Development of moyamoya arteriopathy following treatment of intracranial tumors: clinical and radiographic characterization

Author:

Lee Jong Seok1,Storey Armide2,Lanpher Arianna3,Smith Edward R.4

Affiliation:

1. Department of Neurosurgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea;

2. Department of Obstetrics and Gynecology, Boston University School of Medicine, Boston, Massachusetts;

3. Department of Physical Medicine and Rehabilitation, University of Utah Health, Salt Lake City, Utah; and

4. Department of Neurosurgery, Boston Children’s Hospital, Boston, Massachusetts

Abstract

OBJECTIVE Moyamoya arteriopathy can develop in patients with brain tumors, particularly when associated with neurofibromatosis type 1 (NF1) or cranial irradiation. The present study aimed to analyze the clinical outcomes of moyamoya after brain tumor treatment and elucidate the effect of revascularization on brain tumors. METHODS The authors retrospectively reviewed clinical and radiographic findings in 27 patients with brain tumors who developed moyamoya requiring revascularization surgery between January 1985 and June 2017 at a single institution. The long-term clinical and neuroimaging-based outcomes were analyzed. RESULTS Among 27 patients, 22 patients underwent radiotherapy, and 12 patients had NF1. The mean ages at diagnosis of brain tumors and moyamoya were 4.4 years and 10.3 years, respectively. The mean interval between radiotherapy and moyamoya diagnosis was 4.0 years. The mean follow-up period after revascularization surgery was 8.5 years. Among 46 affected hemispheres in 27 patients, the patients who underwent radiotherapy (30 hemispheres in 22 patients) had a higher incidence of Suzuki stage 5 or 6 (20% [6/30] vs 0% [0/8]) and infarction (63.6% [14/22] vs 0% [0/5]) compared with patients without radiotherapy (8 hemispheres in 5 patients). After revascularization, stroke occurred in 4 patients, and 6 hemispheres showed Matsushima grade C, all of which occurred in patients with a history of radiotherapy. The residual brain tumors progressed in 4 of 21 patients (19%) after revascularization, comparable to the progression rates of brain tumors without revascularization in previous literature. CONCLUSIONS Patients with brain tumors can develop moyamoya that exhibits characteristic clinical and radiographic features of idiopathic MMD. Moyamoya associated with cranial irradiation has a higher incidence of stroke with less capacity for revascularization, requiring thorough evaluations and timely treatment. Revascularization does not appear to have any effect on the progression of existing brain tumors.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Reference27 articles.

1. Childhood moyamoya disease and moyamoya syndrome: a pictorial review;Currie S,2011

2. Moyamoya vasculopathy: cause, clinical manifestations, neuroradiologic features, and surgical management;Velo M,2022

3. Spontaneous occlusion of the circle of Willis in children: pediatric moyamoya summary with proposed evidence-based practice guidelines;Smith ER,2012

4. Management of stroke in neonates and children: a scientific statement from the American Heart Association/American Stroke Association;Ferriero DM,2019

5. Moyamoya syndrome: a window of moyamoya disease;Phi JH,2015

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