Twig-Like Middle Cerebral Artery: Acquired Lesion Rather than Congenital Anomalyopen access
- Authors
- Park, Yung-ki; Yoon, Byulhee; Hwang, Eui-hyun; Kim, Jae-hoon; Kang, Hee-in; Won, Yu-deok; Cheong, Jin-whan
- Issue Date
- Jan-2026
- Publisher
- 대한신경외과학회
- Keywords
- Angiogenesis; Middle cerebral artery; Moyamoya disease; Stroke; Twig-like
- Citation
- Journal of Korean Neurosurgical Society, v.69, no.1, pp 51 - 60
- Pages
- 10
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- Journal of Korean Neurosurgical Society
- Volume
- 69
- Number
- 1
- Start Page
- 51
- End Page
- 60
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210900
- DOI
- 10.3340/jkns.2025.0059
- ISSN
- 2005-3711
1598-7876
- Abstract
- Objective: A twig-like middle cerebral artery (T-MCA) is a rare condition characterized by steno-occlusion of the M1 segment of the middle cerebral artery (MCA) with nearby collateral arterial networks. Despite unclear pathophysiology, it is often classified as a congenital anomaly caused by failure of fusion of the plexiform MCA arterial plexus. We aimed to improve understanding of the pathophysiology of T-MCAs by analyzing incidental T-MCA findings and their natural history. Methods: A retrospective chart review was performed between January 2011 and December 2023 at three medical centers treating both ischemic and hemorrhagic strokes. Patients with suspected MCA lesions were selected through radiology reports from computed tomography, magnetic resonance angiography, and digital subtraction imaging. Results: We identified 51 T-MCA cases from a radiology report search spanning 13 years across three medical centers. The study included 9875 patients with ischemic stroke and 2097 with hemorrhagic stroke. Of the 51 T-MCA cases, incidental findings accounted for 25 (49.0%), ischemic stroke for 18 (35.3%), and hemorrhagic strokes accounted for eight cases (15.7%). T-MCA related ischemic and hemorrhagic strokes accounted for 0.18–0.38% of all strokes. The RNF213.R4810K mutation was identified in seven of 15 patients (46.7%) tested. We found three cases of a de-novo T-MCA that progressed from a normal MCA architecture. Conclusion: T-MCAs may represent an acquired secondary anomaly rather than a congenital lesion, followed by steno-occlusion of the focal MCA with new arterial network formation. Both Moyamoya angiopathy and chronic atherosclerosis likely contributed to disease progression. Formation of a microaneurysm, dilatation of the lenticulostriate artery, and hemodynamic stress can lead to stroke.
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