Myopathy

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Myopathy
Specialty Rheumatology
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Myopathy is a disease of the muscle[1] in which the muscle fibers do not function properly. This results in muscular weakness. "Myopathy" simply means muscle disease (Greek myo- "muscle" + patheia < -pathy "suffering"). This meaning implies that the primary defect is within the muscle, as opposed to the nerves ("neuropathies" or "neurogenic" disorders) or elsewhere (e.g., the brain). Muscle cramps, stiffness, and spasm can also be associated with myopathy.

Muscular disease can be classified as neuromuscular or musculoskeletal in nature. Some conditions, such as myositis, can be considered both neuromuscular and musculoskeletal.

Signs and symptoms

Common symptoms include muscle weakness, cramps, stiffness, and tetany.

Systemic diseases

Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug- and toxin-induced, critical illness myopathy, metabolic, collagen related,[2] and myopathies with other systemic disorders. Patients with systemic myopathies often present acutely or sub acutely. On the other hand, familial myopathies or dystrophies generally present in a chronic fashion with exceptions of metabolic myopathies where symptoms on occasion can be precipitated acutely. Most of the inflammatory myopathies can have a chance association with malignant lesions; the incidence appears to be specifically increased only in patients with dermatomyositis.[3]

There are many types of myopathy. ICD-10 codes are provided here where available.

Inherited forms

Acquired

  • (G72.0 - G72.2) External substance induced myopathy
  • (M33.0-M33.1)
    • Dermatomyositis produces muscle weakness and skin changes. The skin rash is reddish and most commonly occurs on the face, especially around the eyes, and over the knuckles and elbows. Ragged nail folds with visible capillaries can be present. It can often be treated by drugs like corticosteroids or immunosuppressants. (M33.2)
    • Polymyositis produces muscle weaknesss. It can often be treated by drugs like corticosteroids or immunosuppressants.
    • Inclusion body myositis is a slowly progressive disease that produces weakness of hand grip and straightening of the knees. No effective treatment is known.
  • (M61) Myositis ossificans
  • (M62.89) Rhabdomyolysis and (R82.1) myoglobinurias

The Food and Drug Administration is recommending that physicians restrict prescribing high-dose Simvastatin (Zocor, Merck) to patients, given an increased risk of muscle damage. The FDA drug safety communication stated that physicians should limit using the 80-mg dose unless the patient has already been taking the drug for 12 months and there is no evidence of myopathy. "Simvastatin 80 mg should not be started in new patients, including patients already taking lower doses of the drug," the agency states.

Differential diagnosis

At DeathMlg '

None as systemic causes; mainly hereditary

Onset in childhood

Inflammatory myopathies – dermatomyositis, polymyositis (rarely)

Infectious myopathies

Endocrine and metabolic disorders – hypokalemia, hypocalcemia, hypercalcemia

Onset in adulthood[7]

Inflammatory myopathies – polymyositis, dermatomyositis, inclusion body myositis, viral (HIV)

Infectious myopathies

Endocrine myopathies – thyroid, parathyroid, adrenal, pituitary disorders

Toxic myopathies – alcohol, corticosteroids, narcotics, colchicines, chloroquine

Critical illness myopathy

Metabolic myopathies

Paraneoplastic myopathy

Treatments

Because different types of myopathies are caused by many different pathways, there is no single treatment for myopathy. Treatments range from treatment of the symptoms to very specific cause-targeting treatments. Drug therapy, physical therapy, bracing for support, surgery, and massage are all current treatments for a variety of myopathies.

References

  1. ^ "Myopathy - Definition from the Merriam-Webster Online Dictionary". 
  2. ^ Voermans NC1, van Alfen N, Pillen S, Lammens M, Schalkwijk J, Zwarts MJ, van Rooij IA, Hamel BC, van Engelen BG. (2009). "Neuromuscular involvement in various types of Ehlers-Danlos syndrome.". Ann Neurol. 65: 687–97. PMID 19557868. doi:10.1002/ana.21643. 
  3. ^ Chawla, Jasvinder (2011). "Stepwise Approach to Myopathy in Systemic Disease". Frontiers in Neurology. Front Neurol. 2011; 2: 49. 2: 49. PMC 3153853Freely accessible. PMID 21886637. doi:10.3389/fneur.2011.00049. 
  4. ^ Seene T (July 1994). "Turnover of skeletal muscle contractile proteins in glucocorticoid myopathy". J. Steroid Biochem. Mol. Biol. 50 (1–2): 1–4. PMID 8049126. doi:10.1016/0960-0760(94)90165-1. 
  5. ^ "Information On Sycamore Poisoning". Rainbow Equine Hospital. Retrieved 16 May 2017. 
  6. ^ "Equine Atypical Myopathy toxin and biochemical tests and tree sample testing available at the RVC". Royal Veterinary college - University of London. 13 February 2017. Retrieved 16 May 2017. 
  7. ^ Chawla, Myopathy (2011). "Systemic Myopathy". Frontiers in Neurology. 2: 49. PMC 3153853Freely accessible. PMID 21886637. doi:10.3389/fneur.2011.00049. 

External links

Classification
V · T · D
External resources


  • GeneReviews/NCBI/NIH/UW entry on Myopathy with Deficiency of ISCU
  • See http://neuromuscular.wustl.edu/ for medical descriptions.
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