Textbook of Pediatric Rheumatology

Antiphospholipid Syndrome

Antiphospholipid syndrome (APS) is an autoimmune multisystem disease primarily manifested as intravascular thrombosis and mediated by antiphospholipid antibodies (APLA). APS may occur as an isolated clinical entity (primary APS) or in association with other autoimmune diseases (secondary APS), particularly systemic…

Uveitis in Juvenile Idiopathic Arthritis

Inflammatory eye diseases comprise some of the most devastating complications of childhood rheumatic diseases, especially juvenile idiopathic arthritis (JIA). Chronic (initially asymptomatic) uveitis accompanying JIA is one of the most common causes of uveitis in childhood. It is predominantly anterior,…

Psoriatic Juvenile Idiopathic Arthritis

The association of arthritis with psoriasis was described almost 200 years ago, but it was not reported in children until the 1950s. Psoriatic juvenile idiopathic arthritis (PsJIA) is a heterogeneous entity, recognized in patients with frank psoriasis but also where…

Enthesitis-Related Arthritis

Definition and Classification Under the International League of Associations for Rheumatology (ILAR) classification of juvenile idiopathic arthritis (JIA), , enthesitis-related arthritis (ERA) is defined according to the inclusion and exclusion criteria shown in Table 20.1 . Children with ERA have…

Polyarticular Juvenile Idiopathic Arthritis

Definitions Chronic childhood arthritis affecting five joints or more during the first 6 months of disease is defined as polyarthritis . , The International League of Associations for Rheumatology (ILAR) classification system for juvenile idiopathic arthritis (JIA) further categorizes polyarthritis…

Systemic Juvenile Idiopathic Arthritis

Systemic juvenile idiopathic arthritis (sJIA) is one of the most perplexing diseases of childhood. Its onset can be quite nonspecific and may suggest bacterial or viral infection, malignancy, or another inflammatory disease. The evolution of the disease eventually confirms the…