MYOPATHIES,MYOTONIA, CARDIOMYOPATHIES. Presenter: Dr Eva F. Mujuni (Resident-Internal Medicine)...
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Transcript of MYOPATHIES,MYOTONIA, CARDIOMYOPATHIES. Presenter: Dr Eva F. Mujuni (Resident-Internal Medicine)...
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MYOPATHIES,MYOTONIA,CARDIOMYOPATHIES.
Presenter: Dr Eva F. Mujuni (Resident-Internal Medicine)
Facilitator: Dr B.L. Mtinangi
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Overview1.Introduction2.Myopathies Definition Causes Classification Pathophysiology Clinical presentation Diagnosis Treatment
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Overview…
3.Myotonia Definition Causes Treatment
4.Cardiomyopathies Definition Causes Types Pathophysiology Clinical Presentation Diagnosis Treatment
5.References
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Myopathies
A myopathy is a muscular disease in which the muscle fibers do not function for any one of many reasons, resulting in muscular weakness.
It can occur in heart muscle, skeletal muscles, or muscles of various organs (for example, the stomach or intestines).
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Myopathies Winged scapulae
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Myopathies…
Depending on the causes Myopathies can be classified as:
GeneticInflammatoryEndocrine Toxic Idiopathic
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Myopathies…
Classification of Myopathies…
Genetic myopathies
Caused by a genetic defect. The most common muscular dystrophies, Duchenne
and Becker muscular dystrophy, result from a genetic defect on the X chromosome.
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Myopathies… Classification of Myopathies…
Other Genetic Myopathies include:
• Central core disease • Centronuclear (myotubular) myopathy • Myotonia congenita • Nemaline myopathy • Paramyotonia congenita • Periodic paralysis (hypokalemic and hyperkalemic forms) • Mitochondrial myopathies
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Myopathies… Classification of Myopathies…
Inflammatory myopathies
They are autoimmune disorders
Healthy muscle fibres are attacked by the body's immune system and become inflammed , this in turn damages the muscle.
Example in: Polymyositis (PM) Dermatomyositis (DM) is characterised by a skin rash as well as
muscle symptoms of PM
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Myopathies… Classification of Myopathies…
Endocrine myopathies
Caused by the over or underproduction of hormones.
Examples are: Hyperthyroid myopathy is caused by the thyroid gland
producing too much thyroxine. Hypothyroid myopathy is caused by the underproduction of
thyroxine.
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Myopathies… Classification of myopathies…
Endocrine myopathies…
Cushing's disease, characterized by overproduction of hormones produced by the pituitary and adrenal glands.
Excess parathyroid hormone results in hypercalcemia, which causes proximal muscle pain and weakness.
Hormone-secreting tumors can also cause endocrine disorders that cause myopathies.
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Myopathies… Classification of myopathies…
Toxic myopathies
They are caused by exposure to certain medications and chemicals.
Excessive alcohol intake . Drugs and chemicals - Anesthetics (eg. lidocaine,
mepivacaine, ethyl chloride) Cholesterol lowering medication (eg. clofibrate, genfibrozil,
lovastatin, simivastatin, niacin)
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Myopathies…
Classification of myopathies…
Toxic myopathies…
Glucocorticoids (eg. triamcinolone, dexamethasone, betamethasone)
Narcotics (eg. cocaine, heroin, meperidine) Other drugs (eg. zidovudine, D-penicillamine,
procainamide, chloroquine, gallamine) Herbicides, insecticides
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Myopathies…
Clinical Presentation of Myopathies
Symmetric proximal muscle weaknessMalaiseFatiguePatient may note dark colored urine and/or fever.No sensory complaints or paresthesias are noted with myopathies.Atrophy and hyporeflexia are very late findings in most patients with myopathy. The early presence of these findings usually implicates neuropathies.
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Myopathies…
Diagnosis of MyopathiesMedical historyThorough physical examCK with isoenzymesElectrolytes- calcium, magnesiumSerum myoglobinSerum creatinine and BUN
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Myopathies…
Diagnosis of Myopathies…Urinalysis: Myoglobinuria is indicated by
positive urinalysis with few RBCs on microscopic evaluation.
Complete blood countErythrocyte sedimentation rateThyroid function tests
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Myopathies…
Diagnosis of Myopathies…Muscle tissue biopsyElectromyogram
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Myopathies…
Treatment:Corticosteroids. Immunosuppressive drugs - cyclosporine,
tacrolimus , mycophenolate mofetil and rituximab .
Physical therapy. Treating the underlying condition
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Myotonia
A symptom of several muscular disorders characterized by:
Increased muscular irritability and contractility
Slow relaxation of the muscles after voluntary contraction or electrical stimulation.
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Myotonia…
Causes of Myotonia Abnormality in the muscle membrane—
specifically, the ion channels that controls the contraction of muscle fibers.
Examples are:myotonic muscular dystrophy myotonia congenita
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Myotonia…
Myotonia congenita This disease is caused by mutations in the
gene for a chloride channel that is necessary for shutting off the electrical excitation that causes muscle contraction.
The Becker type is inherited in an autosomal recessive pattern.
The Thomsen type is autosomal dominant.
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Myotonia…
Treatment of Myotonia Mexelitine Quinine Phenytoin Physical therapy
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Cardiomyopathies
Cardiomyopathy is a chronic disease of the heart muscle (myocardium), in which the muscle is abnormally enlarged, thickened, and/or stiffened.
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Cardiomyopathies…
Common types:
Dilated cardiomyopathy (DCM)Hypertrophic cardiomyopathy (HCM)Restrictive cardiomyopathy (RCM)
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Dilated cardiomyopathy (DCM)
Dilated cardiomyopathy is a condition characterized by dilatation and impaired systolic function of the left and/or right ventricle.
In majority,the cause is idiopathic
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DCM
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Causes of dilated cardiomyopathy
Genetic eg: Autosomal dominant DCM, X-limked cardiomyopathy
Inflammatory eg: Post-infective, autoimmune, connective tissue diseases( such as SLE and systemic sclerosis)
Metabolic eg: Glycogen storage diseasesNutritional eg: Thiamin and selenium
deficiency
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Causes of dilated cardiomyopathy…
Endocrine eg Acromegaly, Thyrotoxicosis, Diabetes mellitus
Infiltrative eg: Hereditary haemochromatosisNeuromuscular eg: Muscular dystrophy,
mitochondrial myopathiesToxic eg: Due to Alcohol,cocaine,
CyclophosphamideHaematological eg: Sickle cell anemia,
Thrombotic thrombocytopenic purpura
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DCM
Pathophysiology25% of the idiopathic cases are familialIn the majority of familial cases the
inheritence is autosomal dominantThe responsible genes are the genes encoding
cytoskeletal or associated myocyte proteins(dystrophin,actin,desmin,troponin,lamin)
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DCM
DiagnosisChest x-rayECGEchocardiographyTesting for cause as indicatedDiagnosis is by history, physical examination,
and exclusion of other common causes of ventricular failure (eg, systemic hypertension, primary valvular disorders, MI
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DCM
ManagementAnticoagulation (EF <30%, hx of embolic
events,atrial fibrillation)Limit activity based on functional statusSalt restriction Fluid restriction Medical therapy– ACE inhibitors, diuretics– Digoxin– Beta blockers
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DCM
Management…
Cardiac transplantation • This disorder is the most common indication for
cardiac transplantation
Left Ventricular Reduction Procedures• LV-reshaping
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Hypertrophic cardiomyopathy (HCM)
Hypertrophic cardiomyopathy (HCM) is a condition in which the heart muscle becomes thick.
Characterized by variable myocardial hypertrophy most commonly involving the interventricular septum
Majority of cases are familial,autosomal dominant
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HCM
With HCM, the sarcomeres (contractile elements) in the heart increase in size, which results in the thickening of the heart muscle.
In addition, the normal alignment of muscle cells is disrupted, a phenomenon known as myocardial disarray.
HCM is most commonly due to mutations in the genes encoding sarcomeric proteins.
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HCM
• Beta myosin heavy chain mutations cause elaborate ventricular hypertrophy
• Troponin mutations cause less hypertrophy but more disarray and abnormal vascular response eg.hypotension,hence liable to sudden deaths.
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HCM
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HCM
Clinical features :Asymptomatic• Echocardiographic findings only
Symptomatic• Dyspnea • Chest pain• Fatigue, pre-syncope, syncope • Palpitation, PND, CHF, dizziness• Cardiac arrythmias,Sudden death
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HCM TreatmentThe primary goal of medications is to relieve
symptoms such as chest pain, shortness of breath, and palpitations.
Beta blockers are considered first-line agents, as they can slow down the heart rate.
Nondihydropiridine calcium channel blockers such as verapamil can be used
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HCM
Treatment…
Surgical myectomyAlcohol septal ablationVentricular pacingCardiac transplantation
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Restrictive cardiomyopathies It is a disease of the myocardium characterized
by restrictive filling and reduced diastolic volume of either or both ventricles, with normal or near-normal systolic function.
May be classified as: Primary (e.g., endomyocardial fibrosis, Löffler's
endocarditis, idiopathic restrictive cardiomyopathy)
Secondary
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Restrictive cardiomyopathies
Causes of secondary restrictive cardiomyopathy include:
Infiltrative diseases (e.g., amyloidosis, sarcoidosis)
Storage diseases (e.g., hemochromatosis, glycogen storage disorders, Fabry's disease).
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Restrictive cardiomyopathies
Rigid ventricular wall with impaired ventricular filling
Much less common than DCM or HCM outside the tropics, but frequent cause of death in Africa, India, South and Central America and Asia primarily because of the high incidence of endomyocardial fibrosis in those regions
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Restrictive cardiomyopathies
The idiopathic form may be familial Associated with mutations in the sarcomeric
protein troponin I
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Restrictive cardiomyopathies
Clinical manifestations:Dyspnea Fatigue Symptoms of right and left heart failure Elevated Jugular Venous Pulse
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Restrictive cardiomyopathy
Management:
No satisfactory medical therapy .Cardiac failure should be treated.Cardiac transplantation
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References
• Kumar and Clark,Clinical Medicine 6th edition• Review of medical Physiology,W.Ganong 21st
edition• Textbook of Medical Physiology,Guyton and
Hall,10th edition• Medscape references-Drugs,diseases and
procedures• http:www.health of children.com• Wikipedia