Literature DB >> 1710323

Arteriovenous malformation associated with moyamoya disease--case report.

T Okada1, Y Kida, T Kinomoto, T Sakurai, T Kobayashi.   

Abstract

The authors report a case of moyamoya disease accompanied by arteriovenous malformation (AVM). Angiography demonstrated typical moyamoya vessels on the right and early changes of moyamoya disease on the left. A small AVM in the left frontal lobe supplied by a distal branch of the middle cerebral artery (MCA) was also revealed. The AVM was surgically resected simultaneously with contralateral encephaloaponeurotic synangiosis for the moyamoya vessels. One month after surgery, left MCA occlusion at the origin occurred probably due to hemodynamic changes after the resection of the AVM.

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Year:  1990        PMID: 1710323     DOI: 10.2176/nmc.30.945

Source DB:  PubMed          Journal:  Neurol Med Chir (Tokyo)        ISSN: 0470-8105            Impact factor:   1.742


  3 in total

Review 1.  Arteriovenous malformation associated with moyamoya disease.

Authors:  T Fuse; T Takagi; T Fukushima; N Hashimoto; K Yamada
Journal:  Childs Nerv Syst       Date:  1996-07       Impact factor: 1.475

2.  Arteriovenous malformation with an occlusive feeding artery coexisting with unilateral moyamoya disease.

Authors:  Seong Hwan Ahn; In Seong Choo; Jin Ho Kim; Hoo Won Kim
Journal:  J Clin Neurol       Date:  2010-12-31       Impact factor: 3.077

3.  Cerebral arteriovenous malformation associated with moyamoya disease.

Authors:  Jung-Hoon Noh; Je Young Yeon; Jae-Han Park; Hyung Jin Shin
Journal:  J Korean Neurosurg Soc       Date:  2014-10-31
  3 in total

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