Histo: Connective tissue disease, amyloid, sarcoid, Immune related multisystem disorders Flashcards

1
Q

Give an example of an autoimmune disease that is:

  1. Organ-specific with a specific antigen
  2. Organ-specific without a specific antigen
  3. Multisystem disease
A
  1. Organ-specific with a specific antigen: pernicious anaemia
  2. Organ-specific without a specific antigen: primary biliary cirrhosis
  3. Multisystem disease: rheumatoid arthritis, Sjogren syndrome, SLE
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2
Q

What are the main features of SLE?

A

SOAP

  • Serositis
  • Oral ulcers
  • ANA
  • Photosensitivity

Brain

  • Bloods (low counts)
  • Renal (proteinuria)
  • Arthritis
  • Immunological (anti-dsDNA)
  • Neurological (psychiatric, seizures)

MD

  • Malar rash
  • Discoid rash

SOAP BRAIN MD

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3
Q

What units are used for ANA levels?

A

It is a titre - the highest dilution at which you can see the fluorescence (e.g. 1:1000 is a higher level than 1:10)

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4
Q

List three autoantibodies found in SLE. Which is most specific?

A
  • Anti-dsDNA
  • Anti-Smith (Sm, against ribonucleoproteins) - most specific but low sensitivity
  • Anti-histone - drug-related (e.g. hydralazine)
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5
Q

How is anti-dsDNA measured?

A

ELISA

Crithidia luciliae

  • Incubate the patient’s serum with Crithidia Luciliae (protozoan)
  • It has a big organism with dsDNA (kinetoplast) so if the patient has anti-dsDNA antibodies it will bind to the dsDNA in the kinetoplast
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6
Q

What can be seen on blood film in SLE?

A

LE (lupus erythromatosus) cell - neutrophil or macrocyte that has engulfed nuclear material of another cell

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7
Q

Describe the appearance of skin histology in SLE.
What would immunofluorescence show?

A
  • Lymphocytic infiltration of the dermis
  • Vacuolisation (dissolution of the cells) of the basal epidermis
  • Extravasation of blood causes a rash

NOTE: immunofluorescence will show immune complex deposition at the epidermis-dermis junction

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8
Q

Describe the appearance of renal histology in SLE.

A

Thickened pink glomerular capillaries (wire-loop capillaries) due to immune complex deposition.

NOTE: immune complex deposition can be visualised by immunofluorescence

This is what a normal glomerulus looks like

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9
Q

What is the name of non-infective endocarditis associated with SLE?

A

Libman-Sacks endocarditis

NOTE: the vegetation is made up of fibrin, lymphocytes, neutrophils, histocytes

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10
Q

What is scleroderma?

A

An autoimmune condition characterised by excess collagen deposition and fibrosis

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11
Q

What is the localised skin-only form of scleroderma called?

A

Morphoea (sclerosis of skin only)

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12
Q

What are the two types of scleroderma?
Name the antibodies that they are associated with.

A

Diffuse

  • Involves the trunk and proximal limbs
  • Anti-Scl70 antibodies (anti-topoisomerase)

Limited (CREST syndrome)

  • Only affects skin distal to the elbows and knees
  • Anti-centromere antibodies
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13
Q

What are the main features of limited cutaneous systemic sclerosis (CREST syndrome)?

A
  • Calcinosis
  • Raynaud’s phenomenon
  • Esophageal dysmotility
  • Sclerodactyly
  • Telangiectasia
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14
Q

What pattern of ANA immunofluorescence is seen in scleroderma?

A

Nucleolar

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15
Q

Describe the skin histology in scleroderma.

A

Increased depth and amount of collagen (results in reduced skin elasticity)

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16
Q

How does scleroderma cause gastric and oesophageal dysmotility?

A

Collagen deposition (fibrosis) with the submucosa - affects muscle contraction

17
Q

Describe the vascular histology in scleroderma.

A

Intimal proliferation gives an onion skin appearance.

18
Q

What is a major consequence of vascular damage in scleroderma?

A

Renal hypertensive crisis

19
Q

What is mixed connective tissue disease?

A

A condition characterised by the overlap of several connective tissue diseases including SLE, scleroderma, polymyositis and dermatomyositis

20
Q

What ANA immunofluorescence pattern is seen in mixed connective tissue disease?

21
Q

What is dermatomyositis?

A

A condition characterised by proximal muscle pain and weakness and skin changes

22
Q

Which marker would be raised in the blood in dermatomyositis?

A

Creatine kinase

23
Q

What signs would be seen on the skin in dermatomyositis?

A
  • Gottren’s papules
  • Heliotrope rash
  • Facial rash
  • Systemic v-shaped rash
24
Q

What is sarcoidosis of the skin called?

A

Lupus pernio

25
List some features of sarcoidosis.
26
What is the pathological hallmark of sarcoidosis?
Non-caseating granuloma | Langhans giant cell, epitheloid macrophages, lymphocytes
27
What are some biochemical changes seen the blood in sarcoidosis?
* Hypergammaglobulinaemia * Raised ACE * Hypercalcaemia (due to 1-alpha hydroxylase expression by granuloma macrophages)
28
What criteria is used to classify vasculitides based on the size of the vessel?
Chapel Hill Criteria
29
What is polyarteritis nodosa? What are its main features?
* A necrotising arteritis which is focal and sharply demarcated * It heals by fibrosis and mainly affects the **renal** and **mesenteric** vessels * May present with gut ischaemia or renal impairment * It produces a rosary beads (nodular) appearance on angiography due to multiple aneurysms
30
Which infection is polyarteritis nodosa associated with?
Hepatitis B
31
What is a characteristic feature of vasculitis?
Palpable purpuric rash
32
How is temporal arteritis diagnosed and treated?
Diagnosis - Clinical - High ESR - Temporal artery biospy Treatment * High dose prednisolone
33
What will be seen on temporal artery biopsy in temporal arteritis?
Lymphocytic infiltration of the tunica media
34
What is Kawasaki disease? What are the main clinical features?
Medium vessel vasculitis Fever lasting longer that 5 days accompanied by: * Conjunctivitis * Rash * Adenopathy * Strawberry tongue * Hand and feet skin desquamation
35
What is a complication of Kawasaki's?
Coronary artery aneurysm (screen using echocardiogram)
36
What are the main features of granulomatosis with polyangiitis (Wegner's)?
* **ENT** - nosebleeds, sinusitis, saddle nose * **Lungs** - haemoptysis, SoB * **Kidneys** - haematuria
37
Which antibody is associated with granulomatosis with polyangiitis?
cANCA - directed against proteinase 3
38
What are the main features of eosinophilic granulomatosis with polyangitis (Churg-Strauss)?
* Asthma (1st stage) * Eosinophilia (2nd stage) * Vasculitis (3rd stage)
39
Which antibody is associated with Churg-Strauss syndrome?
pANCA - directed against myeloperoxidase