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Research Progress of Moyamoya Disease in Children
Jianmin Piao1, Wei Wu1, Zhongxi Yang1
1Department of Neurosurgery, First Hospital of Jilin University, Changchun, 130021, P.R. China.
Insights
Moyamoya disease (MMD) in children requires early intervention due to risks of irreversible nerve damage. Combined surgical approaches offer the best prognosis for pediatric MMD patients.
Area of Science:
- Neurology
- Pediatric Neurology
- Vascular Neurology
Background:
- Moyamoya disease (MMD) involves progressive intracranial artery occlusion and compensatory vessel formation.
- Pediatric MMD presents distinct clinical features, primarily ischemia, differing from adult MMD's bleeding symptoms.
- Children face the highest risk for MMD, with earlier onset correlating to poorer prognosis.
Purpose of the Study:
- To highlight the distinct clinical features and prognosis of pediatric Moyamoya disease.
- To emphasize the critical need for early diagnosis and treatment in children with MMD.
- To review current surgical treatment strategies for Moyamoya disease in pediatric patients.
Main Methods:
- Review of indirect surgical techniques: multiple burr-hole surgery (MBHS), encephalomyosynangiosis (EMS), and encephaloduroarteriosynangiosis (EDAS).
- Review of direct surgical techniques: superficial temporal artery-middle cerebral artery (STA-MCA) anastomosis.
- Discussion of combined indirect and direct surgical approaches for pediatric MMD.
Main Results:
- Indirect surgeries demonstrate efficacy in treating pediatric MMD.
- Optimal treatment for pediatric MMD involves a combination of indirect and direct surgical procedures.
- Adequate treatment can lead to satisfactory outcomes in children with Moyamoya disease.
Conclusions:
- Pediatric Moyamoya disease necessitates specialized management due to its unique presentation and potential for severe neurological impairment.
- A combined surgical strategy is recommended for optimal treatment outcomes in children.
- Early and adequate intervention is crucial for improving the prognosis of Moyamoya disease in pediatric patients.
Abstract:
During the onset of Moyamoya disease (MMD), progressive occlusion occurs at the end of the intracranial internal carotid artery, and compensatory net-like abnormal vessels develop in the skull base, generating the corresponding clinical symptoms. MMD can affect both children and adults, but MMD in pediatric patients exhibits distinct clinical features, and the treatment prognoses are different from adult patients. Children are the group at highest risk for MMD. In children, the disease mainly manifests as ischemia, while bleeding is the primary symptom in adults. The pathogenesis of MMD in children is still unknown, and some factors are distinct from those in adults. MMD in children could result in progressive, irreversible nerve functional impairment, and an earlier the onset corresponds to a worse prognosis. Therefore, active treatment at an early stage is highly recommended. The treatment methods for MMD in children mainly include indirect and direct surgeries. Indirect surgeries mainly include multiple burr-hole surgery (MBHS), encephalomyosynangiosis (EMS), and encephaloduroarteriosynangiosis (EDAS); direct surgeries mainly include intra- and extracranial vascular reconstructions that primarily consist of superficial temporal artery-middle cerebral artery (STA-MCA) anastomosis. Indirect surgery, as a treatment for MMD in children, has shown a certain level of efficacy. However, a standard treatment approach should combine both indirect and direct procedures. Compared to MMD in adults, the treatment and prognosis of MMD in children has higher clinical significance. If the treatment is adequate, a satisfactory outcome is often achieved.
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