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巨大颈内动脉分叉处动脉瘤作为颅咽管瘤一种罕见且危险的鉴别诊断

A Giant Internal Carotid Bifurcation Aneurysm as a Rare and Dangerous Differential Diagnosis of a Craniopharyngioma.

作者信息

Perret Caio M, Bertani Raphael, W Koester Stefan, Santa Maria Paulo Eduardo, Von Zuben Daniela, Batista Sávio, Schiavini Hugo C, Landeiro José Alberto

机构信息

Neurological Surgery, Hospital Municipal Miguel Couto, Rio de Janeiro, BRA.

Neuroscience, Federal University of Rio de Janeiro, Rio de Janeiro, BRA.

出版信息

Cureus. 2022 Jan 25;14(1):e21588. doi: 10.7759/cureus.21588. eCollection 2022 Jan.

DOI:10.7759/cureus.21588
PMID:35228946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8867713/
Abstract

Craniopharyngiomas are supra/parasellar lesions that often present with general, unspecific symptoms. Similarly, internal carotid artery (ICA) bifurcation giant aneurysms may also produce calcified, heterogeneous, parasellar expansive lesions, posing a relevant differential diagnosis due to their inherently different surgical strategies and risks. We report the case of a 54-year-old female presenting with progressive disorientation and apathetic behavior. CT and MRI reports described a suprasellar heterogenous mass with calcifications associated with an adjacent, laterally located fluid collection suggestive of a craniopharyngioma. During the surgical procedure, perfuse and unexplained arterial bleeding ensued, prompting the surgical team to review a previous contrast-enhanced CT scan. Careful inspection revealed an image suggestive of vascular pathology, with an area of continuous hyperdensity along the right ICA bifurcation. The Sylvian fissure was dissected, and an aneurysmal neck was encountered and successfully clipped. Giant intracranial aneurysms are rare but essential differential diagnoses to be considered during the workup and surgical approach toward parasellar mass lesions. This case illustrates the importance of performing a CT angiogram (CTA) for skull base lesions, even when the size is more suggestive of tumor pathology.

摘要

颅咽管瘤是鞍上/鞍旁病变,常表现为一般的非特异性症状。同样,颈内动脉(ICA)分叉处巨大动脉瘤也可能产生钙化、异质性、鞍旁膨胀性病变,由于其固有的不同手术策略和风险,构成了相关的鉴别诊断。我们报告一例54岁女性,表现为进行性定向障碍和淡漠行为。CT和MRI报告描述了一个鞍上异质性肿块,伴有钙化,与相邻的外侧液体积聚有关,提示颅咽管瘤。在手术过程中,出现了大量且无法解释的动脉出血,促使手术团队复查之前的增强CT扫描。仔细检查发现一个提示血管病变的图像,沿右侧ICA分叉处有一个连续的高密度区域。解剖外侧裂,遇到动脉瘤颈并成功夹闭。巨大颅内动脉瘤很少见,但在对鞍旁肿块病变进行检查和手术时,是必须考虑的重要鉴别诊断。该病例说明了即使病变大小更提示肿瘤病理,对颅底病变进行CT血管造影(CTA)的重要性。