Institute of Diagnostic Radiology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Radiology, Riga Stradins University, Riga, Latvia.
Am J Case Rep. 2024 Mar 20;25:e942833. doi: 10.12659/AJCR.942833.
BACKGROUND Carotid-cavernous fistula (CCF) is a rare, atypical vascular shunt between the carotid arterial system and the venous channels of the cavernous sinus, classified according to the shunt's anatomy, by etiology (resulting from trauma or occurring spontaneously), or by hemodynamic characteristics (such as low- or high-flow fistulas). CASE REPORT A 62-year-old female patient with poorly controlled arterial hypertension presented with bilateral periorbital edema, conjunctival chemosis, ophthalmoplegia, diplopia, and diminished visual acuity. On magnetic resonance angiography (MRA), abnormal arterial flow along the cavernous sinuses was noted, suggestive of bilateral CCF. The diagnosis of indirect dural low-flow CCF (Barrow Type D) was later confirmed by digital subtraction angiography, with feeding arteries from intracavernous internal carotid artery branches, and meningeal branches of the external carotid artery, draining bilaterally to ophthalmic veins, the intracavernous sinus, and the inferior petrosal sinus. The patient was successfully treated with endovascular embolization. At 7-month follow-up, no residual arteriovenous shunting was detected. This case highlights the importance of non-invasive radiological methods for CCF, and presents rarely published radiological findings of bilateral Type-D dural CCFs on 3-dimensional time-of-flight MRA with post-treatment MRA follow-up. CONCLUSIONS Regardless of the patient's history of possible trauma, a patient presenting with bilateral periorbital edema, conjunctival chemosis, ophthalmoplegia, diplopia, and diminished visual acuity should have a spontaneous bilateral CCF investigated to prevent delayed treatment. Experienced neuroradiologists are needed to accurately detect indirect CCF, since this condition often does not demonstrate classic symptoms.
颈动脉海绵窦瘘(CCF)是一种罕见的、非典型的颈动脉系统与海绵窦静脉通道之间的血管分流,根据分流的解剖结构、病因(由创伤引起或自发性发生)或血流动力学特征(如低流量或高流量瘘)进行分类。
一名 62 岁女性患者,患有未控制的动脉高血压,表现为双侧眶周水肿、球结膜水肿、眼肌麻痹、复视和视力下降。磁共振血管造影(MRA)显示,海绵窦内异常动脉血流,提示双侧 CCF。数字减影血管造影(DSA)后诊断为间接硬脑膜低流量 CCF(Barrow 型 D),供血动脉来自海绵窦内颈动脉分支和颈外动脉脑膜分支,双侧引流至眼静脉、海绵窦和岩下窦。患者成功接受了血管内栓塞治疗。7 个月随访时,未发现残留动静脉分流。该病例强调了非侵入性放射学方法对 CCF 的重要性,并展示了罕见的双侧 D 型硬脑膜 CCF 的放射学表现,3D 时间飞跃 MRA 显示双侧 Type-D 硬脑膜 CCF,并进行了治疗后 MRA 随访。
无论患者是否有创伤史,出现双侧眶周水肿、球结膜水肿、眼肌麻痹、复视和视力下降的患者,都应调查是否存在自发性双侧 CCF,以避免延误治疗。需要有经验的神经放射学家来准确检测间接 CCF,因为这种情况通常没有典型的症状。