Outcome of Microsurgical Revascularization in Patients with Moyamoya Disease; First Report from Iranian Population.
نویسندگان
چکیده
AIM The aim of this study was to report the outcome of microsurgical revascularization in patients with moyamoya disease in Southern Iran. MATERIAL AND METHODS This cross-sectional study was conducted in Southern Iran during a 7-year period from 2009 to 2016. All the patients with moyamoya disease (confirmed with digital substraction angiography) who underwent microsurgical revascularization (extracranial-intracranial bypass or synangiosis) were included. All the patients were followed for at least 1 year and the outcome was measured using Glasgow outcome scale (GOS) and modified Rankin scale (MRS). RESULTS Overall we included 13 patients with 14 involved hemispheres undergoing direct and indirect revascularization. The mean age of the patients was 20.6 ± 17.5 (ranging from 0.5 to 55) years and there were 5 (38.4%) males and 8 (61.6%) females among the patients. We did not have any unfavorable outcome defined as mortality and persistent vegetative state. We performed 12 (85.7%) STA-MCA bypass and 2 (14.3%) EMS. The symptoms improved in 7 (53.8%) patients and remained as preoperative course in 5 (38.5%) patients. Only 1 (7.7%) patient developed immediate postoperative vasospasm and brain swelling who was managed successfully with decompressive craniectomy and subsequent cranioplasty (GOS=5, MRS=0). CONCLUSION This is the first study to report the safety, efficacy and outcome of the direct (STA-MCA bypass) and indirect (EMS) revascularization in patients with MMD in the Iranian population. As the prevalence of MMD is low in Iranian population, the experience and technique remains in its infancy and further advancements in the field is required.
منابع مشابه
Moyamoya Disease in an 18-Month-Old Female Caucasian Complicated by Cerebral Hyperperfusion Syndrome Following Indirect Revascularization
BACKGROUND Cerebral hyperperfusion syndrome is a rare complication of indirect revascularization due to moyamoya disease, but has not been reported previously in the pediatric population. We present a case of an 18-month-old girl with moyamoya disease that was treated with bilateral pial synangiosis and had complications consistent with cerebral hyperperfusion syndrome. This case report discuss...
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ورودعنوان ژورنال:
- Turkish neurosurgery
دوره شماره
صفحات -
تاریخ انتشار 2017