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颈内动脉冗长迂曲患儿的临床变异性

Clinical variability in children with dolichoarteriopathies of the internal carotid artery.

作者信息

Foiadelli Thomas, Ippolito Rosario, Corbetta Riccardo, Simoncelli Anna Maria, Amariti Rossella, Licari Amelia, Marseglia Gianluigi, Savasta Salvatore

机构信息

Pediatric Clinic, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.

Vascular Surgery Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

出版信息

Childs Nerv Syst. 2020 Mar;36(3):621-628. doi: 10.1007/s00381-019-04395-7. Epub 2019 Nov 7.

Abstract

INTRODUCTION

Dolichoarteriopathies of the internal carotid artery (DICA) are frequent non-atheromatous anatomical changes in the general population. The etiology of DICA is still controversial: several hypotheses have been suggested, including an anomaly of embryological development, or a degenerative loss of elasticity of the vessel wall. DICA have been related to a wide spectrum of clinical presentations in adults, varying from asymptomatic forms to acute cerebrovascular events. However, to date, only a few pediatric cases have been reported.

METHODS AND RESULTS

We report seven patients with DICA, 6 males and 1 female, aged 3 to 13 years, presenting with variable clinical symptoms. Different imaging techniques, including color Doppler ultrasound and magnetic resonance angiography, were used to show loops and/or kinking of the ICA. Three of these patients received a diagnosis of Ehlers-Danlos syndrome (EDS).

DISCUSSION

This study highlights the clinical variability in pediatric patients with DICA. We emphasize the need for close clinical management of pediatric DICA. Finally, considering the long-term prognostic implications of EDS, we recommend specific testing in children with DICA and suspicious clinical signs of this pathology.

摘要

引言

颈内动脉冗长迂曲(DICA)是普通人群中常见的非动脉粥样硬化性解剖学改变。DICA的病因仍存在争议:已提出多种假说,包括胚胎发育异常或血管壁弹性的退行性丧失。DICA与成人广泛的临床表现相关,从无症状形式到急性脑血管事件不等。然而,迄今为止,仅报道了少数儿科病例。

方法与结果

我们报告了7例DICA患者,6例男性和1例女性,年龄3至13岁,表现出不同的临床症状。使用包括彩色多普勒超声和磁共振血管造影在内的不同成像技术显示颈内动脉的襻和/或扭结。其中3例患者被诊断为埃勒斯-当洛综合征(EDS)。

讨论

本研究强调了儿科DICA患者的临床变异性。我们强调对儿科DICA进行密切临床管理的必要性。最后,考虑到EDS的长期预后影响,我们建议对患有DICA且有该病理可疑临床体征的儿童进行特定检测。

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