Literature DB >> 21121731

Patients with moyamoya disease presenting with movement disorder.

Paritosh Pandey1, Teresa Bell-Stephens, Gary K Steinberg.   

Abstract

Moyamoya disease is a rare cerebrovascular disease characterized by idiopathic bilateral stenosis or occlusion of bilateral internal carotid arteries and the development of characteristic leptomeningeal collateral vessels at the base of the brain. Typical presentations include transient ischemic attacks or stroke, and hemorrhage. Presentation with movement disorders is extremely rare, especially in the pediatric population. The authors describe the cases of 4 children with moyamoya disease who presented with movement disorders. Among 446 patients (118 pediatric) with moyamoya disease surgically treated by the senior author, 4 pediatric patients had presented with movement disorders. The clinical records, imaging studies, surgical details, and postoperative clinical and imaging data were retrospectively reviewed. The initial presenting symptom was movement disorder in all 4 patients: chorea in 2, hemiballismus in 1, and involuntary limb shaking in 1. All the patients had watershed infarcts involving the frontal subcortical region on MR imaging. Additionally, 1 patient had a ganglionic infarct. Single-photon emission computed tomography studies showed frontoparietal cortical and subcortical hypoperfusion in all patients. Three patients had bilateral disease, whereas 1 had unilateral disease. All the patients underwent superficial temporal artery-middle cerebral artery bypass. Postoperatively, all 4 patients had complete improvement in their symptoms. The SPECT scans revealed normal perfusion in 3 patients and a small residual perfusion deficit in 1. Movement disorders are a rare presenting feature of moyamoya disease. Hypoperfusion of the frontal cortical and subcortical region was seen in all patients, and the symptomatology was attributed to ischemic dysfunction and imbalance in the cortical-subcortical-ganglionic-thalamic-cortical circuitry. Combined revascularization with superficial temporal artery-middle cerebral artery bypass and encephaloduroarteriosynangiosis leads to excellent results.

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Year:  2010        PMID: 21121731     DOI: 10.3171/2010.9.PEDS10192

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  12 in total

1.  Involuntary movement in pediatric moyamoya disease patients: consideration of pathogenetic mechanism using neuroimaging studies.

Authors:  Ji Yeoun Lee; Seung-Ki Kim; Kyu-Chang Wang; Jong Hee Chae; Jung-Eun Cheon; Jung Won Choi; Ji Hoon Phi; Byung Chan Lim; Ki Joong Kim; In-One Kim; Yong Seung Hwang; Young Seob Chung
Journal:  Childs Nerv Syst       Date:  2013-12-12       Impact factor: 1.475

2.  Successful multiple burr hole openings for limb-shaking transient ischemic attack due to moyamoya disease: illustrative case.

Authors:  Yusuke Ikeuchi; Noriaki Ashida; Masamitsu Nishihara; Kohkichi Hosoda
Journal:  J Neurosurg Case Lessons       Date:  2021-09-06

3.  Reversible striatal hypermetabolism in chorea associated with moyamoya disease: a report of two cases.

Authors:  Yoshito Sugita; Takeshi Funaki; Jun C Takahashi; Yasushi Takagi; Yasutaka Fushimi; Takayuki Kikuchi; Kazumichi Yoshida; Taketo Hatano; Natsuhi Sasaki; Susumu Miyamoto
Journal:  Childs Nerv Syst       Date:  2016-05-18       Impact factor: 1.475

4.  Hemichorea-hemiballismus caused by postoperative hyperperfusion after clipping of a giant unruptured middle cerebral artery aneurysm.

Authors:  Soichi Oya; Naoaki Fujisawa; Toru Matsui
Journal:  Surg Neurol Int       Date:  2015-05-21

Review 5.  Movement Disorders Following Cerebrovascular Lesions: Etiology, Treatment Options and Prognosis.

Authors:  Do-Young Kwon
Journal:  J Mov Disord       Date:  2016-05-25

6.  Oro-mandibular dystonia in pediatric moyamoya disease: Two cases report.

Authors:  Yuichiro Koga; Daina Kashiwazaki; Emiko Hori; Naoki Akioka; Satoshi Kuroda
Journal:  Surg Neurol Int       Date:  2021-09-06

7.  Corticostriatal Hypermetabolism in Moyamoya Disease-Induced Hemichorea: Two Case Reports and a Literature Review.

Authors:  Wen-Biao Xian; Xiang-Song Zhang; Xin-Chong Shi; Gan-Hua Luo; Chang Yi; Zhong Pei
Journal:  Front Neurol       Date:  2021-06-24       Impact factor: 4.003

8.  Dystonia an unusual presentation in pediatric moyamoya disease: Imaging findings of a case.

Authors:  Suresh Kumar; Sudhir Sharma; Anupam Jhobta; Ram Gopal Sood
Journal:  J Pediatr Neurosci       Date:  2016 Apr-Jun

9.  Acute Chorea Onset after Hot Food Consumption in a Patient with Moyamoya Disease.

Authors:  Hye Young Jung; Jee Eun Lee; Ilung Kang; Yong Bang Kim; Hyung-Eun Park; Joong-Seok Kim
Journal:  J Mov Disord       Date:  2016-01-25

Review 10.  Western Moyamoya Phenotype: A Scoping Review.

Authors:  Raphael Miller; Santiago R Unda; Ryan Holland; David J Altschul
Journal:  Cureus       Date:  2021-11-22
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