non neoplastic pathology Flashcards

(44 cards)

1
Q

histology of all CT disease =

diagnose by ___

A

chronic inflam with lots of plasma cells

autoIgs as commonly they are immune driven

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

secondary vasculitis is caused by ___

A

vessels are proximal to source of inflammation and it spreads to the vessels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

direct invasion and inflammation of the vessel walls can be caused by __

A

infection eg syphilis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

specific autoIg for Kawasaki’s disease

A

anti endothelial

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

cANCA: c stands for ___ and reacts with __

A

cytoplasmic

PR3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

pANCA: p stands for ___ and reacts with __

A

perinuclear

MPO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

large vessel vasculitis = _____ disease

eg.s (2)

A

granulomatous disease
GCA
Takayasu arteritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

medium vessel vasculitis = ___ eg. __

or ___ eg. ___

A

immune complex mediated eg. polyarteritis nodosa

anti-endothelial cell Igs eg. Kawasakis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

small vessel vasculitis with paucity of immune complexes (3 types)

A

vasculitis wo granuloma/asthma = microscopic polyangitis
granulomas no asthma = GPA
eosinophilia, asthma, granulomas = EPGA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

features = temporal arteritis which is __ and so -ve biopsy doesnt rule out
condition =

A

segmental

GPA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

give ___ prior to temporal artery biopsy in GPA

A

steroids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
polyarteritis nodosa (PAN) is a vasculitis of \_\_ vessels and is ANCA \_\_\_
presumed due to \_\_ as 1/3 are +ve for these
A

medium
-ve
circulating hep B immune complexes and Ig

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

polyarteritis nodosa spares __ and has a propensity for __+__ involvement
features of vessels involved = __+__

A

spares lungs
renal and GI
transmural necrotising inflam + fibrinoid necrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

immune complex mediated small vessel vasculitis eg.s (4)

A

SLE vasculitis
Henoch-Schonlein purpura (IgA)
Cryoglobulin vasculitis
Goodpasture’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

uric acid is end product of __

A

purine (A+G) degradation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

causes of gout that are caused by too much uric acid being produced

A
90% idiopathic with unknown enzyme defect
HGPRT defect ( rare = Lysch-Nyhan syndrome)
increased cell turnover - malig, psoriasis, chemo
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

causes of gout due to excrete too little uric acid =

A

thiazides

renal impairment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

uric acid crystals deposit in __ and ___ in gout

A

joints in lower temp

kidney tubules and interstitium (can also cause renal stones)

19
Q

uric acid crystal appearance on microscopy of fresh specimen

A

needle shaped and negative bifringence

20
Q

-ve bifringence means the orientation of the crystals =

21
Q

apple green bifringence with congo red staining =

A

amyloid protein

22
Q

pseudogout aka

caused by ___ crystals

A

chondrocalcinosis

calcium pyrophosphatase

23
Q

rhomboid shaped and weakly +ve bifrengence crystals =

A

calcium pyrophosphate

24
Q

increased osteoclast activity causing increased osteoblast activity is the underlying problem in

25
genetic elements of Pagets =
SQSTM1/p62 | RANKL - osteoclast receptor activator
26
Pagets can be caused be a ___ infection eg (3) or idiopathic
viral - paromyxovirus, measles ( nucleocapsid protein MVNP seems to stim osteoclasts) + RSV
27
3 stages of Pagets = __>__>__
osteolytic > mixed > burnt out
28
leontiasis ossea = | seen in __
overgrowth of facial and cranial bones seen in Pagets | also fibrous dysplasia, hyperparathyroidism and renal osteodystrophy
29
platybasia = | seen in __
abnormal flattening of the skull base | Pagets
30
sabre tibia is seen in what condition
Pagets
31
Pagets causes __ metabolism = __ skin, ____ HF | and increases ___ risk
increased - warm skin, high volume HF | osteosarcoma
32
rickety rosary = | sign seen =
2 lines in ribs with the abnormal one at the costochondral junction Rickets
33
bowed legs, square head, pigeon chest and rickety rosary are signs in
Rickets
34
#>____ (fibrin mesh)> ___ cell influx > ___ release > ___ cells from periosteum and medulla > __ (1wk) = ___ and remodelling at bone ends > 2-3 wk reach ___ -woven bone deposited ___ to cortical bone, some __ deposited which undergoes ___, bridging with ___ > remodelled
``` hamartoma inflammatory cell cytokine osteoprogenitor callus = organised hamartoma cartilage - endochondral ossification bony callus ```
35
kidney lung and breast mets to bone are usually osteo___
osteolytic
36
osteoclerotic metastasis =
prostate
37
creeping substitution on histology is a feature of
AVN
38
AVN is usually a ___ infarct and often __
wedge-shaped infarct | subcortical
39
bony lesions caused by proliferation of plasma cells
myeloma/plasmacytoma
40
polished bone in OA other name =
eburnated bone
41
small cracks in cartilage seen in the early stages of OA =
fibrillations
42
4 radiological features of OA =
Loss of joint space = cartilage loss Subchondral sclerosis = eburnation Subchondral cysts = Synovial fluid accumulation Osteophytes = disorganised bone remodelling
43
RA: AI process = ____ and so there are lots of ___
RF IgM - plasma cells that produce this
44
in RA ___ is destroyed by inflammatory process and ___ is formed = __+__
cartilage destroyed | pannus - inflammatory cells and hyperplastic synovium