospasm of the vessels during arachnoid dissection. Because of vascular reactivity, temporary clipping was not used, and the aneurysm was clipped successfully.

CONCLUSION

LDS is a newly described disorder that warrants awareness in the neurosurgical community because of its association with intracerebral aneurysms as well as craniosynostosis (19%), scoliosis (20%), cervical spine instability (7%), hydrocephalus, and Arnold-Chiari malformation. When clipping aneurysms in these patients, the surgeon should be aware of the potential for severe vascular reactivity during dissection and avoid temporary clipping when possible. Avoidance of lumbar drainage intraoperatively reduces the risk of intracranial hypotension after removal.

摘要

背景与重要性

这是首例 Loeys-Dietz 综合征(LDS)患者颅内动脉瘤夹闭的病例报告。LDS 是一种新描述的常染色体显性结缔组织疾病,伴有系统性血管受累。该综合征的独特之处在于,年轻患者就会发生动脉瘤,而且在通常需要手术干预的阶段之前,就有夹层或破裂的倾向。我们描述了术中及术后管理的细微差别。

临床表现

一名 31 岁女性最近被诊断为 LDS Ⅱ型,因未破裂的右侧眼动脉动脉瘤而接受神经外科治疗。患者行右侧翼点开颅术夹闭动脉瘤,术前放置腰椎引流管。在蛛网膜剥离过程中,血管痉挛多次使用罂粟碱来对抗。由于血管反应性,未使用临时夹闭,成功夹闭了动脉瘤。

结论

LDS 是一种新描述的疾病,由于其与颅内动脉瘤以及颅缝早闭(19%)、脊柱侧凸(20%)、颈椎不稳定(7%)、脑积水和 Arnold-Chiari 畸形有关,在神经外科领域应引起重视。在这些患者中夹闭动脉瘤时,外科医生应意识到在解剖过程中可能存在严重的血管反应,并尽可能避免临时夹闭。术中避免腰椎引流可降低术后颅内低血压的风险。

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