1.Moyamoya Syndrome Caused by Paroxysmal Nocturnal Hemoglobinuria.
Zhi-Juan CHENG ; Yao-Yao SHEN ; Ishak Mohamed WARSAME ; Ting-Min DAI ; Jiang-Long TU
Chinese Medical Journal 2018;131(23):2874-2876
Adult
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Hemoglobinuria, Paroxysmal
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complications
;
pathology
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Humans
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Male
;
Moyamoya Disease
;
diagnosis
;
etiology
;
pathology
;
Young Adult
2.Systemic Lupus Erythematosus Associated with Familial Moyamoya Disease.
Chang Min LEE ; Sang Yeob LEE ; Seung Hoon RYU ; Sung Won LEE ; Kyung Won PARK ; Won Tae CHUNG
The Korean Journal of Internal Medicine 2003;18(4):244-247
We report on a 13-year-old female with systemic lupus erythematosus (SLE) who exhibited symptoms of severe migraine and familial moyamoya disease. Cerebral magnetic resonance angiography (MRA) showed stenosis and occlusion of the bilateral internal carotid arteries associated with the development of collateral circulation (moyamoya vessels). In a child, as in this case, headaches with cerebral infarction associated with moyamoya disease are unusual. Few cases of SLE associated with familial moyamoya disease have been reported, with no previous reports of such cases from Korea. There were no evidences of antiphospholipid syndrome, and activity of SLE or other risk factors for cerebral occlusion were also absent.
Adolescent
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Carotid Artery, Internal/pathology
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Female
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Human
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Lupus Erythematosus, Systemic/*complications
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Magnetic Resonance Angiography
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Migraine/etiology
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Moyamoya Disease/*diagnosis/*genetics
3.MR imaging findings of moyamoya disease.
Kee Hyun CHANG ; Jeong Geun YI ; Moon Hee HAN ; In One KIM
Journal of Korean Medical Science 1990;5(2):85-90
The brain MR images of 23 patients with angiographically proved moyamoya disease were reviewed to evaluate the capability of MR to demonstrate vascular and parenchymal abnormalities. All the MR images were obtained on a 2.0 T superconducting system and included T1-weighted sagittal and T2-weighted axial images without implementation of flow compensation (FC). The vascular abnormalities demonstrated on MR images were narrowing of the cavernous internal carotid artery (ICA) (73%), narrowing or occlusion of the supraclinoid ICA (87%) and proximal middle cerebral artery (MCA) (91%), and multiple collateral vessels in the basal ganglia and/or thalamus (96%). The parenchymal abnormalities included ischemic infarctions (74%), predominantly located in watershed areas, hemorrhagic infarctions (26%), intracerebral hematomas (13%), and intraventricular hemorrhage (13%). In conclusion, MR imaging was a useful diagnostic modality for detecting both vascular and parenchymal abnormalities associated with moyamoya disease. This may obviate the need for invasive angiography as far as the diagnosis is wanted at the non-quantitative level.
Adolescent
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Adult
;
Basal Ganglia/pathology/radiography
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Carotid Artery, Internal/pathology/radiography
;
Cerebral Angiography
;
Child
;
Female
;
Hematoma/complications/diagnosis/pathology
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Moyamoya Disease/complications/*diagnosis/pathology
;
Myocardial Infarction/complications/diagnosis/pathology