Arthritis Cure Poncet's disease is an aseptic inflammatory polyarthritis that occurs in the presence of TB disease. ... Most cases resolve after satisfactory treatment of the TB.
|Systemic-onset juvenile idiopathic arthritis|
|Other names||Systemic juvenile idiopathic arthritis|
Arthritis Curehow to Arthritis Cure for Systemic-onset juvenile idiopathic arthritis (or the juvenile onset form of Still''s disease.
Predominantly extra-articular manifestations like high fevers, rheumatic rash, enlargement of the liver and spleen, enlargement of the lymph nodes, and anemia. Others manifestations include inflammation of the pleura, inflammation of the pericardium, inflammation of the heart''s disease. However, there is some evidence that the two conditions are closely related.
Systemic JIA is characterized by arthritis, fever, which typically is higher than the low-grade fever associated with polyarticular and a salmon pink rash. It accounts for 10-20% of JIA and affects males and females equally, unlike the other two subtypes of JIA, and affects adolescents. It generally involves both large and small joints. Systemic JIA can be challenging to diagnose because the fever and rash come and go. Fever can occur at the same time every day or twice a day (often in late afternoon or evening) with a spontaneous rapid return to baseline (vs. septic arthritis of continuous fever). The rash often occurs with fever. It is a discrete, salmon-pink macules of different sizes. It migrates to different locations on skin, rarely persisting in one location more than one hour. The rash is commonly seen on trunk and proximal extremities or over pressure areas.
Arthritis is often absent in the first weeks or even 6–8 months into the illness.
Systemic JIA may have internal organ involvement such as hepatosplenomegaly, lymphadenopathy, serositis, hepatitis, or tenosynovitis.[citation for 1 last update 2020/08/05 neededcitation needed]
A polymorphism in macrophage migration for 1 last update 2020/08/05 inhibitory factor has been associated with this condition. A polymorphism in macrophage migration inhibitory factor has been associated with this condition.