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婴儿的副视神经管和颈动脉床突孔:小儿人群前床突切除术的考量因素

Accessory optic canals and a caroticoclinoid foramen in an infant: considerations for anterior clinoidectomy in the pediatric population.

作者信息

Cowher Abigail E, Zdilla Matthew J

机构信息

Department of Pathology, Anatomy, and Laboratory Medicine (PALM), West Virginia University School of Medicine, Morgantown, West Virginia, USA.

出版信息

Arch Pediatr Neurosurg. 2024 May;6(2). doi: 10.46900/apn.v6i1.233. Epub 2024 Mar 5.

DOI:10.46900/apn.v6i1.233
PMID:41018044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12466191/
Abstract

INTRODUCTION/BACKGROUND: Anterior clinoidectomy is a routine neurosurgical procedure for the management of paraclinoid aneurysms and tumors in adults; however, it has been performed less extensively in children. The anterior clinoid process of the sphenoid bone is closely related to vital neurovascular structures including the optic nerve, internal carotid artery, and the ophthalmic artery. Therefore, sphenoidal variants, such as the accessory optic canal and caroticoclinoid foramen, pose serious complications in anterior clinoidectomy including potential blindness and death.

CASE PRESENTATION

This report presents a novel case of concomitant bilateral accessory optic canals and a right-sided caroticoclinoid foramen found within an infantile sphenoid of a 12-month-old black male. The case report documents two co-occurring, clinically relevant variants known to complicate anterior clinoidectomy in an individual from a population that has been underrepresented in the literature.

CONCLUSIONS

Caroticoclinoid foramina and accessory optic canals can be mistaken for each other on preoperative imaging, and accessory optic canals can additionally be mistaken for pneumatization of the anterior clinoid process, lesser sphenoidal wing, or optic strut. A high index of suspicion for these anatomic variants on preoperative imaging could enable the prevention of adverse outcomes, including hemorrhaging of the internal carotid artery and/or ophthalmic artery and subsequent blindness or death.

摘要

引言/背景:前床突切除术是治疗成人鞍旁动脉瘤和肿瘤的常规神经外科手术;然而,在儿童中开展得较少。蝶骨的前床突与包括视神经、颈内动脉和眼动脉在内的重要神经血管结构密切相关。因此,蝶骨变异,如副视神经管和颈动脉床突孔,在前床突切除术中会引发严重并发症,包括潜在的失明和死亡。

病例介绍

本报告介绍了一例12个月大黑人男婴蝶骨中同时存在双侧副视神经管和右侧颈动脉床突孔的罕见病例。该病例报告记录了两种同时出现的、临床相关的变异,在文献中报道较少的人群个体中,这些变异会使前床突切除术变得复杂。

结论

颈动脉床突孔和副视神经管在术前影像学检查中可能相互误诊,副视神经管还可能被误诊为前床突、蝶骨小翼或视神经柱的气化。术前影像学检查对这些解剖变异保持高度怀疑指数,可预防不良后果,包括颈内动脉和/或眼动脉出血以及随后的失明或死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7a/12466191/63c63e27115f/nihms-2111883-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7a/12466191/be865484a2a7/nihms-2111883-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7a/12466191/63c63e27115f/nihms-2111883-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7a/12466191/be865484a2a7/nihms-2111883-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7a/12466191/63c63e27115f/nihms-2111883-f0002.jpg

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