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Multiple sclerosis (MS)

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Multiple sclerosis (MS) is a chronic disease that begins most commonly in young adults and is characterized pathologically by multiple areas of central nervous ... – PowerPoint PPT presentation

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Title: Multiple sclerosis (MS)


1
Multiple sclerosis (MS)
  • is a chronic disease that begins most commonly in
    young adults and is characterized pathologically
    by multiple areas of central nervous system (CNS)
    white matter inflammation, demyelination, and
    glial scarring (sclerosis)

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Etiology
  • The cause of MS is unknown. There are 2 groups of
  • possible reasons of the disease
  • Genetic susceptibility
  • Environmental factors
  • Infections (the virus can influence on nervous
    system directly or through the autoimmune
    mechanisms).
  • Geographical (ground, water properties, the
    number of light days in a year)
  • Toxic
  • Social conditions
  • Diet (domination of meat in the diet)
  • Other factors (trauma)

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The typical features of MS pathogenesis
  • Clinical and immune signs are closely connected
    with each other in MS patients. Usually immune
    signs are the first ones
  • There is disturbance of activating and
    suppressing cytokines balance
  • The immunity is changed in the course of the
    disease
  • There are signs of immune suppression and immune
    modulation according to the stage of the disease
    exacerbation or remission

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Myelin function
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Pathology
  • There are multiple areas of Central Nervous
    System white matter inflammation, demyelination
    and glial scarring (sclerosis). The lesions are
    multiple in space. They are located in
  • spinal cord
  • cerebellum
  • Optic n.
  • brain white substance

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The beginning of the disease
  • Paresthesia. It is the feeling of numbness or
    tingling in one of the extremity. It can be
    spread during the next 3 4 days and lasts for
    about 1 2 weeks, then gradually disappear.
  • Motor disorders - weakness in lower extremities.
    This symptom is much more common at the age of 25
    40 years.
  • Retrobulbar neuritis is a progressive loss of
    vision, colour vision disturbances. It lasts for
    about several weeks.
  • Oculomotor n. disorders (diplopia and cross eye).
  • Pelvis disorders (retention of urine,
    micturition)
  • Acute vestibular syndrome
  • Cerebellar disorders ataxia, disorders of
    coordination.

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Typical clinical features
  • Motor disorders 89 97
  • Ataxia cerebellar, sensitive and vestibular
    62 74
  • Sensory disorders pains and sensitive ataxia -
    72 74
  • Brain stem symptoms vestibular syndrome,
    dysarthria, CNs lesion 47 58
  • Visual and eye movements disorders 42 52
  • Autonomic disturbances pelvic and sexual
    disorders 46 60
  • Nonspecific symptoms cognitive, memory
    disturbances, loss of attention 62
  • Paroxysmal symptoms

17
Visual field disorders of MS
18
Clinical forms
  • Cerebral
  • cortical (epileptic attacks, psychiatric
    disorders)
  • Visual
  • brain stem
  • cerebellar.
  • Spinal
  • Cervical
  • Thoracic
  • lumbar sacral
  • pseudotabes.
  • Cerebrospinal

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The course of the disease
  • Acute
  • Subacute
  • Chronic
  • remittent,
  • - remittent progressive
  • - progressive remittent
  • - progressive

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  • The periods of the disease
  • Exacerbation
  • Remission (complete, incomplete).
  • Stable period
  • MS degree
  • I, II, III, IV, V

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Scale of MS disability (EDSS)
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MS diagnosis
  • Immune examinations of blood and CSF. Usually
    there are increased Ig G, M, A contents.
  • Insignificant increasing of protein content and
    moderate pleocytosis in CSF
  • Lymphocytosis, eosynophilia in exacerbation
    stage leukopenia, lymphopenia in the period of
    remission.
  • Increased thrombocytes aggregation and fibrinogen
    content.
  • Increased Ig content in serum and decreased T
    lymphocytes quantity.

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  • To put veridical MS we have to reveal in patient
    at least 2 focuses of lesion and 2 exacerbations,
    or 2 exacerbations of 1 clinical focus and 1
    paraclinical supposed focus.
  • According to the accepted criteria there should
    be at least 3 focuses in MRI (2 of them should be
    located paraventricularly, 1 subtentorialy
    (that means in brain stem or cerebellum). The
    diameter of focuses should be at least 6 mm, or
    there should be 4 focuses, 1 of them
    periventricularly.

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MRI of MS
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MRI of MS
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Sagittal T1-weighted MRI depicts multiple
hypointense lesions in the corpus callosum this
finding is characteristic of MS
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Coronal fluid-attenuated inversion recovery
(FLAIR) MRI in a patient with multiple sclerosis
demonstrates periventricular highsignal
intensity lesions, which exhibit a typical
distribution for MS. FLAIR MRI is a highly
sensitive sequence for lesion detection,
particularly supratentorially.
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Axial T2-weighted MRI in a patient with multiple
sclerosis demonstrates numerous white matter
plaques in a callosal and pericallosal white
matter distribution.
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Spinal form of MS
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  • One of the limitations of using MRI in patients
    with MS is the discordance occurring between
    lesion location and the clinical presentation. In
    addition, depending on the number and location of
    findings, MRI can vary greatly in terms of
    sensitivity and specificity in the diagnosis of
    MS. This is especially true of primary
    progressive MS, which may not show the classic
    discrete lesions of relapsing-remitting MS.

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  • A clinician presented with an MRI report that
    details a few "nonspecific white matter lesions"
    that are "compatible with MS" is often frustrated
    with the lack of sensitivity and specificity of
    such a description. For this reason, imaging
    findings need to be described in detail, and
    preferably referenced to one of the published set
    of diagnostic criteria such as those by Paty or
    Barkhof. Finally, the specific patient's
    neurologic history and clinical findings must be
    correlated with the imaging to establish an
    accurate diagnosis

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  • Cerebrospinal fluid (CSF) analysis for
    oligoclonal banding or immunoglobulin G (IgG)
    levels is no longer routine in the investigation
    of MS, although this test may be of use when MRI
    is unavailable or MRI findings are nondiagnostic

35
Treatment
  • Pathogenetical treatment
  • Corticosteroids and ACTH
  • Cytostatics and immune modulators, non specific
    immune suppressors
  • Cytokines, interferones
  • Antigen specific immune therapy

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Corticosteroids and ACTH
  • Prednisone is used orally 1 1.5 mg/kg/day twice
    a day during 10 14 days. Then during the next 2
    months we decrease the dose gradually.
  • One of the most popular schema for
    Methylprednisolone usage is 500 1000 mg per day
    i/v in 500 ml of physiological solution during 3
    5 days. Then Prednisone is used in dose 0.5 1
    mg/kg during 3 7 days with gradually decreasing
    of dose during the next 2 3 weeks. This way of
    usage has much more expressed and quick
    effectiveness and insignificant outside effects
  • Dexamethasone is used i/v or i/m according to the
    schema 8 mg per day during 7 days, 4 mg 4
    days, 2 mg 3 days. It is used at retrobulbar
    neuritis

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The peculiarities of Corticosteroids usage
  • Long lasting and frequent usage is undesirable
  • Usually H-2 blockers are used together with
    Corticosteroids
  • ACTH has immune suppressive activity, inhibits
    cellular and humoral immunity. It is used in
    dose 40 100 U i/m during 10 14 days.
  • Plasmapheresis is used in case of exacerbation.

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Cytostatics and immune modulators, non specific
immune suppressors
  • Asatioprine, Cyclophosfamidum, Cyclosporinum A.
    But all of these medicines have a lot of outside
    effects.
  • The representatives of immune modulators are - T
    activinum, Timalinum, Myelopid, Levamisolum.
    They are prescribed at progressive forms of MS.
  • T activinum is used in dose 100 mcg s/c every
    evening during 5 days, then 1 3 injections
    every 10 days.
  • Timalinum is used in dose 10 mg i/m twice a day
    during 5 days, then every 10 days 2 injections
    are used.

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Interferones
  • There are 3 types of Interferonum a, ß, ?.
  • a - Interferonum has neither toxic nor treating
    activity.
  • ? - Interferonum activates immune system and
    thats why it provokes exacerbations.
  • ß - Interferonum inhibits production of ?
    interferonum, increases activity of T
    suppressors, has antiproliferative, antiviral and
    immune modulating properties.
  • Rebif is a modern human ß interferonum
    produced by Serono production and is used for
    MS treatment. It is used in dose 6 12 mln s/c
    three times per week. It is one of the most
    effective modern medicines in MS patients, but
    unfortunately it is very expensive

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Antigen specific immune therapy
  • One of the representatives of these medications
    is Copaxone, made in Israel. Cost of treatment is
    about 7 000 . It is used in dose 20 mg per day
    s/c during 6 24 months. It has selective immune
    modulating action.

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Acute multiple encephalomyelitis (AMEM)
  • It is an infectious allergic disease that is
    characterized by acute multiple lesion of the
    brain and spinal cord

42
Clinical forms
  • Encephalomyelopoliradiculoneuritis it is the
    most common form of the disease, which is
    characterized by the lesion of all parts of
    nervous system.
  • Polioencephalomyelitis it is characterized by
    the lesion of CNs nuclei and spinal cord gray
    substance.
  • Opticoencephalomyelitis and opticomyelitis are
    characterized by optic nerve neuritis and
    symptoms of lesion of brain and spinal cord.
  • Disseminated myelitis the spinal cord is
    damaged on different levels.

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Treatment
  • Corticoids Prednisolone and Methylprednisolone
    in dose 10 15 mg per kg i/v by drops per day.
    Later we can use it in pills - 1.5 2 mg/kg
    every other day.
  • Together with this medicine we prescribe
    anabolics , K, Ca, vitamin C.
  • In acute stage we prescribe desensibilizating and
    dehydrating medicines. In case of severe bulbar
    disorders we include resuscitation measures.
  • Plasmapheresis and vitamin B are also used.
  • In residual period we prescribe massage,
    dibasol, KJ, biostomulants, Lidasa, Seduxen,
    sanatorium treatment.

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Clinical symptoms of MS
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