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伴颅内延伸的头皮动静脉畸形的诊断与治疗

Diagnosis and Treatment of Scalp Arteriovenous Malformations With Intracranial Extension.

作者信息

Kanth Aditi M, Ricci Joseph A, Adetayo Oluwaseun A

机构信息

Division of Plastic Surgery, Albany Medical Center, Albany, NY.

出版信息

J Craniofac Surg. 2019 Nov-Dec;30(8):2429-2431. doi: 10.1097/SCS.0000000000005774.

Abstract

Scalp arteriovenous malformations (AVMs) are rare entities that may present as large, tortuous vascular lesions with resultant craniofacial deformity. Radiologic findings include feeding arteries and veins associated with dilated tortuous vessels. Intracranial extension is rare. A 5-year-old African American male presented with an occipital mass presumed to be a dermoid cyst on referral. Further workup revealed the presence of a scalp AVM that demonstrated extension into the left sigmoid sinus. Radiologic and intraoperative images are presented. Literature search revealed only 4 patients with scalp AVM extending intracranially into the sagittal sinus, 2 of which were managed with coagulation and division of the feeding vessels and the other 2 underwent preoperative embolization. Our patient is the 1st to be reported to have sigmoid sinus extension. Scalp AVMs with intracranial extension are rare, and require further preoperative workup. Following ultrasound evaluation, computed tomography angiography, magnetic resonance angiography, magnetic resonance imaging, or cerebral angiography can be considered. Treatment entails resection, but preoperative embolization is increasingly used, mirroring patients without intracranial extension. Further studies are needed to evaluate the efficacy and risk profile of these treatments.

摘要

头皮动静脉畸形(AVM)是一种罕见的病变,可表现为巨大、迂曲的血管病变,并导致颅面畸形。影像学表现包括与扩张迂曲血管相关的供血动脉和静脉。颅内扩展罕见。一名5岁非裔美国男性因枕部肿块转诊,最初推测为皮样囊肿。进一步检查发现存在头皮AVM,并延伸至左侧乙状窦。本文展示了影像学及术中图像。文献检索显示,仅有4例头皮AVM颅内扩展至矢状窦,其中2例采用供血血管凝固和切断治疗,另外2例接受了术前栓塞。我们的患者是首例报道有乙状窦扩展的病例。颅内扩展的头皮AVM罕见,需要进一步的术前检查。超声评估后,可考虑进行计算机断层血管造影、磁共振血管造影、磁共振成像或脑血管造影。治疗方法为切除,但术前栓塞的应用越来越多,与无颅内扩展的患者情况相似。需要进一步研究来评估这些治疗方法的疗效和风险。

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