Matsumoto Shinichi, Yamamoto Yuki, Fujita Koji, Miyamoto Ryosuke, Koizumi Hidetaka, Tateishi Akihiro, Yamada Naoaki, Izumi Yuishin
Department of Neurology, Osaka Neurological Institute.
Department of Clinical Neuroscience, Tokushima University.
Surg Neurol Int. 2022 Apr 15;13:155. doi: 10.25259/SNI_173_2022. eCollection 2022.
Dystonia is a rare movement disorder with some cases being difficult to treat. Although dystonia can occur as a symptom of moyamoya disease, few studies have reported truncal dystonia occurring with middle cerebral artery (MCA) stenosis. Here, we report a case of truncal dystonia with MCA occlusion.
The patient was a 48-year-old female clerical worker who lived alone. An abnormal cervical posture initially appeared 7 years before (right flexion). Symptoms improved with medication and botulinum toxin injection. Five years before this report, her symptoms worsened, so the dose of oral medication was increased and botulinum treatment was performed, but the symptoms did not improve. The patient showed decreased cerebral blood flow (CBF) in the cortical areas but not in the basal ganglia. We performed superficial temporal artery-MCA bypass surgery because we believed that the dystonia was due to right MCA stenosis. The patient's symptoms improved immediately after surgery, except for her mild cervical backbend. Seven months after the surgery, the patient's involuntary movements showed further improvement, and symptoms have not worsened even after 2 years.
Revascularization therapy improved CBF and truncal dystonia and could be a viable treatment option for dystonia with ischemia in the MCA region. Extensive cerebral ischemia can result in cortical inhibition loss or over-adapted cerebral plasticity and cause dystonia. Revascularization therapy may be useful for patients with dystonia and decreased CBF in the MCA region.
肌张力障碍是一种罕见的运动障碍,部分病例难以治疗。尽管肌张力障碍可作为烟雾病的症状出现,但很少有研究报道大脑中动脉(MCA)狭窄伴发躯干肌张力障碍。在此,我们报告一例MCA闭塞伴发躯干肌张力障碍的病例。
患者为一名48岁的女性文职人员,独居。异常的颈部姿势最初出现在7年前(右侧屈曲)。症状通过药物治疗和肉毒杆菌毒素注射有所改善。在本报告前5年,她的症状恶化,因此增加了口服药物剂量并进行了肉毒杆菌治疗,但症状并未改善。患者皮质区域脑血流量(CBF)降低,但基底神经节未出现这种情况。由于我们认为肌张力障碍是由右侧MCA狭窄所致,故进行了颞浅动脉-MCA搭桥手术。术后患者症状立即改善,仅遗留轻度颈后伸。术后7个月,患者的不自主运动进一步改善,且2年后症状未再恶化。
血运重建治疗改善了CBF和躯干肌张力障碍,对于MCA区域缺血性肌张力障碍可能是一种可行的治疗选择。广泛的脑缺血可导致皮质抑制丧失或大脑可塑性过度适应,进而引起肌张力障碍。血运重建治疗可能对MCA区域CBF降低的肌张力障碍患者有用。