Endovascular Treatment for Spontaneous Vertebral Arteriovenous Fistula in Neurofibromatosis Type 1: A Case Report

2010 ◽  
Vol 5 (2) ◽  
pp. 110
Author(s):  
Yon Kwon Ihn ◽  
Won Sang Jung ◽  
Bum-Soo Kim
2021 ◽  
Vol 14 (2) ◽  
pp. e239880
Author(s):  
Toshinori Nishizawa ◽  
Takahiro Tsuchiya ◽  
Yoshihiro Terasawa ◽  
Yasuhiro Osugi

We present the case of a 47-year-old woman with neurofibromatosis type 1 (NF1) with subarachnoid haemorrhage (SAH) from the left vertebral arteriovenous fistula, along with a review of previous cases. Our patient had a family history of NF1 and presented to the emergency department with a sudden-onset severe headache and neck pain. CT scan showed SAH. CT angiography revealed a left vertebral arteriovenous fistula and an epidural haematoma. She underwent direct surgery and was discharged without neurologic deficits. To our knowledge, this is the first case of SAH caused by perimedullary drainage of a vertebral arteriovenous fistula associated with NF1. In a literature search, we identified 40 cases of vertebral arteriovenous fistula associated with NF1. The majority of vertebral arteriovenous fistulas occurred on the left side and in women. Patients with vertebral arteriovenous fistula typically experience neck pain, radiculopathy, radiculomyelopathy and bruits.


2021 ◽  
Vol 12 ◽  
Author(s):  
Yingjin Wang ◽  
Changwei Yuan ◽  
Shengli Shen ◽  
Yang Zhang ◽  
Jiayong Zhang ◽  
...  

Background: Vertebral arteriovenous fistula (AVF) associated with neurofibromatosis type 1 (NF-1) is a rare condition in the previous reports. However, whether vertebral AVF in NF-1 is congenital or NF-1 disease progression hasn't been clarified.Case Description: We reported a 48-year-old male case of vertebral AVF simultaneously combined with thoracic scoliosis and NF-1. Preoperative CT angiography showed the AVF with multiple orifices located on the vessel wall of the vertebral artery, which was proved during the procedure of endovascular treatment. By occluding the parent vertebral artery, the AVF was finally cured. Further whole-exome sequencing identified a novel germline heterozygous point nonsense mutation, c.G397T(p.E133X), in the NF1(NM_000267) gene exon4.Conclusions: From this patient, we speculate that vertebral AVF associated with NF-1 might be a congenital disease as a manifestation of mesodermal dysplasia.


2005 ◽  
Vol 14 (9) ◽  
pp. 581-586
Author(s):  
Hikari Sato ◽  
Michiya Kubo ◽  
Naoya Kuwayama ◽  
Masanori Kurimoto ◽  
Yutaka Hirashima ◽  
...  

2021 ◽  
Vol 2 (1) ◽  
pp. 61
Author(s):  
RajnishKumar Arora ◽  
SrikantKumar Swain ◽  
Poonam Sherwani ◽  
RadheyShyam Mittal

1997 ◽  
Vol 47 (3) ◽  
pp. 265-273 ◽  
Author(s):  
Robert A. Koenigsberg ◽  
Victor Aletich ◽  
Gerard Debrun ◽  
Lawrence R. Camras ◽  
James I. Ausman

2017 ◽  
Vol 11 (4) ◽  
pp. 214-219
Author(s):  
Koji Hashimoto ◽  
Kazuya Kanemaru ◽  
Hideyuki Yoshioka ◽  
Yoshihisa Nishiyama ◽  
Tsutomu Yagishita ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document