scholarly journals Novel Indirect Revascularization Technique with Preservation of Temporal Muscle Function for Moyamoya Disease Encephalo-Duro-Fascio-Arterio-Pericranial-Synangiosis: A Case Series and Technical Note

2018 ◽  
Vol 120 ◽  
pp. 168-175
Author(s):  
Kei Noguchi ◽  
Takachika Aoki ◽  
Kimihiko Orito ◽  
Soushou Kajiwara ◽  
Kana Fujimori ◽  
...  
Neurosurgery ◽  
2019 ◽  
Vol 66 (Supplement_1) ◽  
Author(s):  
Danielle DeBacker Dang ◽  
John V Dang ◽  
Duaa AbdelHameid ◽  
Seth Mansinghani ◽  
Leon E Moores

Abstract INTRODUCTION Moyamoya disease (MMD) is a rare progressive cerebral arteriopathy characterized by nonatherosclerotic steno-occlusive lesions of the Circle of Willis. Presentation in infancy is rare and usually presents with ischemic stroke. We present a 7-mo old female with bilateral MMD who presented for indirect revascularization after 2 successive strokes in multiple vascular territories. METHODS We demonstrate a novel indirect revascularization technique in infant MMD whereby the patient's multifocal ischemic burden and STA caliber precluded arterial and myosynangiosis. We instead utilized bihemispheric pericranium for revascularization of bilateral oligemic cerebrum. Through a bicoronal scalp incision and inverted T-shaped pericranial incision, large anteriorly-based pericranial flaps were applied to the exposed pial surface using bilateral hemicraniotomies. Synangiosis extended from the frontal pole into parieto-occipital territories. We additionally performed a literature search on bypass approaches used for infant MMD. RESULTS A total of 10 infant MMD cases have been reported in the literature. Our case represents the only use of a pericranial graft in an infant without a combined approach. Pial synangiosis, EDAS, and conservative management represent techniques described in this population. Two case series utilized pericranial flaps with EDAS, however, no infants were included nor did revascularization extend beyond traditional margins. Our patient remains stroke and seizure-free for at least 16-months. She is ambulating independently and meeting her pediatric milestones. CONCLUSION Indirect revascularization is favored in pediatric MMD with approaches primarily utilizing native vessel donor grafts. Bilateral revascularization is performed in a delayed, sequential fashion if indicated. Further, collateralization is limited by the anatomical graft parameters, making hemispheric pathology difficult to comprehensively treat with these approaches. Our case demonstrates the safety and efficacy of utilizing a large bihemispheric pericranial flap on its native pedicle with bilateral hemicraniotomies for revascularization of multiple cerebrovascular territories in severe infant MMD. Our technique also allows for preservation of critical native vessels should the need for reoperation arise.


2019 ◽  
Vol 34 (13) ◽  
pp. 793-800 ◽  
Author(s):  
Qian Zhang ◽  
Peicong Ge ◽  
Yonggang Ma ◽  
Dong Zhang ◽  
Rong Wang ◽  
...  

The ring-finger protein 213 ( RNF213) gene is a major susceptibility gene for moyamoya disease. The homozygote of the p.R4810K variant on RNF213 exhibits an early onset age and severe form of moyamoya disease. We report 4 unrelated pediatric moyamoya disease cases with the homozygous p.R4810K variant and the long-term surgical outcomes. Published reports on surgical outcome of moyamoya disease case with the homozygous p.R4810K variant were reviewed. Cerebral angiography revealed classic angiographic findings of moyamoya disease in 7 hemispheres of the 4 children. All patients underwent successful indirect revascularization. Abundant collateral blood flow from the external carotid arteries to the internal carotid arteries was observed in all bypass procedures by angiography. Improvements in symptoms and cerebral blood volume were observed in all patients at long-term follow-up. This report is the first case series in the literature on the surgical management of these patients. These cases highlight the effectiveness of indirect revascularization for moyamoya disease patients with the homozygous p.R4810K variant. Early diagnosis and treatment are crucial to avoid irreversible neurologic deficits in these patients.


2021 ◽  
pp. 101288
Author(s):  
Masato Tanaka ◽  
Hardik Suthar ◽  
Yoshihiro Fujiwara ◽  
Yoshiaki Oda ◽  
Koji Uotani ◽  
...  

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Akinori Okuda ◽  
Naoki Maegawa ◽  
Hiroaki Matsumori ◽  
Tomohiko Kura ◽  
Yasushi Mizutani ◽  
...  

Author(s):  
Francisco Marcó del Pont ◽  
Sebastián Juan María Giovannini ◽  
Tomás Ries Centeno ◽  
Guido Caffaratti ◽  
Emiliano Lorefice ◽  
...  

PM&R ◽  
2011 ◽  
Vol 3 ◽  
pp. S197-S197
Author(s):  
Mallikarjuna Nallegowda ◽  
Ziyad Ayyoub ◽  
Murray Brandstater ◽  
Jared Myers ◽  
Jiangnan Wang ◽  
...  

2019 ◽  
Vol 121 ◽  
pp. e70-e76 ◽  
Author(s):  
Rui Zong ◽  
Teng Li ◽  
Lenian Lu ◽  
Guangyu Qiao ◽  
Xinguang Yu

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