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[巨长基底动脉所致球血管压迫表现为神经源性难治性高血压]

[Bulbovascular compression by megadolichobasilar artery manifested as neurogenic and refractory hypertension].

作者信息

Ishikawa Tatsuya, Nagayama Masao, Iida Masahiro, Shinohara Yukito

机构信息

Department of Neurology, Tokai University School of Medicine.

出版信息

Rinsho Shinkeigaku. 2004 Jun;44(6):359-64.

Abstract

A 37-year-old man with juvenile and refractory hypertension was admitted to our hospital for progressive left hearing loss, vertigo, and dizziness. Neurological examination revealed left hearing loss and exaggerated deep tendon reflexes and vestibular dysfunction. MRI and cerebral angiography disclosed megadolichobasilar artery (MDBA). Moreover, modified MR cisternography at the medulla disclosed marked compression and deformity of the left rostral ventrolateral medulla (RVLM) by the dolichoectatic right vertebral artery. In the literatures, bulbovascular compression has been reported in 4 among 9 patients with MDBA (including the present patient), for whom MRI of the medulla was presented. All 4 patients suffered from hypertension, and at least 3 of them showed juvenile and refractory hypertension. Ipsilateral pyramidal tract disturbance (Opalski syndrome) was observed in 3 patients. Considering the recent concept that the cardiovascular center can be localized at the RVLM, juvenile and refractory hypertension, and possibly Opalski syndrome in the present patient can be attributed to bulbovascular compression by MDBA. In the patients with MDBA and hypertension or Opalski syndrome, MR cisternography of the medulla is warranted to evaluate compression by MDBA.

摘要

一名37岁患有青少年难治性高血压的男性因进行性左耳听力丧失、眩晕和头晕入住我院。神经系统检查发现左耳听力丧失、深腱反射亢进和前庭功能障碍。MRI和脑血管造影显示存在巨大延长基底动脉(MDBA)。此外,延髓改良磁共振脑池造影显示,扩张延长的右侧椎动脉对左侧延髓嘴侧腹外侧区(RVLM)造成明显压迫和变形。在文献中,9例MDBA患者(包括本例患者)中有4例进行了延髓MRI检查,报告存在延髓血管压迫。所有4例患者均患有高血压,其中至少3例为青少年难治性高血压。3例患者出现同侧锥体束障碍(奥帕尔斯基综合征)。鉴于最近认为心血管中枢可定位于RVLM的观点,本例患者的青少年难治性高血压以及可能的奥帕尔斯基综合征可归因于MDBA导致的延髓血管压迫。对于患有MDBA和高血压或奥帕尔斯基综合征的患者,有必要进行延髓磁共振脑池造影以评估MDBA造成的压迫。

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