Study Notes on Rheumatology

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21 Terms

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Rheumatism or rheumatic disorders
Conditions causing chronic, often intermittent pain affecting the joints or connective tissue, encompassing at least 200 different conditions, including arthritis.
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Raynaud's Phenomenon
A health condition in which the blood vessels in an individual's body narrow in response to cold and stress, leading to transient malperfusion of fingers, toes, nose, and ears.
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Sequence of color change in Raynaud's Phenomenon
Initially white (lack of blood supply), then blue (absence of oxygen), and finally red (blood supply returns to normal).
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Rheumatoid Arthritis (RA)
An autoimmune disease that causes chronic inflammation of the joints and can also affect other organs, referred to as a systemic illness.
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Key symptom of RA stiffness
Most notable in the mornings and after inactivity.
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Typical deformities in late-stage RA
"Boutonniere" deformity of the thumb and "Swan-neck" deformity of fingers, along with radial deviation of the hand and ulnar deviation of fingers.
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Rheumatoid factor
IgM autoantibodies against IgG, positive in 70% of RA patients, used for prognostic rather than diagnostic purposes.
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First-line drugs for RA
Aspirin and corticosteroids, used to reduce pain and inflammation.
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DMARDs (Disease-Modifying Antirheumatic Drugs)
Second-line drugs like gold, methotrexate, hydroxychloroquine that promote disease remission and prevent joint destruction but are not anti-inflammatory.
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Systemic Lupus Erythematosus (SLE)
An autoimmune disease characterized by periods of flares and remission, affecting various organs.
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Characteristic rash of SLE
Butterfly-shaped (malar) rash across the nose and cheeks.
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SLICC Classification Criteria for SLE
Require at least 4 criteria (1 clinical, 1 laboratory) OR biopsy-proven lupus nephritis with positive ANA or Anti-DNA.
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Scleroderma / Systemic Sclerosis
A condition progressing from localized to systemic, characterized by collagen accumulation causing organ infarctions and rigidity.
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CREST Syndrome
A limited form of scleroderma symptoms including Calci-Des deposits in skin, Raynaud’s phenomenon, Esophageal dysfunction, Sclerodactyly, and Telangiectasias.
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Anti-centromere antibodies
Antibodies identified in 70% of patients with limited cutaneous scleroderma.
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Dermatomyositis / Polymyositis
Conditions affecting proximal muscles, characterized by muscle weakness, pain, and fever, sometimes associated with malignancies.
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Sjögren’s Syndrome
A chronic disorder leading to insufficient moisture production in certain glands, causing dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia).
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Vasculitis
An inflammatory vascular disease instigated by immunological reactions, impacting various organs.
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Wegener Granulomatosis
A specific type of vasculitis characterized by granulomas, often starting in the upper respiratory tract before affecting systemic areas (pulmorenal syndrome).
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Granuloma
A structure formed during inflammation, a collection of immune cells (macrophages), formed by the immune system to wall off substances perceived as foreign.
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Giant Cell Arteritis
Common vasculitis in older women, presenting mainly as temporal arteritis, with symptoms like throbbing headaches in temples, eye pain, and a palpable painful hardened temporal artery.