WordNet

present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
a cardiovascular disease characterized by a saclike widening of an artery resulting from weakening of the artery wall (同)aneurism
connecting an artery to a vein; "an arteriovenous fistula"

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1. 感染性（真菌）大動脈瘤の概要 overview of infected mycotic arterial aneurysm
2. 未破裂脳動脈瘤 unruptured intracranial aneurysms
3. 胸部大動脈瘤の疫学、危険因子、病因、および自然史 epidemiology risk factors pathogenesis and natural history of thoracic aortic aneurysm
4. 膝窩動脈瘤 popliteal artery aneurysm
5. 先天性および小児冠動脈異常 congenital and pediatric coronary artery abnormalities

Wu L1, Zhao L1, Lu Y1, He L1, Hu X2.
Pediatric radiology.Pediatr Radiol.2016 Apr;46(4):541-7. doi: 10.1007/s00247-015-3497-3. Epub 2015 Dec 4.
BACKGROUND: Congenital intrahepatic shunts in children are rare and precise treatment strategies have not been established.OBJECTIVE: The purpose of this study was to present our experience with transcatheter embolization in a descriptive case series of congenital intrahepatic shunts in children.MAT
PMID 26637318

Combined surgical and endovascular treatment of complex high-flow conus medullaris arteriovenous fistula associated with Parkes Weber syndrome: case report.

Bagherpour AN1, Rodriguez GJ2, Moorthy C3, Trier TT4, Maud A2.
Journal of neurosurgery. Spine.J Neurosurg Spine.2016 Mar 25:1-5. [Epub ahead of print]
Parkes Weber syndrome (PWS) is a congenital overgrowth disorder characterized by unilateral limb and axial hypertrophy, capillary malformations of the skin, and high-flow arteriovenous fistulas (AVFs). Spinal AVFs in the setting of PWS are challenging vascular lesions that often contain multiple art
PMID 27015132

Scalp arteriovenous malformation with concomitant, flow-dependent malformation and aneurysm.

Karsy M1, Raheja A1, Guan J1, Osborn AG2, Couldwell WT3.
World neurosurgery.World Neurosurg.2016 Mar 24. pii: S1878-8750(16)00466-6. doi: 10.1016/j.wneu.2016.03.047. [Epub ahead of print]
BACKGROUND: Scalp arteriovenous malformations (sAVM) are well-described congenital abnormalities for which co-occurrence with other vascular pathologies significantly alters management strategies. The authors describe a case in which congenital sAVM was found with concomitant intracranial, flow-depe
PMID 27018012