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

23
Q

Ix for temporal arteritis

A

ESR

Temporal artery biopsy

24
Q

Tx for temporal arteritis

A

high done prednisolone

25
Three hallmarks for WegeneRRRs Granulomatosis (with polyangitis)=
RHINO - nosebleeds, sinusitis, saddle nose RESP - haemoptysis, SOB RENAL - haematuria
26
antibody of Wegeners Granulomatosis (with polyangitis)=
c-ANCA
27
Hallmarks of Churg Strauss Syndrome
Eva Churg Strauss Eosinophilia Vasculitis Asthma
28
what its antibody in Churg Strauss Syndrome
pANCA
29
what is pANCA directed against
myeloperoxifdase
30
what is cANCA directed against
Proteinase 3
31
What does NON caseating granuloma mean
A granuloma that is not necrotic
32
describe shared. fts of dermatomyositis and poliomyositis
proximal muscle fatigue (hips, shoulders) Thoracic muscle (lungs dyspnoea, heart arrhyth, oesophagus (dysmotility)- ocular muscle spared
33
what are fts of dermatomyositis only
Gottron papuls | Heliotropic rash