Carotid fibromuscular dysplasia and paresis of lower cranial nerves (Collect-Sicard syndrome). Case report.
Carotid fibromuscular dysplasia and paresis of lower cranial nerves (Collect-Sicard syndrome). Case report.
复制标题
颈动脉纤维肌性发育不良和下颅神经麻痹（Collect-Sicard 综合征）。
DOI：
10.3171/jns.1982.56.6.0850
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发表时间：
1982
影响因子：
4.1
通讯作者：
S. Cronqvist
中科院分区：
文献类型：
--
作者：
U. Havelius;B. Hindfelt;J. Brismar;S. Cronqvist
1例患者急性发作第9至第12脑神经单侧麻痹（Collet-Sicard综合征）。同侧逆行颈静脉造影和颈动脉血管造影显示颅底颈内动脉的不规则血管性变化，导致颈静脉孔下方的颈内静脉受压。这一发现的临床症状和体征进行了讨论，并检查可能的机制。家族史以及临床和X线检查结果与纤维肌性发育不良的诊断一致。
A patient suffered the acute onset of unilateral pareses of the ninth through 12th cranial nerves (Collet-Sicard syndrome). Ipsilateral retrograde jugular phlebography and carotid angiography revealed irregular aneurysmal changes of the internal carotid artery at the base of the skull, causing compression of the internal jugular vein below the jugular foramen. This finding is discussed in relation to the clinical symptoms and signs, and possible mechanisms are examined. Family history as well as the clinical and roentgenological findings were compatible with a diagnosis of fibromuscular dysplasia.