1.Percutaneous left atrial appendage occlusion therapy in a female recurrent ischemic stroke patient with persistent atrial fibrillation and moyamoya disease.
Song ZUO ; Jia Hui WU ; Xiao Wen BO ; Xin ZHAO ; Xu LI ; Song Nan LI ; Jian Zeng DONG ; Chang Sheng MA
Chinese Journal of Cardiology 2020;48(11):982-984
2.Off-Pump Coronary Artery Bypass Grafting in Moyamoya Disease.
Yonsei Medical Journal 2007;48(5):876-878
Moyamoya disease is an occlusive intracranial arteriopathy owing to intimal hyperplasia with formation of abnormal cerebrovascular collateral networks; however, the etiology remains unclear. Although this disease is known to be associated with renovascular hypertension, it is extremely rare for it to be associated with stenoses of the coronary arteries. We herein described a case of a 56-year-old female with angina and asymptomatic moyamoya disease. We performed off-pump coronary artery bypass grafting (OPCAB) to avoid cardiopulmonary bypass and the risk of intraoperative hypotension. Conventional coronary artery bypass grafting has a potential risk of brain ischemia in moyamoya patients, but OPCAB may avoid this perioperative cerebral ischemic complication.
*Coronary Artery Bypass, Off-Pump/adverse effects
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Coronary Stenosis/complications/surgery
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Female
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Humans
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Intraoperative Complications/prevention & control
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Middle Aged
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Moyamoya Disease/complications/*surgery
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Risk Factors
3.The Rare Association of Moyamoya Disease and Cerebral Arteriovenous Malformations: a Case Report.
Te Chang WU ; Wan Yuo GUO ; Hsiu Mei WU ; Feng Chi CHANG ; Cheng Ying SHIAU ; Wen Yuh CHUNG
Korean Journal of Radiology 2008;9(Suppl):S65-S67
A 36-year-old man was diagnosed with a right temporal lobe grade II cerebral arteriovenous malformation (cAVM) and was treated with radiosurgery. At nine months after the cAVM radiosurgery, the patient began to develop bilateral focal narrowing at the M1 segments of the bilateral middle cerebral arteries. The narrowing progressively deteriorated as was demonstrated on longitudinal serial follow-up MR imaging. X-ray angiography performed at 51 months after radiosurgery confirmed that the cAVM was cured and a diagnosis of moyamoya disease. To the best of our knowledge, this is the first case of cAVM-associated moyamoya disease that developed after radiosurgery. Given the chronological sequence of disease development and radiation dose distribution of radiosurgery, it is proposed that humoral or unknown predisposing factors, rather than direct radiation effects, are the cause of moyamoya disease associated with cAVM.
Adult
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Humans
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Intracranial Arteriovenous Malformations/diagnosis/*surgery
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Magnetic Resonance Imaging
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Male
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Moyamoya Disease/*etiology
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Postoperative Complications
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Radiosurgery