Cytology in practice Flashcards
advantages of cytology
quick, easy cheap
non-invasive
can be good diagnositic tool
limitations of cytology
relies on sample quality
exp of examiner
histopath
more expensive
slower - 48h
tumour grading
immunhistochemistry more avaiable
what/where to sample - aspiration or imprints
superficial masses
lymph node
organs, deep masses
what/where to sample - fluid
body cavities
joints
resp tract
cerebrospinal fluid
fine needle biopsy
solid + fluid filled masses visual/ultrasound guidance similar to FNA but no -ve pressure insert into mass several times - more representative necrotic centre - sample wall + centre
fine needle aspiration (FNA)
only if needle biopsy unrewarding
needle in centre of mass, apply -ve pressure
repeat 2-3x for representative sample
release plunger before removing needle
touch impression (imprints)
good for excised tissue/superficial lesions
made before excised tissue in put in 10% buffered formalin + submitted for histopathology
imprints
use fresh cut surface of tissue
blot till dry
imprint directly onto slide
4-5 imprints per slide
collection of fluid
clot prevention - EDTA
bacteriology - sterile pot
slide prep - fresh
inflammation vs neoplasia
sample mostly infl cells (WBC) or tissue cells (neoplastic)
if both, exp needed - one could be primary cause and the other secondary
septic inflammation
bacteria/organisms
degenerate neutrophils
bacteria intracellular within neutrophils to be significant
if extracellular - contaminants
non-septic inflammation
no bacteria/organisms
neutrophils non-degeneratie
no identifiable bacteria
degenerative change in neutrophils
nuclear change
nucleus swells, loses lobulation + paler
secondary to release of bacterial toxins
incr numbers of macrophages - causes
granulomatous infl - mycobacterium sp
if neutrophils also - pyogranulomatous infl - fungal
either can be seen with foreign bodies