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无硬脑膜动静脉瘘的静脉性高血压性脊髓病相关的脑干出血:病例说明

Brainstem hemorrhage associated with venous hypertensive myelopathy without dural arteriovenous fistula: illustrative case.

作者信息

Hanai Sho, Yanaka Kiyoyuki, Akimoto Ken, Marushima Aiki, Nakamura Kazuhiro, Takahashi Nobuyuki, Matsumaru Yuji, Ishikawa Eiichi

机构信息

Departments of Neurosurgery, Tsukuba Memorial Hospital, Tsukuba, Ibaraki, Japan.

Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.

出版信息

J Neurosurg Case Lessons. 2024 Nov 4;8(19). doi: 10.3171/CASE24441.

DOI:10.3171/CASE24441
PMID:39496151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11539286/
Abstract

BACKGROUND

Venous hypertensive myelopathy (VHM), formerly known as "Foix-Alajouanine syndrome," is a spinal cord dysfunction caused by impaired perfusion of the spinal cord. Most cases are attributed to spinal dural arteriovenous fistulas (dAVFs), but there are scattered reports of VHM without concomitant dAVF. Furthermore, no cases of VHM associated with intracranial hemorrhage exist.

OBSERVATIONS

A 68-year-old man with a history of hypertension presented with a sudden headache, proximal paresis of the left upper extremity, impaired pain and temperature sensation in the right upper extremity, dysphagia, and dysarthria. Computed tomography scans showed intraparenchymal hemorrhage in the left medulla oblongata and a linear, continuous high-density area extending from the medulla oblongata to the cervical spinal cord. Magnetic resonance images showed cervical spondylosis at the C5-6 and C6-7 levels, with high signal intensity changes from the medulla oblongata to the lower cervical cord on T2-weighted images. Cerebral angiography showed no abnormal vessels. Conservative treatment gradually improved symptoms and the high signal intensity areas.

LESSONS

This case highlights intracranial hemorrhage occurring from extracranial causes and the possibility of VHM due to cervical spondylosis. When hemorrhagic lesions of the craniovertebral junction or spinal parenchymal lesions are encountered, the underlying pathology should be investigated thoroughly and systematically. https://thejns.org/doi/10.3171/CASE24441.

摘要

背景

静脉性高血压脊髓病(VHM),以前称为“福-阿二氏综合征”,是一种由脊髓灌注受损引起的脊髓功能障碍。大多数病例归因于硬脊膜动静脉瘘(dAVF),但也有散在报道称VHM不伴有dAVF。此外,尚无VHM与颅内出血相关的病例。

观察结果

一名68岁有高血压病史的男性,出现突发头痛、左上肢近端无力、右上肢痛温觉减退、吞咽困难和构音障碍。计算机断层扫描显示左延髓实质内出血,以及从延髓延伸至颈髓的线性连续高密度区。磁共振成像显示C5-6和C6-7水平的颈椎病,T2加权图像上从延髓到下颈髓有高信号强度改变。脑血管造影未显示异常血管。保守治疗使症状和高信号强度区逐渐改善。

经验教训

该病例突出了颅外原因导致的颅内出血以及颈椎病引起VHM的可能性。当遇到颅颈交界区出血性病变或脊髓实质病变时,应全面、系统地调查其潜在病理。https://thejns.org/doi/10.3171/CASE24441

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/a7e74d416895/CASE24441_figure_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/7b91eb47cfe3/CASE24441_figure_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/1ce2cfecf0ac/CASE24441_figure_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/0b95c878b2dc/CASE24441_figure_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/a7e74d416895/CASE24441_figure_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/7b91eb47cfe3/CASE24441_figure_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/1ce2cfecf0ac/CASE24441_figure_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/0b95c878b2dc/CASE24441_figure_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/11539286/a7e74d416895/CASE24441_figure_4.jpg

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本文引用的文献

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2
Perimedullary arteriovenous fistulas of the craniovertebral junction: A systematic review.颅颈交界区髓周动静脉瘘:一项系统评价
J Craniovertebr Junction Spine. 2020 Jul-Sep;11(3):157-162. doi: 10.4103/jcvjs.JCVJS_106_20. Epub 2020 Aug 14.
3
Revisiting the Vertebral Venous Plexus-A Comprehensive Review of the Literature.
重新审视椎静脉丛——文献综述
World Neurosurg. 2021 Jan;145:381-395. doi: 10.1016/j.wneu.2020.10.004. Epub 2020 Oct 10.
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Predictors of Outcome in Patients with Medullary Hemorrhage.影响延髓出血患者预后的因素分析。
J Stroke Cerebrovasc Dis. 2020 Dec;29(12):105337. doi: 10.1016/j.jstrokecerebrovasdis.2020.105337. Epub 2020 Sep 30.
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Management of brainstem haemorrhages.脑干出血的处理。
Swiss Med Wkly. 2019 Apr 5;149:w20062. doi: 10.4414/smw.2019.20062. eCollection 2019 Mar 25.
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