Angiographic changes after pial synangiosis in childhood moyamoya disease

被引:1
|
作者
Robertson, RL
Burrows, PE
Barnes, PD
Robson, CD
Poussaint, TY
Scott, RM
机构
[1] CHILDRENS HOSP,MED CTR,DEPT NEUROSURG,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
moyamoya disease; children; diseases; brain; surgery;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
PURPOSE: To describe the angiographic changes accompanying the surgical treatment of moyamoya disease by pial synangiosis and to compare these changes with patient outcome; METHODS: The preoperative and postoperative cerebral angiograms, MR images, and clinical records of 13 children treated with pial synangiosis for moyamoya disease were reviewed. RESULTS: After synangiosis, 10 patients had significant neurologic improvement and three had minimal or no improvement. Postoperative MR images showed no new infarctions. Well-developed (grade A or B) transpial or transdural collaterals to the brain were present at the site of synangiosis in 84% of the surgically treated hemispheres. Cerebrovascular occlusive changes increased postoperatively in 76% of hemispheres. After synangiosis, moyamoya collaterals were increased in 48%, unchanged in 16%, and decreased in 36% of surgically treated hemispheres. All 10 patients with grade A or B collaterals bilaterally after synangiosis were asymptomatic or improved on follow-up. CONCLUSION: Pial synangiosis typically results in an increase in collaterals from the superficial temporal artery or middle meningeal artery to the brain. Synangiosis appears to result in stabilization or improvement in neurologic symptoms but does not prevent the angiographic progression of disease or the development of moyamoya collaterals. The angiographic demonstration of well-formed collaterals after synangiosis is associated with a favorable clinical outcome.
引用
收藏
页码:837 / 845
页数:9
相关论文
共 50 条
  • [1] CHILDHOOD MOYAMOYA DISEASE BEFORE AND AFTER ENCEPHALO-DURO-ARTERIO-SYNANGIOSIS - AN ANGIOGRAPHIC STUDY
    YAMADA, I
    MATSUSHIMA, Y
    SUZUKI, S
    NEURORADIOLOGY, 1992, 34 (04) : 318 - 322
  • [2] Pial synangiosis for moyamoya disease. The Bordeaux experience
    Jecko, V.
    Penchet, G.
    Champeaux, C.
    NEUROCHIRURGIE, 2016, 62 (04) : 190 - 196
  • [3] Treatment of Moyamoya Disease in the Adult Population with Pial Synangiosis
    Lin, Ning
    Aronson, Joshua P.
    Smith, Edward R.
    Scott, R. Michael
    STROKE, 2013, 44 (02)
  • [4] Treatment of moyamoya disease in the adult population with pial synangiosis
    Lin, Ning
    Aronson, Joshua P.
    Manjila, Sunil
    Smith, Edward R.
    Scott, R. Michael
    JOURNAL OF NEUROSURGERY, 2014, 120 (03) : 612 - 617
  • [5] PIAL SYNANGIOSIS FOR MOYAMOYA SYNDROME IN CHILDREN
    SCOTT, RM
    ADELSON, PD
    JOURNAL OF NEUROSURGERY, 1995, 82 (02) : A358 - A359
  • [6] PIAL SYNANGIOSIS FOR MOYAMOYA SYNDROME IN CHILDREN
    ADELSON, PD
    SCOTT, RM
    PEDIATRIC NEUROSURGERY, 1995, 23 (01) : 26 - 33
  • [7] Surgical Revascularization for Children with Moyamoya Disease: A New Modification to the Pial Synangiosis
    Chen, Chuan
    Wang, Hui
    Hou, Bo
    Luo, Lun
    Guo, Ying
    WORLD NEUROSURGERY, 2018, 110 : E203 - E211
  • [8] ANGIOGRAPHIC STUDY OF MOYAMOYA DISEASE AFTER ENCEPHALO-DURO-ARTERIO-SYNANGIOSIS (EDAS)
    YAMADA, I
    OKADA, Y
    SATOH, S
    SUZUKI, S
    MATSUSHIMA, Y
    NEURORADIOLOGY, 1987, 29 (06) : 602 - 603
  • [9] Moyamoya Disease in Pregnancy: Protective Effect of Cerebral Revascularization via Pial Synangiosis
    Lin, Ning
    Donoho, Daniel A.
    Yecies, Derek
    Scott, R. Michael
    Smith, Edward R.
    STROKE, 2013, 44 (02)
  • [10] Pial Synangiosis Ameliorates Movement Disorders in the Absence of Prior Stroke in Moyamoya Disease
    Greene, Stephanie
    Bansal, Lalit
    Coffman, Keith A.
    Nardone, Raffaele
    Zuccoli, Giulio
    JOURNAL OF CHILD NEUROLOGY, 2016, 31 (05) : 646 - 651