高须动脉炎的冠状椎侧支1例

Andey V. Chupin, A. Zotikov, A. S. Kutovaya, A. L. Golovyuk, Aleksandr F. Kharazov, V. A. Kul’bak, A. Kozhanova, A. Varava, Irina E. Tiimina
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引用次数: 0

摘要

简介:非特异性大动脉炎是一种罕见的自身免疫性疾病,主要表现为主动脉及其分支受累和变窄,导致相应动脉区域缺血。在俄罗斯联邦境内,Takayasu非特异性大动脉炎最常见的表现是主动脉弓分支的病变,在极少数情况下导致所谓的秃弓综合征的发展。在缺氧的情况下,通过新生血管生成或血流从闭塞血管转向小直径血管形成系统间侧枝。在秃顶弓综合征患者中,椎动脉在脑供血中起着关键作用。在这里,侧枝血供是通过系统间吻合实现的,最常见的是通过肋间动脉和胸内动脉之间的吻合口。在文献中,有冠状动脉和支气管动脉之间形成侧支的单一病例报道。本文报道一例重症高松动脉炎伴头臂干、右颈总动脉、左颈总动脉、右内颈总动脉、左内颈总动脉(秃弓综合征)闭塞的临床病例。这种病程的可能原因是病人转诊较晚和缺乏适当的基本治疗。结论:本病例是世界文献中第4例冠状动脉与脑动脉之间存在络的病例,也是世界文献中第1例左右冠状动脉至椎动脉之间存在络的病例。这种不寻常的侧支血供途径可以解释为锁骨下和肋间动脉系统缺乏侧支代偿的可能性,严重的慢性脑缺血。通常,非特异性大动脉炎患者心绞痛的原因是动脉炎向冠状动脉扩散、主动脉瓣功能不全、左心室肥厚。在上述病例中,这些条件都不存在,心绞痛只能归因于不寻常的络的存在和短暂性窃血综合征的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coronary-Vertebral Collaterals in Takayasu Arteritis: Case Report
INTRODUCTION: PNonspecific aortoarteritis is a rare autoimmune disease with the involvement and narrowing of the aorta and its branches leading to ischemia of the respective arterial region. In the territory of the Russian Federation, the most common manifestation of Takayasu nonspecific aortoarteritis is lesion of the branches of the aortic arch, which in rare cases leads to development of the so called bald arch syndrome. In response to hypoxia, intersystemic collaterals are formed through the neoangiogenesis or redirection of the blood flow from the occluded vessels to small-diameter vessels. In patients with bald arch syndrome, the key role in blood supply to the brain is played by the vertebral arteries. Here, collateral blood supply is realized through the intersystemic anastomoses, most often through the anastomotic leaks between the intercostal and internal thoracic arteries. In the literature, single cases of formation of collaterals between coronary and bronchial arteries are reported. The article presents a clinical case of coronary-vertebral anastomoses in a patient with extremely severe course of Takayasu arteritis with occlusion of the brachiocephalic trunk, right common carotid artery (CA), left common CA, right internal CA, left internal CA (bald arch syndrome). The probable cause of such course of the disease was late referral for medical help by the patient and lack of adequate basic therapy. CONCLUSION: The demonstrated case is the fourth case in the world literature describing the existence of collaterals between the coronary arteries and cerebral arteries, and the first case in the world describing the existence of collaterals from the right and left coronary arteries to the vertebral artery. Such unusual pathway of collateral blood supply in the patient is explained by the absence of the possibility for collateral compensation from the systems of subclavian and intercostal arteries, severe chronic cerebral ischemia. Usually, the causes of angina pectoris in patients with nonspecific aortoarteritis are spread of arteritis to the coronary arteries, insufficiency of the aortic valve, hypertrophy of the left ventricle. In the described case, none of these conditions was present, and angina can only be attributed to the existence of unusual collaterals and the development of a transient steal syndrome.
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