Multisystem Autoimmune Diseases Flashcards

1
Q

What is Systemic Lupus Erythematous?

A

A chronic multi-system disorder that most commonly affects women during their reproductive years. It is characterised by the presence of antinuclear antibodies. In addition to constitutional symptoms, it most frequently involves the skin and joints, although serositis, nephritis, haematological cytopenias and neurological manifestations may occur during the course of the disease.

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2
Q

What are the risks factors for SLE?

A
Smoking
Female
Onset is 15-50 years old
Ethnicity- Afro-Caribbean and Asians more likely to be affected
FH
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3
Q

What are the cutaneous symptoms of SLE?

A
Butterfly rash on face that spares the nasal folds and is photosensitive
Discoid Rash
Urticaria
Vasculitis
Purpura
Oral Ulcers
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4
Q

What is seen on a blood test in SLE?

A

Thrombocytopenia
Anaemia
Leukopenia

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5
Q

What are the cardiac and respiratory symptoms involved in SLE?

A
Pericarditis
Endocarditis
Aortic Valve Lesions
Pleurisy
Fibrosis of the lungs
Pleural Effusion
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6
Q

What are the Neuro symptoms involved in SLE?

A
Seizures
Peripheral Neuropathy
Ataxia
Hemiplegia
Cranial Nerve Lesions
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7
Q

What other systems are affected by SLE?

A
Myopathy
Reynaud's phenomenon
Malaise
Depression
Abdominal Pain
Alopecia
Arthritis
Kidneys can shut down so need urine dipstick-symptoms of nephrosis
Dysphagia
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8
Q

What investigations should be done in SLE?

A
Do investigations specific to the symptoms of the system affected ie chest X rays for lungs etc
FBC
PTT
Us and Es
ESR
CRP
ECG
Complement Consumption in a complement test
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9
Q

What antibodies are found and should be tested for in SLE?

A

Smith Antigen
Anti Nuclear Antibodies
Double stranded antibodies

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10
Q

What is the management for SLE?

A

Manage the systemic symptoms appropriately

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11
Q

What is Scleroderma?

A

Systemic sclerosis (SSc), also known as scleroderma, is a multi-system, autoimmune disease, characterised by functional and structural abnormalities of small blood vessels, fibrosis of skin and internal organs, and production of auto-antibodies.

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12
Q

What are the risk factors for scleroderma?

A

FH
Exposure to toxins such as silica dust
Male
Onset is age 30-50 years old

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13
Q

What does CREST mean in scleroderma?

A
Calcified lesions on fingers
Reynaud's phenomenon
Oesophageal dysmotility
Sclerodactyly
Telangiectasia
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14
Q

What are the two types of scleroderma?

A

Limited

Diffuse

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15
Q

What are some complications of scleroderma?

A

Limited- Pulmonary hypertension
Diffuse-Pulmonary fibrosis
Renal crisis
Small bowel bacterial overgrowth

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16
Q

What antibodies are positive in scleroderma?

A

Auto antibodies- ANA antibodies

17
Q

What is Sjogren’s syndrome?

A

Sjogren syndrome is a systemic auto-immune disorder characterised by the presence of dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia) as a consequence of lymphocytic infiltration into the lacrimal and salivary glands.

18
Q

What are the risk factors for Sjogren’s syndrome?

A

Female
Peak ages at 20s to 30s and after the menopause
Genetic factors
Other autoimmune diseases (then called secondary Sjogren’s)
HLA markers

19
Q

What are the symptoms of Sjogren’s syndrome?

A
Dry eyes
Dry mouth
Fatigue
Vasculitis
Dental Caries
Increased oral infections due to less saliva
Arthralgia
Myalgia
Enlarged parotid glands
Facial pain
Kidney Disease
GI and CNS symptoms
Reynaud's phenomenon
Systemic Symptoms
20
Q

What investigations should be done for Sjogren’s syndrome?

A
Schirmer's test-quantitively measure tears
Anti-60KD and anti-LA antibodies
Parotid gland studies
Skin biopsy
Sialometry
21
Q

What are the symptoms of autoimmune myositis?

A

Proximal and symmetrical muscle weakness