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头皮动静脉畸形:病例报告及文献复习

Arteriovenous malformation of the scalp: case report and review of the literature.

作者信息

Matsushige Toshinori, Kiya Katsuzo, Satoh Hideki, Mizoue Tatsuya, Kagawa Kota, Araki Hayato

机构信息

Department of Neurosurgery, Hiroshima Prefectural Hospital, Hiroshima, Japan.

出版信息

Surg Neurol. 2004 Sep;62(3):253-9. doi: 10.1016/j.surneu.2003.09.033.

Abstract

BACKGROUND

Arteriovenous malformations (AVMs) of the scalp are relatively rare, and their precise natural course remains to be elucidated. We encountered a patient with a scalp AVM that progressively enlarged over the course of 3 years by capturing feeders from intracranial arteries. To our knowledge, ours is the first serial angiographic depiction of the growth of a scalp AVM and the development of a de novo aneurysm in the superior temporal artery (STA) that performed as a feeder.

CASE DESCRIPTION

This 21-year-old female consulted us in 1998 complaining of right tinnitus and a pulsating mass in the retroauricular region. The initial angiogram revealed an AVM in the right temporo-parietal subcutaneous space with feeders from the STA, an occipital artery, a posterior auricular artery, and a middle meningeal artery (MMA). Three years later, she complained of enlargement of the lesion, increased tinnitus, and alopecia. Repeat angiographic study revealed the presence of a nidus and the appearance of new feeders from a contralateral MMA and an ipsilateral middle cerebral artery; there was a de novo saccular aneurysm in the right STA. On the day preceding surgery, the left MMA was embolized to control intraoperative bleeding. The AVM was removed totally without any dermal complications.

CONCLUSION

This case suggests that scalp AVMs can become enlarged by capturing subcutaneous or intracranial feeders, and that the consequent hemodynamic stress may induce de novo aneurysms in scalp AVMs. Capillary endothelial cells were strongly immunostained for vascular endothelial growth factor.

摘要

背景

头皮动静脉畸形(AVM)相对罕见,其确切的自然病程仍有待阐明。我们遇到一名患有头皮AVM的患者,该病变在3年的病程中通过捕获颅内动脉的供血支而逐渐增大。据我们所知,我们首次通过系列血管造影描绘了头皮AVM的生长以及作为供血支的颞浅动脉(STA)中新生动脉瘤的形成。

病例描述

该21岁女性于1998年前来就诊,主诉右耳鸣及耳后区域有搏动性肿块。初始血管造影显示右颞顶皮下间隙存在一个AVM,其供血支来自STA、枕动脉、耳后动脉和脑膜中动脉(MMA)。三年后,她主诉病变增大、耳鸣加重及脱发。重复血管造影研究显示存在一个病灶,且出现了来自对侧MMA和同侧大脑中动脉的新供血支;右STA出现了一个新生囊状动脉瘤。在手术前一天,对左侧MMA进行了栓塞以控制术中出血。AVM被完全切除,未出现任何皮肤并发症。

结论

该病例提示头皮AVM可通过捕获皮下或颅内供血支而增大,且由此产生的血流动力学压力可能诱发头皮AVM中出现新生动脉瘤。毛细血管内皮细胞对血管内皮生长因子呈强免疫染色。

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