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新生儿硬脑膜动静脉畸形表现为心力衰竭

Dural arteriovenous malformation presenting as cardiac failure in a neonate.

作者信息

Chan S T, Weeks R D

机构信息

Department of Neurosurgery, University Hospital of Wales, Cardiff, U.K.

出版信息

Acta Neurochir (Wien). 1988;91(3-4):134-8. doi: 10.1007/BF01424569.

Abstract

Dural arteriovenous malformation (AVM) is a rare clinical entity, presenting most commonly in adult patient with pulsatile tinnitus or haemorrhage. We report a case of a neonate with a massive dural arteriovenous malformation (AVM) with signs of cardiac failure soon after birth. The diagnosis was first suggested during angiocardiography when a hypertrophied left common carotid artery was detected. The AVM was supplied by branches from the left external carotid artery and the left veretebral artery and drained into the left transverse sinus near the torcula. This was excised in two stages. Post-operative angiography showed no residual malformation. The patient was well and developing normally 4 years after surgery. Review of the literature showed only 2 similar cases of dural AVM presenting in the neonatal period, both patients died, reflecting the high risks involved and the difficulties encountered in the management. Ligation of arterial supplies can be a useful temporary procedure in these high risk babies. Definitive excision should be performed later when the baby grows stronger.

摘要

硬脑膜动静脉畸形(AVM)是一种罕见的临床病症,最常见于成年患者,表现为搏动性耳鸣或出血。我们报告一例新生儿患有巨大硬脑膜动静脉畸形(AVM),出生后不久即出现心力衰竭体征。诊断最初是在心血管造影检查时提出的,当时发现左颈总动脉肥厚。该AVM由左颈外动脉和左椎动脉的分支供血,并引流至窦汇附近的左横窦。分两期进行了切除。术后血管造影显示无残留畸形。术后4年,患者情况良好,发育正常。文献回顾显示,仅有2例类似的新生儿期硬脑膜AVM病例,两名患者均死亡,这反映出此类病例的高风险以及治疗中遇到的困难。对于这些高危婴儿,结扎动脉供血可能是一种有用的临时措施。待婴儿长大后身体更强壮时,应进行确定性切除。

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