Myasthenia Gravis
Dr. Bhupendra Shah
Assistant Professor
Department of Internal Medicine
Angry Young man of Bollywood
Myasthenia Gravis
• Is a neuromuscular disorder
• weakness and fatigability
• skeletal muscle
PATHOPHYSIOLOGY
• Autoimmune disease
• Anti-ACHR antibodies
• Destruction of anti-
acetylcholine receptor
• Thymus plays a role in
autoantibody formation
Clinical features
• Affect all age groups
• Peak incidence: 20-30(women), 50-60(men)
• Weakness and Fatigability on repetition
• Weakness of ocular muscles, facial muscle and
proximal muscles
• Period of relapses and remission
Bedside test for Myasthenia Gravis
ICE-PACK TEST
• Cube of ice over the eyelid for about 2
minutes improves the ptosis
Forward arm abduction test
Upward gaze test
DIAGNOSIS AND EVALUATION
• Antibodies testing: Anti-AChR antibodies
• Electrodiagnostic testing: Repeated nerve
stimulation test
DIAGNOSIS AND EVALUATION
• Anticholinesterase test:
-Edrophonium test
• 2mg iv stat followed by 8 mg IV if no
improvement
• Look the improvement in muscle strength
Differential diagnosis
Lambert-Eaton myasthenic syndrome
• Depressed level of reflex
• Dysautonomia
• Weakness improve with activities
Associated condition
• Thymic abnormalities
• Hyperthyroidism
• Rheumatoid arthritis
Treatment
ANTICHOLINESTERASE MEDICATIONS
• Pyridostigmine
• Dose: 30-60 mg
• Frequency: 3-4 times daily
Thymectomy
• Thymoma
• All generalised myasthenia gravis
Immunosupression
• Steroid:
-Prednisolone: 10-15 mg/day increase every 2-3
days by 5mg/day till marked improvement
• Mycophenolate mofetil,
azathioprine,cyclosporine, tacrolimus and
rituxumab
Plasmapheresis and IV immunoglobin
• To provide rapid improvement
Thank You

Myesthenia gravis