Clarity Amidst the Smoke: Moyamoya Disease, a Diagnosis Not to Be Missed
Sharifa Alnaqeeb, Diana Kheder, Noor A Abotaiban

TL;DR
This paper presents a case of moyamoya disease in a 33-year-old woman, highlighting the importance of early diagnosis and surgical treatment.
Contribution
The novelty lies in the detailed clinical presentation and neuroimaging findings of moyamoya disease in a young adult from the Philippines.
Findings
The patient exhibited acute hemiparesis and a history of TIAs, consistent with moyamoya disease.
Neuroimaging confirmed ICA, MCA, and ACA occlusion with collateral vessel formation.
The patient was successfully referred for surgical revascularization.
Abstract
Moyamoya disease (MMD) is a rare, progressive cerebrovascular disorder characterized by the bilateral stenosis of the internal carotid artery (ICA) and its proximal vessels, leading to the formation of compensatory smoke-like collateral vessels. This report describes the case of a 33-year-old Philippine woman who presented with acute right-sided hemiparesis and had a history of recurrent transient ischemic attacks (TIAs) with similar symptoms. Neuroimaging revealed intracranial hemorrhage and characteristic bilateral occlusion of the internal carotid artery (ICA), middle cerebral artery (MCA), and anterior cerebral artery (ACA) with collateral vessel formation, indicative of moyamoya disease. The patient was referred for surgical revascularization.
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Taxonomy
TopicsMoyamoya disease diagnosis and treatment · Neurological Complications and Syndromes · Cardiovascular Issues in Pregnancy
