MS and Neuroimmunology Neurology Highlights

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Comprehensive vocabulary flashcards covering multiple sclerosis epidemiology, pathophysiology, diagnostic criteria, MRI findings, and pharmacological management based on the lecture notes.

Last updated 4:04 AM on 7/8/26
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25 Terms

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Periventricular white matter lesions

MS lesions that follow a specific pattern in the distribution of the venules.

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Benign MS

The classification for a patient with relapsing remitting MS with no disease activity for two years, occurring in 15%15\% of cases.

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EDSS 6

The Expanded Disability Status Scale score for an MS patient capable of walking with a cane for 100meters100\,meters.

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Optic Neuritis (MS-related)

Characterized clinically by unilateral pain with eye movement and a prolonged P100 on visual evoked latency.

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Disease Progression Indicator

Clinical or imaging evidence of MS advancement, specifically marked by cerebral atrophy.

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MS Genetic Risk (1st Degree Relatives)

The percentage of risk for a baby or dizygotic twin of an MS patient to develop the disease, estimated at 24%2-4\%.

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MS Genetic Risk (Monozygotic Twins)

The risk percentage for a monozygotic twin to develop MS if the other twin has it, estimated at 3040%30-40\%.

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Black Holes

T1 hypo-intensities on an MRI that represent edema or permanent tissue destruction in MS.

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Natalizumab (Tysapri)

A DMT that requires JC virus antibody screening due to the risk of Progressive Multifocal Leukoencephalopathy (PML).

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Teriflunomide

An MS medication that inhibits pyrimidine synthesis and is known to cause paresthesia as a side effect.

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Dalfampridine

A medication used to improve gait in MS patients, which is contraindicated in those with a history of seizures.

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Ocrelizumab

A disease-modifying therapy (DMT) for MS that functions through a CD20 mechanism of action.

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Alemtuzumab

A DMT targeting CD52 that can result in side effects such as hyperthyroidism and low platelet counts (30×109/L30\times 10^9/L).

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Fingolimod

A sphingosine-1-phosphate (S1P) receptor modulator that can cause a rebound effect of MS activity if stopped.

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Aquaporin-4 (AQP4) antibodies

The most useful diagnostic marker for confirming a diagnosis of Neuromyelitis Optica (NMO).

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Susac Syndrome

A clinical triad consisting of hearing loss, impaired vision, and "snowball" lesions in the corpus callosum on MRI T2/FLAIR.

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ADEM (Acute Disseminated Encephalomyelitis)

A typically monophasic demyelinating condition common in children that can present with confusion or coma and bilateral white matter changes.

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Schilder Disease

A rare MS variant seen mostly in children, characterized by bilateral symmetrical demyelination and cortical blindness.

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Uhthoff Phenomenon

The temporary worsening of MS symptoms caused by the activation of unmyelinated axons, often due to heat.

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Fatigue Treatment in MS

Managed by exercise as the mainstay, or medically with Amantadine 100mg100\,mg BID or Modafinil.

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MS Tonic Spasms

Brief, intensely painful cramps precipitated by movement or touch, effectively treated with Carbamazepine.

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LETM (Longitudinally Extensive Transverse Myelitis)

A spinal cord lesion extending over 33 or more segments, which is a cardinal feature suggestive of NMO.

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CIS (Clinically Isolated Syndrome)

A single clinical episode suggestive of MS that does not yet meet the full criteria for dissemination in time.

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RIS (Radiologically Isolated Syndrome)

Incidental MRI findings suggestive of MS in a patient who has no clinical history of neurological complaints.

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Red Flags in MS Diagnosis

Clinical features that suggest a diagnosis other than MS, including bilateral INO, extensive TM, and enhancing lesions lasting more than 3months3\,months.