Moyamoya disease (MMD) is a relatively rare, progressively worsening steno-occlusive condition primarily characterized by a progressive narrowing of the intracranial arteries, causing hypoperfusion and consequent cerebral ischemia and infarction. This case report discusses the rare presentation of a patient who was known to have sickle cell disease and MMD. Various investigations have revealed a typical presentation of such a disease through radiological findings. Our report highlights this rare disease and its possible association with other comorbidities, as well as the medical treatment options that patients may undergo with the option of surgical treatment.
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Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA
Isfahan Univ Med Sci, Dept Radiol & Intervent Neuroradiol, Esfahan, IranJohns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA
Shafaat, Omid
Sotoudeh, Houman
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Univ Alabama Birmingham, Dept Radiol, Div Neuroradiol, 619 19th St S, Birmingham, AL 35294 USAJohns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA
Sotoudeh, Houman
Zandifar, Alireza
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Isfahan Univ Med Sci, Dept Neurol & Intervent Neuroradiol, Esfahan, IranJohns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA
Zandifar, Alireza
Chapman, Philip R.
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Univ Alabama Birmingham, Dept Radiol, Div Neuroradiol, 619 19th St S, Birmingham, AL 35294 USAJohns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA
Chapman, Philip R.
Roberson, Glenn H.
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Univ Alabama Birmingham, Dept Radiol, Div Neuroradiol, 619 19th St S, Birmingham, AL 35294 USAJohns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, 1800 Orleans St, Baltimore, MD 21287 USA