Myopathy
Myopathies are neuromuscular diseases affecting primarily skeletal muscles. They are usually symmetrical and mainly affect the limbs girdle but it can also be an oculopharyngeal or fascioscapular form.
The main clinical picture is proximal muscle weakness. We also observe myopathic "duck" walking due to weakened gluteal muscles. The patient does not keep the pelvis horizontal, does not stand up without help and we observe the so-called Gower sign - myopathic climbing. Other features are hyperlordosis, atrophy, hypotrophy (thigh muscles) or hypertrophy (rather pseudohypertrophy = muscle turns into ligament or fat replacement of muscle), decreased reflexes, no sensory hypoesthesia.
Etiology[edit | edit source]
The following diseases can be included among myopathies :
Genetically determined myopathies[edit | edit source]
- Duchenne muscular dystrophy
- Becker muscular dystrophy
Acquired myopathies[edit | edit source]
- inflammatory – polymyositis, dermatomyositis;
- endocrine/ metabolic conditioned – hypo/hyperthyroidism, Cushing, hypokalaemia
- toxic and drug-inducted myopathies – alcohol, corticoids, statins, antirheumatics/ anti-inflammatory/ immunosuppressants – colchicine, steroids, D-penicillamine, chloroquine
- myotonia – do not manifest as a typical myopathic syndrome, but hypertension dominates
The clinical picture[edit | edit source]
The clinical picture is dominated by muscle weakness. Muscle reflexes may be reduced but not extinguished. Muscle pain may or may not be present depending on the specific cause. Muscle involvement is usually symmetrical and (unlike neuropathies) mainly on the proximal girdle muscles. This gives rise to a typical myopathic syndrome which includes:
- myopathic ("duck") gait – while walking, the pelvis on the side of the foot drops, which is just taking a step (normally the pelvis on this side rises to relieve the foot)
- hyperlordosis of lumbar spine with protruding abdomen
- myopathic climbing – when getting up from a squat, the patient help each other with their hands
Patients typically have difficulty walking up the stairs and getting up from chair. When their upper limbs are affected, they have trouble hanging clothes and brushing their hair.
| Parameter | Myastenia | Myopathy |
|---|---|---|
| Name | astenia = weakness | patia = disorder |
| Disability | neuromuscular disc | muscle |
| Location | generalized | proximal limbs |
| Sensory impairment | no | no |
| Pain | no | yes |
| Atrophy | no | yes |
| Fasculation | no | no |
| Proprioceptive feeling | standard | standard or reduced |
| Tone | standard | reduced |
Diagnosis[edit | edit source]
- EMG – on conventional EMG we see the activation of a large number of motor units at a given load than in normal muscle
- serum muscle enzymes – increased CK and myoglobin
- muscle biopsy – atrophy, hypotrophy, pseudohypertrophy;
- dystrophin protein deficiency
- EKG, echo;
- spirometry – respiratory muscles
References[edit | edit source]
Related Articles[edit | edit source]
References[edit | edit source]
- AMBLER, Zdeněk. Základy neurologie : [učebnice pro lékařské fakulty]. 7. edition. Praha : Galén, c2011. ISBN 9788072627073.
- KÁBRT, Jan, et al. Lexicon medicum. 1. edition. 1988. ISBN 08-063-88.
