Kim Shin Hye, Han Seung Hoon, Song Yoonjae, Park Chang Sik, Song Jae-Jin
Korea University Medical Center, Korea University College of Medicine, Department of Otorhinolaryngology-Head and Neck Surgery, Seoul, Republic of Korea; Seoul National University Bundang Hospital, Seoul National University College of Medicine, Department of Otorhinolaryngology-Head and Neck Surgery, Seongnam, Republic of Korea.
Seoul National University Bundang Hospital, Seoul National University College of Medicine, Department of Otorhinolaryngology-Head and Neck Surgery, Seongnam, Republic of Korea.
Braz J Otorhinolaryngol. 2017 Nov-Dec;83(6):683-690. doi: 10.1016/j.bjorl.2016.09.004. Epub 2016 Oct 17.
Auricular Arteriovenous Malformation of the external ear is a rarely encountered disease; in particular, arteriovenous malformation arising from the auricle, with spontaneous bleeding, has seldom been reported.
In the current study, we report an unusual case of late-onset auricular arteriovenous malformation originating from the posterior auricular artery that was confirmed by computed tomographic angiography. The case was successfully managed by pre-surgical intravascular embolization followed by total lesion excision. Prompted by this case, we also present a scoping review of the literature.
A case of a 60 year-old man with right auricular arteriovenous malformation treated in our tertiary care center, and 52 patients with auricular arteriovenous malformation described in 10 case reports and a retrospective review are presented. Auricular arteriovenous malformation can manifest as swelling of the ear, pulsatile tinnitus, pain, and/or bleeding. On physical examination, a pulsatile swelling and/or a tender mass is evident. When arteriovenous malformation is suspected, the lesions should be visualized using imaging modalities that optimally detect vascular lesions, and managed via embolization, mass excision, or auricular resection. Effectiveness of the various diagnostic methods used and the treatment outcomes were analyzed.
Various imaging modalities including Doppler sonography, computed tomographic angiography, magnetic resonance angiography, and/or transfemoral cerebral angiography were used to diagnose 38 cases reported in the literature. In another 15 cases, no imaging was performed; treatment was determined solely by physical examination and auscultation. Of the total of 53 cases, 12 were not treated (their symptoms were merely observed) whereas 20 underwent therapeutic embolization. In total, 32 patients, including 1 patient who was not treated and 10 with persistent or aggravated arteriovenous malformation after previous embolization, underwent mass excision or auricular resection depending on the extent of the lesion. No major postoperative complication was recorded. The postoperative follow-up duration varied from 1 month to 19 years, and only one case of unresectable, residual cervicofacial arteriovenous malformation was recorded.
Auricular arteriovenous malformation is a rarely encountered disease, but should be suspected if a patient presents with a swollen ear and pulsatile tinnitus. Appropriate imaging is essential for diagnosis and evaluation of the extent of disease. As embolization affords only relatively poor control, total surgical removal of the vascular mass is recommended.
外耳耳动静脉畸形是一种罕见疾病;尤其是起源于耳廓且伴有自发性出血的动静脉畸形,鲜有报道。
在本研究中,我们报告一例罕见的迟发性耳动静脉畸形病例,起源于耳后动脉,经计算机断层血管造影证实。该病例通过术前血管内栓塞,随后进行病变全切成功治愈。受此病例启发,我们还对相关文献进行了范围综述。
介绍了在我们三级医疗中心治疗的一例60岁男性右耳动静脉畸形病例,以及10篇病例报告和一项回顾性研究中描述的52例耳动静脉畸形患者。耳动静脉畸形可表现为耳部肿胀、搏动性耳鸣、疼痛和/或出血。体格检查时,可发现搏动性肿胀和/或压痛性肿块。怀疑有动静脉畸形时,应使用能最佳检测血管病变的成像方式对病变进行可视化检查,并通过栓塞、肿块切除或耳廓切除进行治疗。分析了所使用的各种诊断方法的有效性和治疗结果。
文献报道的38例病例使用了包括多普勒超声、计算机断层血管造影、磁共振血管造影和/或经股脑血管造影等多种成像方式进行诊断。另外15例未进行成像检查,仅通过体格检查和听诊确定治疗方案。在总共53例病例中,12例未接受治疗(仅观察其症状),20例接受了治疗性栓塞。总共有32例患者,包括1例未接受治疗的患者和10例先前栓塞后动静脉畸形持续或加重患者,根据病变范围接受了肿块切除或耳廓切除。未记录到重大术后并发症。术后随访时间从1个月到19年不等,仅记录到1例不可切除的残留颈面部动静脉畸形病例。
耳动静脉畸形是一种罕见疾病,但如果患者出现耳部肿胀和搏动性耳鸣,应怀疑此病。适当的成像对于疾病诊断和范围评估至关重要。由于栓塞控制效果相对较差,建议手术完全切除血管肿块。