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血管型埃勒斯-当洛斯综合征患者的颈动脉夹层(Eagle 综合征所致):病例报告

Bilateral carotid artery dissection due to Eagle syndrome in a patient with vascular Ehlers-Danlos syndrome: a case report.

机构信息

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, 6-1 Kishibe-shimmachi, Suita, Osaka, 564-8565, Japan.

Department of Neurology, National Cerebral and Cardiovascular Center, 6-1 Kishibe-shimmachi, Suita, Osaka, 564-8565, Japan.

出版信息

BMC Neurol. 2020 Jul 21;20(1):285. doi: 10.1186/s12883-020-01866-2.

Abstract

BACKGROUND

Patients with vascular Ehlers-Danlos syndrome (EDS) occasionally suffer from arterial dissection. Eagle syndrome, which is caused by an elongated styloid process and also causes arterial dissection, is difficult to diagnose and could sometimes be overlooked. Little is known of the coexistence of these two diseases, and treatment strategy is not established. Here, we present a case of bilateral internal carotid artery (ICA) dissection due to Eagle syndrome in a patient with vascular EDS.

CASE PRESENTATION

A 30-year-old man was admitted to our hospital because of sudden onset of mild sensory disturbance in his left limbs. He had a history of Ehlers-Danlos syndrome (EDS) and also had left cervical internal carotid artery (ICA) dissection 3 years before. Diffusion-weighted imaging showed acute cerebral infarcts in the right hemisphere. Cervical computed tomography angiography (CTA) revealed the right ICA narrowing at the cervical portion in addition to the previous left cervical ICA dissection. Cervical magnetic resonance imaging (MRI) revealed double-lumen and intramural hematoma at the narrowing portion of the right cervical ICA, which indicates arterial dissection. CT also revealed bilateral elongated styloid processes which are close to each side of cervical ICA. We diagnosed him as bilateral ICA dissection due to bilateral Eagle syndrome. Considering vascular complications due to vascular EDS, we performed closer follow-up with transoral carotid ultrasonography (TOCU). In 4 months, his right ICA dissection gradually improved without stroke recurrence or deterioration of dissection.

CONCLUSIONS

Since patients with vascular EDS easily develop arterial dissection, Eagle syndrome may be overlooked. Clinicians should consider Eagle syndrome in the case of vascular EDS with extracranial ICA dissection and close follow-up should be prioritized in cases of Eagle syndrome with vascular EDS.

摘要

背景

血管型埃勒斯-当洛斯综合征(EDS)患者偶尔会发生动脉夹层。由细长茎突引起的鹰钩综合征也会导致动脉夹层,但这种疾病很难诊断,有时可能会被忽视。这两种疾病同时存在的情况知之甚少,治疗策略也尚未建立。本文报告了一例血管型 EDS 患者因鹰钩综合征而导致双侧颈内动脉(ICA)夹层的病例。

病例介绍

一名 30 岁男性因左侧肢体突发轻度感觉障碍而入院。他有 EDS 病史,3 年前曾发生左侧颈内动脉夹层。弥散加权成像显示右侧大脑半球急性脑梗死。颈椎 CT 血管造影(CTA)显示右侧颈内动脉在颈部狭窄,此外还存在先前的左侧颈内动脉夹层。颈椎磁共振成像(MRI)显示右侧颈内动脉狭窄部位存在双腔和壁内血肿,提示动脉夹层。CT 还显示双侧细长的茎突,靠近颈内动脉两侧。我们诊断为双侧鹰钩综合征导致双侧颈内动脉夹层。考虑到血管 EDS 引起的血管并发症,我们通过经口颈动脉超声(TOCU)进行了更密切的随访。4 个月后,他的右侧颈内动脉夹层逐渐改善,没有再次发生中风或夹层恶化。

结论

由于血管型 EDS 患者容易发生动脉夹层,鹰钩综合征可能会被忽视。对于有颅外 ICA 夹层的血管型 EDS 患者,临床医生应考虑鹰钩综合征;对于有血管型 EDS 的鹰钩综合征患者,应优先进行密切随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e768/7372806/d72e2f30aec3/12883_2020_1866_Fig1_HTML.jpg

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