Vascular Center, Hôpital Marie Lannelongue, Groupe Hospitalier Paris Saint Joseph, Université Paris Saclay, Paris, France.
Stroke Unit, Hôpital Bicêtre, Le Kremlin-Bicêtre, Université Paris Sud, Paris, France.
J Vasc Surg. 2021 Apr;73(4):1290-1297. doi: 10.1016/j.jvs.2020.08.035. Epub 2020 Sep 1.
Atypical fibromuscular dysplasia (AFMD), also known as carotid web, is a rare underdiagnosed shelf-like fibrous tissue arising from the posterior carotid artery bulb that is a cause of cryptogenic stroke of the anterior cerebral vascularization. Despite the recurrence and severity of strokes caused by embolization associated with AFMD, there are no recommendations on the best strategy to manage single and bilateral lesions, which have unsatisfactory outcomes when treated with medical treatment exclusively.
From January 2016 to April 2019, 365 patients were operated on for a carotid stenosis in our institution. This cohort included 11 patients (3%), with a median age of 41 years (range, 39-51 years), referred by a stroke unit, treated for a symptomatic (10 strokes and 1 recurrent transient ischemic attack) AFMD lesion. Preoperative workup revealed a contralateral similar lesion in 45% of patients (5/11), which all also underwent surgery during a subsequent hospitalization. The diagnosis was confirmed by histologic examination when open surgery was performed. The 30-day and 1-year outcomes were retrospectively reviewed.
Of the 16 AFMD lesions operated, 13 were treated by open surgery (2 by classic endarterectomy and 11 by internal carotid resection-anastomosis) and 3 by carotid artery stenting, respectively, with a mean delay of 85.5 days and 20.5 days after the latest stroke. There was one complication after stenting (external iliac rupture) that was treated by a covered stent, and no perioperative complications after open surgery. The follow-ups at 30 days and 1 year were uneventful for all patients, without any deaths or stroke recurrences.
Symptomatic AFMD is a rare cause of cryptogenic stroke. Bilateral lesions are frequent. Early intervention is associated with favorable perioperative and 1-year outcomes. Open surgery is the first-line therapeutic option in this young patient population.
非典型性纤维肌发育不良(AFMD),也称为颈动脉网,是一种罕见的、诊断不足的后颈动脉球后出现的架子样纤维组织,是前脑血供部位不明原因中风的原因。尽管与 AFMD 相关的栓塞引起的中风复发和严重程度很高,但对于单一和双侧病变的最佳治疗策略尚无建议,单独采用药物治疗的效果不理想。
2016 年 1 月至 2019 年 4 月,我院对 365 例颈动脉狭窄患者进行了手术治疗。该队列包括 11 例(3%)患者,中位年龄 41 岁(范围 39-51 岁),因症状性(10 例中风和 1 例复发性短暂性脑缺血发作)AFMD 病变而被卒中病房转诊。术前检查发现 45%(5/11)的患者对侧有类似病变,所有患者在随后的住院期间均接受了手术治疗。当进行开放性手术时,通过组织学检查确认了诊断。回顾性分析了 30 天和 1 年的结果。
16 例 AFMD 病变中,13 例采用开放性手术治疗(2 例采用经典颈动脉内膜切除术,11 例采用颈内动脉切除吻合术),3 例采用颈动脉支架置入术治疗,平均延迟 85.5 天和 20.5 天后进行了最近的中风。支架置入后发生 1 例并发症(髂外动脉破裂),采用带膜支架治疗,开放性手术后无围手术期并发症。所有患者在 30 天和 1 年的随访中均无不良事件发生,无死亡或中风复发。
症状性 AFMD 是不明原因中风的罕见原因。双侧病变很常见。早期干预与良好的围手术期和 1 年结果相关。开放性手术是该年轻患者群体的一线治疗选择。