Panameño Oscar A, Morales Jesus
Neurological Surgery, Hospital Jose Eleuterio Gonzalez, Universidad de Nuevo Leon, Monterrey, MEX.
Cureus. 2024 Nov 16;16(11):e73803. doi: 10.7759/cureus.73803. eCollection 2024 Nov.
The treatment of indirect carotid-cavernous fistula (CCF) poses a unique challenge. Currently, endovascular interventions remain the principal treatment option with high cure rates and acceptable safety profiles. The anatomical characteristics of individual cases determine the optimal vascular access routes (transvenous vs. transarterial), and the devices utilized to achieve therapeutic goals. We present a rare case of an indirect CCF in a 13-year-old patient with an anatomical variant of the ophthalmic artery and hemophilia. CCFs are infrequent in the pediatric population, and an association with a deep recurrent ophthalmic artery (DROA) and hemophilia presents a unique treatment challenge. The patient had been diagnosed with type A hemophilia in 2013. In November 2022, he had presented with insidious conjunctival hyperemia and developed gradual ocular proptosis. He had been referred to Ophthalmology in October 2023, with mild symptoms and no ocular bruit or visual acuity deterioration. Angio CT, angio MRI, and cerebral angiography at that time had shown an indirect CCF. The association of an anatomical variant with the indirect CCF led to adverse anatomy and failed transvenous/transarterial vascular access. Classic treatment options (coils, detachable balloons, and liquid embolic agents) are not feasible when selective microcatheterism is unsuccessful. A FRED flow diverter was placed in the cavernous segment of the internal carotid artery (ICA) as an off-label solution to adverse patient vascular anatomy. Successful device implantation resulted in the gradual resolution of the patient's ocular symptoms.
间接性颈内动脉海绵窦瘘(CCF)的治疗具有独特的挑战性。目前,血管内介入治疗仍然是主要的治疗选择,治愈率高且安全性可接受。个别病例的解剖特征决定了最佳的血管通路(经静脉与经动脉)以及用于实现治疗目标的器械。我们报告了一例罕见的13岁间接性CCF患者,其眼动脉存在解剖变异且患有血友病。CCF在儿科人群中并不常见,而与深部眼动脉复发(DROA)和血友病相关则带来了独特的治疗挑战。该患者于2013年被诊断为A型血友病。2022年11月,他出现隐匿性结膜充血,并逐渐发展为眼球突出。2023年10月,他因症状较轻且无眼部杂音或视力下降被转诊至眼科。当时的血管CT、血管MRI和脑血管造影显示为间接性CCF。解剖变异与间接性CCF的关联导致解剖结构不利,经静脉/经动脉血管通路失败。当选择性微导管插入术不成功时,经典的治疗选择(弹簧圈、可脱性球囊和液体栓塞剂)不可行。作为针对患者不利血管解剖结构的一种超说明书解决方案,在颈内动脉(ICA)海绵窦段置入了一个FRED血流导向装置。成功植入该器械后,患者的眼部症状逐渐缓解。