What is the diagnosis for a 67-year-old female with a history of syncope and collapse, presenting with encephalomalacia, T2 signal hyperintensity, and susceptibility artifacts on MRI brain, suggestive of remote ischemic and/or traumatic injuries with associated superficial siderosis?

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Differential Diagnosis for MRI Brain Findings

The patient's MRI brain findings reveal several sites of encephalomalacia, T2 signal hyperintensity, and susceptibility, suggesting remote injuries, ischemic and/or traumatic, with associated superficial siderosis. Here's a categorized differential diagnosis:

  • Single most likely diagnosis
    • Chronic traumatic encephalopathy (CTE) or remote traumatic brain injury: The presence of encephalomalacia and superficial siderosis, particularly in a pattern suggesting previous trauma, makes this a strong consideration. The history of syncope and collapse could be related to the sequelae of such injuries.
  • Other Likely diagnoses
    • Multi-infarct dementia or vascular dementia: The findings of ischemic changes and encephalomalacia could indicate a history of small vessel disease or larger territorial infarcts, contributing to cognitive decline and potentially to the episodes of syncope.
    • Amyloid angiopathy: Given the patient's age and the presence of superficial siderosis, amyloid angiopathy could be a consideration, especially if there's a history of lobar hemorrhages or microbleeds.
  • Do Not Miss (ddxs that may not be likely, but would be deadly if missed.)
    • Cerebral amyloid angiopathy with associated hemorrhages: Although less likely, missing this diagnosis could be critical due to the potential for future hemorrhagic events.
    • Brain tumor (e.g., glioma, metastasis): Although the description favors chronic changes, it's crucial not to overlook the possibility of a tumor, especially if any of the lesions show atypical features or enhancement on post-contrast images.
    • Vasculitis (e.g., primary CNS vasculitis): This could present with a variety of imaging findings, including ischemic changes and hemorrhage, and is critical to diagnose due to its treatable nature.
  • Rare diagnoses
    • CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy): A hereditary condition leading to stroke and dementia, characterized by white matter changes and subcortical infarcts.
    • MELAS syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes): A mitochondrial disorder that can cause stroke-like episodes and encephalopathy, though typically presents at a younger age.
    • Susac syndrome: A rare condition characterized by microangiopathic changes in the brain, retina, and cochlea, leading to a variety of neurological symptoms.

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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