A case report of moyamoya disease in children treated with encephalo-duro-myo-arterio-pericranial synangiosis

Authors

  • Julius July Department of Neurosurgery, Faculty of Medicine, Universitas Pelita Harapan, Tangerang, Indonesia; Neuroscience Center, Siloam Hospital, Tangerang, Indonesia https://orcid.org/0000-0002-1106-0864

DOI:

https://doi.org/10.13181/mji.cr.204452

Keywords:

encephalo-duro-myo-arterio-pericranial synangiosis, moyamoya disease, stroke, surgery, transient ischemic attack
Abstract viewed: 1457 times
PDF downloaded: 815 times
HTML downloaded: 326 times
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Abstract

Moyamoya disease that manifests during childhood may pose a special challenge for surgeons. We report a case of a 10-year-old girl who suffered from moyamoya disease and was successfully treated with encephalo-duro-myo-arterio-pericranial synangiosis (EDMAPS). She presented with a recurrent transient ischemic attack that worsened for 1 year. She was aphasic globally (sensory and motor) and had slightly weak right extremities. Her magnetic resonance angiography and computed tomography angiography showed the typical features of moyamoya disease with bilateral stenosis at the terminal internal carotid artery, bilaterally abnormal vascular networks, and a left ischemic event involving the temporoparietal region. She was recovered well after underwent bilateral EDMAPS, fully regained her language function after 3 months, and gathered her strength back. Therefore, EDMAPS could be a good, safe, and effective treatment for moyamoya disease in children.

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References

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Published

2021-05-11

How to Cite

1.
July J. A case report of moyamoya disease in children treated with encephalo-duro-myo-arterio-pericranial synangiosis. Med J Indones [Internet]. 2021May11 [cited 2024Dec.31];30(3):228-31. Available from: https://mji.ui.ac.id/journal/index.php/mji/article/view/4452

Issue

Section

Case Report/Series
Abstract viewed = 1457 times
PDF downloaded = 815 times HTML downloaded = 326 times EPUB downloaded = 230 times