Ahn Edward S, Scott R Michael, Robertson Richard L, Smith Edward R
Division of Pediatric Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Neurosurg Pediatr. 2013 Mar;11(3):313-9. doi: 10.3171/2012.11.PEDS12199. Epub 2013 Jan 4.
Chorea is a movement disorder characterized by brief, irregular, involuntary contractions that appear to flow from 1 muscle to another. There are a limited number of reports in the literature that have linked moyamoya disease and chorea. The authors describe their experience in treating moyamoya disease in patients in whom chorea developed as part of the clinical presentation.
The authors conducted a retrospective review of a consecutive series of 316 children who underwent pial synangiosis revascularization for moyamoya disease at the Boston Children's Hospital.
Of 316 surgically treated patients with moyamoya disease, 10 (3.2%; 6 boys and 4 girls) had chorea as a part of their presentation. The average age at surgical treatment was 9.9 years (range 3.8-17.9 years). All patients had evidence of hypertrophied lenticulostriate collateral vessels through the basal ganglia on preoperative angiography and/or MRI on affected sides. Two patients had cystic lesions in the basal ganglia. Nine patients underwent bilateral craniotomies for pial synangiosis, and 1 patient underwent a single craniotomy for unilateral disease. Follow-up was available in 9 patients (average 50.1 months). The mean duration of chorea was 1.36 years (range 2 days to 4 years), with resolution of symptoms in all patients. One patient developed chorea 3 years after surgical treatment, 4 patients had transient chorea that resolved prior to surgery, and 5 patients experienced resolution of the chorea after surgery (average 13 months).
The authors describe children with moyamoya disease and chorea as part of their clinical presentation. The data suggest that involvement of the basal ganglia by the hypertrophied collateral vessels contributes to the development of chorea, which can wax or wane depending on disease stage or involution of the vessels after revascularization surgery. In most patients, however, the chorea improves or disappears about 1 year after presentation.
舞蹈症是一种运动障碍,其特征为短暂、不规则的不自主收缩,这些收缩似乎从一块肌肉蔓延至另一块肌肉。文献中仅有少数报告将烟雾病与舞蹈症联系起来。作者描述了他们在治疗以舞蹈症作为临床表现一部分的烟雾病患者方面的经验。
作者对在波士顿儿童医院因烟雾病接受软脑膜血管吻合术血管重建的316例连续儿童病例进行了回顾性研究。
在316例接受手术治疗的烟雾病患者中,10例(3.2%;6例男孩和4例女孩)以舞蹈症作为其临床表现的一部分。手术治疗时的平均年龄为9.9岁(范围3.8 - 17.9岁)。所有患者在术前血管造影和/或患侧MRI上均有通过基底节的豆纹状侧支血管增粗的证据。2例患者在基底节有囊性病变。9例患者接受了双侧开颅软脑膜血管吻合术,1例患者因单侧疾病接受了单侧开颅手术。9例患者获得了随访(平均50.1个月)。舞蹈症的平均持续时间为1.36年(范围2天至4年),所有患者症状均缓解。1例患者在手术治疗3年后出现舞蹈症,4例患者有短暂舞蹈症,在手术前缓解,5例患者术后舞蹈症缓解(平均13个月)。
作者描述了以舞蹈症作为临床表现一部分的烟雾病患儿。数据表明,增粗的侧支血管累及基底节导致舞蹈症的发生,舞蹈症可根据疾病阶段或血管重建手术后血管的消退而加重或减轻。然而,在大多数患者中,舞蹈症在出现后约1年改善或消失。