Systemic sclerosis is a chronic autoimmune connective tissue disease characterised by skin fibrosis (scleroderma), fibrosis of the internal organs, vasculopathy, and immune system dysregulation. It is more common in women and peaks between 60 and 70 years. Classification Classification Description…
Sjögren’s syndrome is a chronic autoimmune disorder characterized by lymphocytic infiltration and fibrosis of exocrine glands; it primarily affects the salivary and lacrimal glands. It affects women more than men (M: F 9:1) and peaks between 40 and 60 years. It is…
Bechet’s syndrome is a chronic multisystemic inflammatory disorder characterised by recurrent oral and genital ulcers, uveitis, and skin lesions. It is associated with HLA-B5. The diagnosis is clinical. It is more prevalent in countries along the Silk Road, from Eastern…
Vasculitides are autoimmune inflammatory disorders of blood vessels that can affect any organ. They can be primary or secondary to other conditions, e.g., SLE, rheumatoid arthritis, hepatitis B and C, and HIV. Symptoms depend on the organ affected. The classification…
Fibromyalgia is a syndrome characterised by widespread pain throughout the body with tender points at specific anatomical sites. The diagnosis is likely if a patient is tender in at least 11 of 18 tender points. It accounts for 10% of…
Pseudogout is caused by the deposition of calcium pyrophosphate dihydrate crystals in the synovium. Clinical features of pseudogout Clinical feature Description Acute CPPD crystal arthritis Acute monoarthropathy affecting large joints in the elderly. Chronic CPPD Symmetrical polyarthritis and synovitis (like…
Gout is an acute-onset, crystal-induced arthritis that is characterised by intense joint pain and swelling – typically in the first metatarsal-phalangeal joint – when monosodium urate crystals are deposited. Definition of terms Term Definition Asymptomatic hyperuricaemia Elevated serum urate level…
Antiphospholipid syndrome is an autoimmune condition that is characterised by CLOTs: coagulation defects (arterial/venous), livedo reticularis, obstetric complications (recurrent miscarriage), and thrombocytopaenia (due to a thrombotic tendency). Antiphospholipid antibodies cause it.
Systemic Lupus Erythematosus (SLE) is a chronic, autoimmune, multi-systemic syndrome. It presents with the classic triad of fever, arthralgia and rash (malar, discoid or photosensitive). Black, Hispanic, and Asian people are affected at higher rates than white people. Women of…
Mixed connective tissue disease combines clinical features of systemic sclerosis, SLE, and polymyositis. It is associated with high titres of anti-U1-RNP antibodies. It is more common in women and peaks between 30 and 40 years of age. Systemic features System…