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Discovery of asymptomatic moyamoya arteriopathy in pediatric syndromic populations: radiographic and clinical progression

机译:小儿综合征群体无症状Moyamoya动脉的发现:射线照相和临床进展

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Object Limited data exist to guide management of incidentally discovered pediatric moyamoya. Best exemplified in the setting of unilateral moyamoya, in which the unaffected side is monitored, this phenomenon also occurs in populations undergoing routine surveillance of the cerebral vasculature for other conditions, such as sickle cell disease (SCD) or neurofibromatosis Type 1 (NF1). The authors present their experience with specific syndromic moyamoya populations to better characterize the natural history of radiographic and clinical progression in patients with asymptomatic moyamoya. Methods The authors performed a retrospective review of the clinical database of the neurosurgery department at Children's Hospital Boston, including both nonoperative referrals and a consecutive series of 418 patients who underwent surgical revascularization for moyamoya disease between 1988 and 2010. Results Within the period of time studied, 83 patients were asymptomatic at the time of radiographic diagnosis of moyamoya, while also having either unilateral moyamoya or moyamoya in association with either SCD or NF1. The mean age at presentation was 9.1 years (range 1–21 years), and there were 49 female (59%) and 34 male (41%) patients. The mean follow-up duration was 5.4 ± 3.8 years (mean ± SD), with 45 patients (54%) demonstrating radiographic progression and 37 (45%) becoming symptomatic within this period. Patients with SCD had the highest incidence of both radiographic (15 patients [75%]) and clinical (13 patients [65%]) progression, followed by NF1 (20 patients [59%] with radiographic progression and 15 patients [44%] with clinical progression) and patients with unilateral moyamoya (10 patients [35%] with radiographic progression and 9 patients [31%] with clinical progression). Conclusions Radiographic progression occurred in the majority of asymptomatic patients and generally heralded subsequent clinical symptoms. These data demonstrate that moyamoya is a progressive disorder, even in asymptomatic populations, and support the rationale of early surgical intervention to minimize morbidity from stroke.
机译:存在对象有限的数据,以指导偶然发现的儿科Moyamoya的管理。在单侧Moyamoya的设置中最能举例说明,其中监测未受影响的一方,这种现象也发生在血管血管系统的常规监测中进行其他条件,例如镰状细胞疾病(SCD)或神经纤维瘤病类型1(NF1)。作者提出了他们的经验,具体综合征Moyamoya群体,以更好地表征无症状Moyamoya患者的射线照相和临床进展的自然病史。方法对提交人对儿童医院波士顿神经外科部门的临床数据库进行了回顾性审查,包括非可手推荐和连续系列418名患者在1988年至2010年期间接受了Moyamoya疾病的手术血运疾病。结果在时间内研究,83名患者在Moyamoya的放射线诊断时是无症状的,同时还具有单侧Moyamoya或Moyamoya与SCD或NF1相关联。介绍的平均年龄为9.1岁(范围1-21岁),患有49名女性(59%)和34名男性(41%)患者。平均随访期为5.4±3.8岁(平均值±SD),45名患者(54%)在此期间显示放射学进展和37(45%)成为症状。 SCD患者的射线照相(15名患者[75%])和临床(13名患者[65%])进展,其次是NF1(20名患者[59%] [59%] [44%] [44%] [44%]临床进展)和单侧Moyamoya的患者(10名患者[35%],带射线照相进展和9名患者[31%],临床进展)。结论大多数无症状患者发生了射线照相进展,通常是预示着后续的临床症状。这些数据表明,Moyamoya是一种进步疾病,即使在无症状群体中,也支持早期手术干预的理由,以最大限度地减少中风的发病率。

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