Health knowledge: these diseases are also rheumatism

Osteoarthritis

Osteoarthritis is a degenerative disease, which is due to age, obesity, strain, trauma, congenital anomalies of the joints, joint deformities and other factors caused by degenerative articular cartilage damage, joint edge and subchondral bone reactive hyperplasia, also known as bone Arthropathy, degenerative arthritis, senile arthritis, hypertrophic arthritis, etc. The clinical manifestations are slowly developing joint pain, tenderness, stiffness, swollen joints, limited mobility, and deformed joints.

Ankylosing spondylitis

Many people think that ankylosing spondylitis is an orthopedic disease. In fact, it is a seronegative "rheumatism." The mechanism of pathogenicity is still not clear. Current research suggests that there is a close relationship with genetics. There are more male patients than female patients, and the majority are young males.

Many patients with ankylosing spondylitis have low back pain at the onset of illness and are characterized by stiffness in the morning and back, and decreased pain after activity. The development of ankylosing spondylitis eventually leads to deformity of the spine or hip joint. In the X-ray photograph, the "rigid" spine shows a bamboo-like change, the patient can not even take care of themselves, and even if the surgery is performed late, it cannot be completely improved. However, if the early detection and early intervention, the situation will be very different.

Lupus erythematosus

Lupus erythematosus (LE) is a typical autoimmune connective tissue disease that is more common in women aged 15 to 40 years. The etiology has not yet been fully understood and is currently believed to be related to heredity, sex hormones, and environmental factors. Lupus erythematosus is divided into many types, of which systemic lupus erythematosus is the most serious type. The vast majority of patients have multiple systemic lesions at the time of onset, and some patients are also accompanied by other connective tissue diseases such as scleroderma, dermatomyositis, and Sjogren's syndrome to form various overlapping syndromes. The clinical manifestations of systemic lupus erythematosus are diverse, complex, and often severe. Patients may be life-threatening due to lupus nephritis, lupus encephalopathy, and the long-term side effects of extensive use of drugs.

gout

Gout is a metabolic disease caused by increased uric acid production caused by abnormal purine metabolism. When acute gout occurs, urate crystals are deposited on the joints. The joints show severe pain, swelling, erythema, stiffness, and fever. The sudden onset of symptoms often involves the first metatarsophalangeal joint and causes acute inflammatory reactive slip. Membrane inflammation. Most patients are induced after minor trauma or eating purine-rich foods (especially drinking beer or eating seafood, eating hot pots) and drinking alcohol.

Behcet disease

Behcet's disease is a kind of vasculitis. Most patients only invade the submucosal small blood vessels and cause mucosal ulcers. However, a small number of Behcet's disease can affect the blood vessels of the whole body, causing major blood vessels or internal organs to be damaged and life-threatening. In general, the majority of female patients are mild, mainly mucosal ulcers; while the majority of male patients are heavier, often involving internal organs and blood vessels. If more than three times a year, oral ulcers, genital ulcers, eye and skin problems, joint pain, etc., need to be alert to Behcet's disease, it is recommended to the Department of Rheumatology and Immunology. Although current Behcet's disease is still an incurable disease, standardized anti-inflammatory and immunotherapy can often achieve the effect of relieving the disease.

Dermatomyositis

Dermatomyositis is also rheumatism. It is a non-suppurative inflammatory lesion mainly involving striated muscle, mainly lymphocytic infiltration, with or without multiple skin lesions, and may also be associated with various visceral lesions. The exact cause is not yet known. It may be a viral infection. Abnormal immune recognition of the body and self-identification and vascular lesions may also be related to each other. Any part of the muscle can be affected, but the proximal muscles of the limbs, the flexor of the neck, the paraspinal muscles, and the pharynx muscles are the most common. The onset of the disease is more insidious, and the disease is mostly developed in weeks or months to the peak. The average patient is 3 to 6 months from feeling unable to go to the hospital, and a few are acute or subacute.

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