systemic lupus erythmatosous Flashcards

1
Q

define SLE

A

SLE is an inflammatory autoimmune connective tissue disorde

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2
Q

pathophysiology of SLE (full)

A
  1. B and T cells that react against self-antigens are usually destroyed in the bone marrow
  2. In SLE, these cells survive due to a defect in central or peripheral tolerance.
  3. Increased defective clearance of apoptotic cells, combined with the production of autoantibodies leads to the formation of immune complexes.
  4. These immune complexes are deposited in tissues and trigger a complement cascade, leading to further inflammation.
  5. The persistent inflammation of organs can lead to damage (e.g. glomerulonephritis).
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3
Q

pathophysiology of SLE (shortened)

A

aNA and antiDsDNA antibodies attack soft tissue causing chronic inflammation and damage

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4
Q

what type of hypersensitivity is SLE

A

HYPERSENSISITIVTY TYPE 3 - antigen antibody complex deposition

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5
Q

who is at high risk of SLE

A
  • Asian, African, Caribbean, and Hispanic patients
  • middle-aged adults
  • women
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6
Q

risk factors for SLE

A
  • female
  • drugs
  • genetics (HLAB8/DR2/DR3)
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7
Q

signs and symptoms of SLE

A
  • Fatigue
  • Weight loss
  • Arthralgia (joint pain)
  • Non-erosive arthritis
  • Myalgia (muscle pain)
  • Fever
  • Lymphadenopathy
  • Splenomegaly
  • Shortness of breath
  • Pleuritic chest pain
  • Mouth ulcers
  • Hair loss
  • Raynaud’s phenomenon
  • Oedema (due to nephritis)
  • Malar/butterfly rash (across the nose and cheeks and worsened/triggered by sunlight)
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8
Q

what investigations do you do for SLE

A
  1. bloods
  2. urine dipstick/urinalysis
  3. serology
  4. renal biopsy
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9
Q

what do bloods for SLE show

A
  1. anaemia (normocytic)
  2. raised ESR, normal CRP
  3. decreased C3 &C4
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10
Q

what does urinalysis of SLE show

A
  • proteinuria (in lupus nephritis)
  • haematuria
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11
Q

what does serology for SLE show

A
  • ANA Ab’s (85% of patients)
  • Anti dsDNA Ab’s (50% of patients)
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12
Q

which antibodies are more useful for SLE diagnosis

A

anti-dsDNA are highly specific so if present, high indication of SLE

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13
Q

how to look for specific antibodies

A

An extractable nuclear antigen looks for specific antibodies to distinguish between specific tissue disorders

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14
Q

what is antiphospholipid syndrome

A

Antiphospholipid antibodies/syndrome can occur secondary to SLE in 40% of patients.

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15
Q

how to establish a diagnosis for SLE

A

Patients are diagnosed using the European League Against Rheumatism or American College of Rheumatology criteria.

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16
Q

first line treatment for SLE

A

Hydroxychloroquine, NSAIDS, and steroids

17
Q

treatment for more resitant forms of SLE

A

DMARDs and biological therapies (rituximab and belimumab)

18
Q

what is Discoid Lupus Erythematosus

A

affects the skin and is common in darker-skinned patients.
Lesions appear on the skin, and they are photosensitive.

19
Q

symptoms of discoid lupus erythematosus

A
  • Scarring alopecia
  • hyperpigmentation
  • hypopigmentation
20
Q

how to diagnose discoid lupus erythematosus

A

skin biopsy

21
Q

treatment of discoid lupus erythematosus

A
  • sun protection
  • steroids
  • hydroxychloroquine.
22
Q

does SLE cause illness/death

A

no illness/death are due to a complication of SLE

23
Q

complications of SLE

A
  • cardiovascular disease
  • infection
  • pericarditis
  • pleuritis
  • interstitial lung disease
  • lupus nephritis
  • neuropsychiatric SLE
  • recurrent miscarriage
  • venous thromboembolism