Sandbox Myopathy: Difference between revisions

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Revision as of 15:51, 3 April 2018


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Differentiating Various Muscle Weakness

Disease Symptoms History Physical

Examination

Diagnosis
Age of onset Muscle weakness Fever Muscle pain Gait abnormality Neuropathy Myoglobinuria Other features Laboratory Findings Creatine Kinase Muscle Biopsy Electromyogram
Proximal DIstal
Medications
Corticosteroids Variable + - - + - - -
  • + History of medications
  • Facial and sphincter muscles usually are spared
- - -
Statins 60+ + - - + - - -/+(rhabdomyolysis)
  • N/A
  • Positive medication history
  • Tenderness
  • Muscle aches
  • ↑↑ liver enzymes
  • ↑↑
  • Necrosis
  • Degeneration, and regeneration of fibers
  • Phagocytic infiltration
-
Chemotherapeutic -
Organophosphate intoxication -
Alcohol Variable + +
  • Change in mental status
  • Telangiectasia
  • Peripheral neuropathy
Endocrine
Cushing's disease
Adrenal insufficiency
Secondary hyperparathyroidism
Hyperthyroidism
Hypothyroidism
Inflammatory / Rheumatologic
Dermatomyositis[1]
  • 40s-50s
  • Can affect childreen
+ - + + - - -
  • Rash
  • Dyspnea
  • Weight loss
  • Cough
  • Heliotrope rash on face and hands
  • Telangectasia
  • Erythema
  • Mechanic's hands
  • Gottron's sign ( violaceous scaly eruption )
  • ↑↑
  • Perimysial mononuclear infiltrate
  • Muscle inflammation and damage
Polymyositis[2]
  • > 18 years
+ - + + - - - - -
  • ↑↑
  • Endomysial mononuclear infiltrate
  • Patchy necrosis
Inclusion body myositis[3]
  • 50s
+ +
  • ↑↑
Fibomyalgia
  • 40-50s

+

- - - - ++ -
  • Anxiety or depression features
  • Fatigue
  • Sleep disturbance
  • Numbness
  • Muscle spasms
  • History of depressive disorder
  • Tenderness in the soft tissue anatomical location
  • Normal
  • Normal
  • Normal
  • Normal
Polymyalgia Rheumatica[4]
  • 50s
+ - + + - - -
  • Weight loss
  • History of joints stiffness which is worse in the morning
  • Restricted shoulder motion
  • ↑ CRP
  • ↑ ESR
  • Normal
  • Normal
  • Normal
Chronic Pain Syndrome
Genetic
Becker muscular dystrophy <13yrs + - - - + - -
  • Milder form of Duchenne
  • ↑↑
    • Muscle fibril degeneration, regeneration
    • Isolated fiber hypertrophy
    • Muscle replacement with fat and connective tissue
  • Weakness is caused by destruction of muscle.
Duchenne muscular dystrophy <13 yrs + - - - + - -
  • Calf psedohypertrophy
  • Cardiomyopathy
  • Kyphoscoliosis
  • Cognitive impairment
  • +Grower sign
  • ↑↑
Limb-girdle muscular dystrophies <15 yrs + - - + + - -
  • Calf hypertrophy
  • Scapular winging
  • Cardiomyopathy
  • Cardiac arrhythmias
  • Respiratory muscle weakness
  • Autosomal dominant
  • LMNA gene
  • CAV3 gene
  • ↑↑
  • -
Myotonic dystrophy type 1 + + - - + - -
  • Myotonia
  • Cataracts
  • Diabetes mellitus
  • Frontal balding
  • Cardiac arrhythmias
  • Cholecystitis
  • Pregnancy
  • Eyelid ptosis
Infectious
Lyme disease Variable + - + + +/- + -
  • + Tick bite
  • Hiking/Tip
  • Clinical diagnosis
  • +Serology
  • -
  • -
  • -
Infulenza Variable - - + + + - +
  • Fever
  • Malaise
  • Rhinorrhea
  • Muscle pain worse with movement
  • Muscle weakness, tenderness, and swelling.
  • ↑↑ Liver enzymes
  • +PCR
  • ↑↑
  • -
  • -
Polio <5 yrs + - - - + + -
  • Isolation from pharyngealsecretions, CSF
  • +Serology
  • -
  • -
  • Neurological pattern
Syphilis Variable - - - - + + -
  • Chancre
  • Lymphadenopathy
  • Condylomata lata
  • Neuro syphilis
  • Cardiovascular syphilis
  • History of risk factors (MSM, unprotected sex, multiple sex partners)
  • Darkfield examinations
  • VDRL
  • RPR
  • FTA-ABS
  • -
  • -
  • -
Pyomyositis Variable +/- +/- + + - - -
  • Fever
  • Malaise
  • Psoas abscess
  • Immunocopmprimised
    • Muscles are painful, swollen, tender, and indurated.
    • Depending on the site of involvement, it may mimic appendicitis (psoas muscle), septic arthritis of the hip (iliacus muscle), or epidural abscess (piriformis muscle).
  • Leukocytosis
  • Elevated ESR
  • -
  • -
  • -
Neurologic
ALS
Stroke
GBS
Multiple Sclerosis
Neuro-muscular
Botulisim
Lambert-Eaton myaes
Myasthenia gravis
Paraneoplastic
Metabolic
Glycogen storage disease
Lipid storage disease
Mitochondrial
  1. Dalakas MC (1991). "Polymyositis, dermatomyositis and inclusion-body myositis". N Engl J Med. 325 (21): 1487–98. doi:10.1056/NEJM199111213252107. PMID 1658649.
  2. Dalakas MC (1991). "Polymyositis, dermatomyositis and inclusion-body myositis". N Engl J Med. 325 (21): 1487–98. doi:10.1056/NEJM199111213252107. PMID 1658649.
  3. Dalakas MC (1991). "Polymyositis, dermatomyositis and inclusion-body myositis". N Engl J Med. 325 (21): 1487–98. doi:10.1056/NEJM199111213252107. PMID 1658649.
  4. Myklebust G, Gran JT (1996). "A prospective study of 287 patients with polymyalgia rheumatica and temporal arteritis: clinical and laboratory manifestations at onset of disease and at the time of diagnosis". Br J Rheumatol. 35 (11): 1161–8. PMID 8948307.