Pediatric moyamoya disease: An analysis of 410 consecutive cases

Ann Neurol. 2010 Jul;68(1):92-101. doi: 10.1002/ana.21981.

Abstract

Objective: Moyamoya disease (MMD) is a cerebrovascular occlusive disease of the bilateral internal carotid arteries that causes a compensatory abnormal vascular network at the base of brain. The rare incidence and various surgical techniques applied have limited the clinical research on MMD.

Methods: We conducted a retrospective analysis of the surgical outcome of 410 pediatric MMD patients. All patients were treated in a relatively uniform scheme at a single institution. The surgical procedures consisted of bilateral encephaloduroarteriosynangiosis augmented by bifrontal encephalogaleo-/periosteal synangiosis. Logistic regression analyses were applied to reveal the prognostic factors for surgical outcome.

Results: The overall clinical outcome was excellent in 66%, good in 15%, fair in 15%, and poor in 4% of the patients. Therefore, 81% of the patients had a favorable clinical outcome (excellent and good). Multivariate analyses revealed that infarction on presentation was associated with unfavorable clinical outcome (odds ratio [OR], 2.85; 95% confidence interval [CI], 1.49-5.46; p < 0.01) and decreased vascular reserve only on single-photon emission computerized tomography (OR, 0.07; 95% CI, 0.01-0.52; p < 0.01), with favorable clinical outcome.

Interpretation: Our results indicate that an early diagnosis and active intervention before establishment of irreversible hemodynamic change are essential to achieve a favorable clinical outcome in children with MMD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Brain / diagnostic imaging
  • Brain / pathology
  • Brain / physiopathology
  • Brain Infarction / diagnosis
  • Brain Infarction / diagnostic imaging
  • Brain Infarction / surgery
  • Cerebral Arteries / pathology
  • Cerebral Arteries / physiopathology
  • Child
  • Child, Preschool
  • Early Diagnosis
  • Female
  • Follow-Up Studies
  • Humans
  • Infant
  • Male
  • Moyamoya Disease / diagnosis*
  • Moyamoya Disease / diagnostic imaging
  • Moyamoya Disease / surgery*
  • Neurosurgical Procedures / methods
  • Prognosis
  • Radionuclide Imaging
  • Retrospective Studies
  • Treatment Outcome