Connective tissue Flashcards

1
Q

features of SLE

A

SOAP BRAIN MD

Serositis 
Oral ulcers 
Arthritis 
photosensitivity 
Blood (all counts low) 
Renal (proteinuria) 
ANA 
Immunologic (anti-dsDNA) 
Neuro (psych, seizures)
Malar rash 
Discoid rash
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2
Q

What does ANA show

A

shows that the patient has antibodies that bind to nuclear antigen

Non specific

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3
Q

What are antibodies in SLE

A

anti-dsDNA
anti-smith
anti-histone

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4
Q

What is the most specific antibody for SLE

A

anti-smith

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5
Q

how do you measure anti dsDNA

A

incubate patients serum with Crithidia Luciliae (has big mitochondrion with double stranded DNA)
anti-dsDNA will bind to this

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6
Q

What does skin histology in SLE look like

A

Lynmphocytc infiltration of dermis
Vacuolisation
Extravasation or RBC - causes rash

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7
Q

what are glomerular capillaries in SLE like

A

WIRE LOOP capillaries (thickened)

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8
Q

what is the endocarditis in SLE

A

Libman Sacks

NON INFECTRIVE

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9
Q

how does Libman sacks present

A

emboli, heart failure, murmurs

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10
Q

What are the features of limited scleroderma

A

CREST

Calcinosis 
Raynauds 
Eosphageal dysmotolity 
Sclerodactyly 
Telangectasia
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11
Q

What is raynauds phenomenon in limited scleroderma

A

white > blue > red

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12
Q

what antibodies are linked to the diffuse scleroderma

A

DNA topoisomerase

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13
Q

What is the difference between limited and diffuse scleroderma

A

diffuse involves the trunk

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14
Q

what is the vascular histology of SLE

A

intimal proliferation, gives onion skin appearance

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15
Q

what is the appearance of ANA on immunofluorescence

A

speckled

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16
Q

what papule are indicative of dermatomyositis

A

Gottron’s papules (erythematous rash over knuckles)

17
Q

What are skin features of sarcoidosis

A

Skin - lupus pernio, erythema nodosum

18
Q

what is the hallmark of sarcoidosis

A

non-caseating granulomatous inflammation

19
Q

what criteria are used for classifying vasculitis based on vessel size

A

Chapel Hill Criteria

20
Q

what is polyarteritis nodosa

A

Necrotising artritis

Infiltration by polymorphs, lymphocytes, eosinophils > heals bu fibrosis

21
Q

What is the appearance on angiogram of polyarteritis nodos

A

Rosary beads appearance

due to the presence of multiple aneurisms

22
Q

What virus is polyarteritis nodosa associated ewith

A

Hep B

23
Q

Ix for temporal arteritis

A

ESR

Temporal artery biopsy

24
Q

Tx for temporal arteritis

A

high done prednisolone

25
Q

Three hallmarks for WegeneRRRs Granulomatosis (with polyangitis)=

A

RHINO - nosebleeds, sinusitis, saddle nose
RESP - haemoptysis, SOB
RENAL - haematuria

26
Q

antibody of Wegeners Granulomatosis (with polyangitis)=

A

c-ANCA

27
Q

Hallmarks of Churg Strauss Syndrome

A

Eva Churg Strauss

Eosinophilia
Vasculitis
Asthma

28
Q

what its antibody in Churg Strauss Syndrome

A

pANCA

29
Q

what is pANCA directed against

A

myeloperoxifdase

30
Q

what is cANCA directed against

A

Proteinase 3

31
Q

What does NON caseating granuloma mean

A

A granuloma that is not necrotic

32
Q

describe shared. fts of dermatomyositis and poliomyositis

A

proximal muscle fatigue (hips, shoulders) Thoracic muscle (lungs dyspnoea, heart arrhyth, oesophagus (dysmotility)-

ocular muscle spared

33
Q

what are fts of dermatomyositis only

A

Gottron papuls

Heliotropic rash