histo rheum Flashcards

(43 cards)

1
Q

histological findings for sarcoid

A

non caseating granulomas asteroid bodies Schaumann bodies

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2
Q

investigations for Sarcoid

A

raised Ca Raised ESR raised ACE Kveim test historically- intradermal injection of splenic sarcoid tissue and resultant granuloma formation

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3
Q

extra pulomary symptoms for sarcoid

A

weight loss night sweats hypercalcaemia/ hypercalciuria arthritis bone cysts erythema nodosum lupus pernio skin nodules ant/ post uveitis uveoparotid fever

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4
Q

what is uveoparotid fever

A

Heerfordt syndrome facial palsy bilateral uveitis parotid enlargment

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5
Q

amyloidosis

A

multisystem disease where misfolded proteins are deposited as fibrils in healthy tissue

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6
Q

primary amyloidosis protein

A

amyloid L

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7
Q

secondary amyloidosis protein

A

amyloid A

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8
Q

secondary amyloidosis associations

A

RA, ank spond TB renal cell carcinoma hodgkin lymphoma

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9
Q

familial amyloidosis alternative name

A

familial mediterranean fever

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10
Q

defect in familial mediterranean fever

A

pyrin gene overproduction of IL1

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11
Q

protein in haemodialysis associated amyloidosis

A

beta 2 microglobulin

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12
Q

diagnosis of amyloidosis

A

apple green bifringence under polarised light witha congo red stain

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13
Q

what causes the findings under polarised light in amyloidosis

A

beta sheets and the fibrils self assort as they are unstable

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14
Q

symptoms of amyloidosis

A

nephotic syndrome cardiac arrythmia carpal tunnel hepatosplenomegaly macroglossia in 10%

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15
Q

what are the large vessel vasculitides

A

temporal arteritis takayasu’s arteritis

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16
Q

who gets takayasu’s arteritis

A

middle aged japenese women

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17
Q

sx of takayasu’s arteritis

A

bruits pulseless disease claudications

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18
Q

temporal arteritis symptoms

A

jaw claudication scalp tenderness raised ESR

19
Q

histology of temporal arteritis

A

granulomatous transmural inflammation

20
Q

WHAT IS SEEN ON ANGIOPATHY OF POLYARTERITIS NODOSA

A

MICROANEURYSMS

21
Q

what disease predisposes you to PAN

23
Q

SLE reaction type

A

type 3 hypersesitivity

24
Q

autoantibodies in SLE

A

anti dsDNA antism anti histone ANA

25
hisotlogy of SLE
lupus erythematosus cell onion skin lesion in splenn libman sacks endocarditis microangiopathy in CNS
26
symptoms of SLE 4 of SOAP BRAIN MD
serositis Oral ulcers Arthritis Photosensitivity Blood disorders e.g. AIHA,lecopenia, ITP Renal involvment ANA +ve Immune pheonomena e..g antidsDNA ab Neuro sx malar rash discoid rash
27
HLA association ion SLE
HLA DR3 (or2)
28
HLA association for limited or diffuse scleroderma
HLA DR5 and DRw8
29
autoantibodie in limited scleroderma
anti centromere
30
sx oflimited scleroderma
calcinosis raynauds oesophageal dysmotility Sclerodactyly telangectasia pulm HTN
31
histology of limited scleroderma
onion skinning of arteries increased collagen in skin and organs
32
autoantibodies in diffuse scleroderma
anti scl-70 fibrillarin RNA polyermase I, II, III PM-Scl
33
histology of diffuse scleroserma
inflammation within and around muscle fibres
34
sx of diffuse scleroderma
skin and organ changes pulmonary fibrosis
35
dermatomyositis and polymyositis autoantibody
anit-Jo1
36
whatis anti Jo1
tRNA synthase
37
polymyositis histology
endomysial inflammatoary infiltrate
38
dermatomyositis histology
capilliary and myofibre damage
39
sx of dermatomyositis and polymyositis
proximal muscle weakness abnormal EMG raised CK
40
dermatomyositis cutaneous features
gotten papules on hands heliotrope rash on eyes
41
what is associated with dermatomyositis and polymyositis
underlying malignancy
42
what condition is associated with dermatomyositis
pulmonary fibrosis
43
difference between pemphigus and pemphigoid
pemphigoid forms subepidermal bullae and pehmigus forms intraepidermal IgG is linier in pemphigoid and netlike in pemphigus in pemphigoid the IgG binds to intercellular hemi desmosomes onBM whereas in pemphigus the IgG binds to demosomal proeteins