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729.0 Rheumatism unspecified and fibrositis; 729.1 Myalgia and myositis, Fibromyositis; 729.2 Neuralgia neuritis and radiculitis unspecified; 729.3 Panniculitis unspecified; 729.4 Fasciitis unspecified; 729.5 Pain in limb; 729.6 Foreign body in soft tissue; 729.7 Nontraumatic compartment syndrome
The infection can affect any skeletal muscle, but most often infects the large muscle groups such as the quadriceps or gluteal muscles. [2] [4] [5] Pyomyositis is mainly a disease of children and was first described by Scriba in 1885. Most patients are aged 2 to 5 years, but infection may occur in any age group.
Injury - A mild form of myositis can occur with hard exercise. [4] A more severe form of muscle injury, called rhabdomyolysis, is also associated with myositis. [4] This is a condition where an injury to the patient's muscles causes them to quickly break down. [4] Medicines - A variety of different medicines can cause myositis.
(G71.0) Dystrophies (or muscular dystrophies) are a subgroup of myopathies characterized by muscle degeneration and regeneration. Clinically, muscular dystrophies are typically progressive, because the muscles' ability to regenerate is eventually lost, leading to progressive weakness, often leading to use of a wheelchair, and eventually death, usually related to respiratory weakness.
It can also be associated with underlying cancer. The main classes of idiopathic inflammatory myopathy are polymyositis (PM), dermatomyositis (DM) (including juvenile, amyopathic, and sine-dermatitis form), inclusion-body myositis (IBM), immune-mediated necrotising myopathy (IMNM), and focal autoimmune myositis. [1]
This is a shortened version of the twelfth chapter of the ICD-9: Diseases of the Skin and Subcutaneous Tissue.It covers ICD codes 680 to 709.The full chapter can be found on pages 379 to 393 of Volume 1, which contains all (sub)categories of the ICD-9.
Myositis ossificans comprises two syndromes characterized by heterotopic ossification (calcification) of muscle. In 2020, the World Health Organization classified myositis ossificans together with fibro-osseous pseudotumor of digits as a single specific entity in the category of fibroblastic and myofibroblastic tumors .
953.9 Injury to unspecified site of nerve roots and spinal plexus; 954 Injury to other nerve(s) of trunk, excluding shoulder and pelvic girdles; 955 Injury to nerve(s) of shoulder girdle and upper limb. 955.0 Injury to axillary nerve; 955.1 Injury to median nerve; 955.2 Injury to ulnar nerve; 955.3 Injury to radial nerve; 955.4 Injury to ...