Vanikieti Kavin, Poonyathalang Anuchit, Jindahra Panitha, Cheecharoen Piyaphon, Chokthaweesak Wimonwan
Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
BMC Ophthalmol. 2018 Feb 2;18(1):25. doi: 10.1186/s12886-018-0687-4.
Cavernous carotid aneurysm (CCA) represents 2-9% of all intracranial aneurysms and 15% of internal carotid artery (ICA) aneurysms; additionally, giant aneurysms are those aneurysms that are > 25 mm in size. Bilateral CCAs account for 11-29% of patients and are commonly associated with structural weaknesses in the ICA wall, secondary to systemic hypertension. CCAs are considered benign lesions, given the low risk for developing major neurologic morbidities (i.e., subarachnoid hemorrhage, cerebral infarction, or carotid cavernous fistula). Moreover, concurrent presentation with posterior circulation cerebral infarction is even rarer, given different circulation territory from CCA. Here, we report on a patient with bilateral giant CCAs who presented with both typical and atypical symptoms.
An 88-year-old hypertensive woman presented with acute vertical oblique binocular diplopia, followed by complete ptosis of the right eye. Ophthalmic examination showed dysfunction of the right third, fourth, and sixth cranial nerves. Further examination revealed hypesthesia of the areas supplied by the ophthalmic (V1) and maxillary (V2) branches of the right trigeminal nerve. Bilateral giant cavernous carotid aneurysms, with a concurrent subacute right occipital lobe infarction, were discovered on brain imaging and angiogram. Additionally, a prominent right posterior communicating artery (PCOM) was revealed. Seven months later, clinical improvement with stable radiographic findings was documented without any intervention.
Dysfunction of the third, fourth, and sixth cranial nerves, and the ophthalmic (V) and maxillary (V) branches of the trigeminal nerves, should necessitate brain imaging, with special attention given to the cavernous sinus. Despite unilateral symptomatic presentation, bilateral lesions cannot be excluded solely on the basis of clinical findings. CCA should be included in the differential diagnosis of cavernous sinus lesions. Although rare, ipsilateral posterior circulation cerebral infarction (i.e., occipital lobe infarction) can occur in CCA patients, presumably as a result of distal embolization through an ipsilateral, prominent PCOM. Spontaneous clinical improvement with stable radiographic support may occur.
海绵窦段颈内动脉瘤(CCA)占所有颅内动脉瘤的2% - 9%,占颈内动脉(ICA)动脉瘤的15%;此外,巨大动脉瘤是指直径大于25mm的动脉瘤。双侧CCA占患者的11% - 29%,通常与ICA壁的结构薄弱有关,继发于系统性高血压。鉴于发生主要神经病变(即蛛网膜下腔出血、脑梗死或颈动脉海绵窦瘘)的风险较低,CCA被认为是良性病变。此外,由于与CCA的循环区域不同,同时出现后循环脑梗死的情况更为罕见。在此,我们报告一例双侧巨大CCA患者,其出现了典型和非典型症状。
一名88岁的高血压女性,最初表现为急性垂直性斜向双眼复视,随后右眼完全上睑下垂。眼科检查显示右侧第三、第四和第六脑神经功能障碍。进一步检查发现右侧三叉神经眼支(V1)和上颌支(V2)所支配区域感觉减退。脑部影像学检查和血管造影发现双侧巨大海绵窦段颈内动脉瘤,同时伴有亚急性右侧枕叶梗死。此外,还发现右侧后交通动脉(PCOM)明显增粗。七个月后,未经任何干预,临床症状改善,影像学检查结果稳定。
第三、第四和第六脑神经以及三叉神经眼支(V)和上颌支(V)功能障碍时,应进行脑部影像学检查,尤其要关注海绵窦。尽管临床表现为单侧症状,但不能仅凭临床发现排除双侧病变。CCA应列入海绵窦病变的鉴别诊断。虽然罕见,但CCA患者可能会发生同侧后循环脑梗死(即枕叶梗死),推测是由于通过同侧增粗的PCOM发生远端栓塞所致。可能会出现影像学检查结果稳定的自发性临床改善。