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EQUINE CLINICAL PATHOLOGY - Rossdale & Partners

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G u i d e t o e q u i n e c l i n i c a l p a t h o l o g y<br />

of tissue is then removed to include both<br />

adrenal glands and the adjacent aorta,<br />

for overnight fixation, prior to dissecting<br />

out the coeliaco-mesenteric sympathetic<br />

nerve ganglia, which lie between the<br />

adrenal glands and the aorta, but which<br />

are less easy to find in fresh condition.<br />

The bladder and internal genitalia are then<br />

removed and examined. The diaphragm<br />

is then examined and opened to reveal the<br />

thoracic viscera. The ribs are separated<br />

through their costochondral junctions,<br />

the intercostal muscles are cut and the<br />

ribs are broken back over the horse’s<br />

back. The ‘pluck’ including the trachea,<br />

heart and lungs are then removed for<br />

examination. The thymus is examined and<br />

removed in immature horses. The head<br />

is removed through the atlanto-occipital<br />

joint and ideally sectioned longitudinally<br />

with a band saw. The brain, meninges,<br />

guttural pouches, paranasal sinuses, teeth,<br />

pharynx and larynx are then examined<br />

thoroughly. The limb joints are opened<br />

for examination of the synovial fluid and<br />

surfaces. If indicated by the clinical signs,<br />

the neck and back vertebrae are dissected<br />

out and opened for examination of their<br />

articulations and the spinal cord. It is clear<br />

that a satisfactory examination of the head<br />

and spine of an adult horse is difficult to<br />

achieve under field conditions.<br />

Samples for bacterial or viral examination<br />

should be collected from abscesses, areas<br />

of inflammation, body cavities or seared<br />

viscera, using sterile swabs and placed<br />

without delay into Amies’ charcoal or<br />

specific viral transport media.<br />

Fluid samples from abscesses, cysts or<br />

body cavity fluids should be aspirated<br />

with a sterile syringe and then submitted<br />

in sequestrene (EDTA) for a nucleated cell<br />

count, and fixed with a suitable fixative<br />

(e.g. cytospin fixation fluid) for specific<br />

cytological processing. Another undiluted<br />

and unfixed sample should be submitted<br />

in a sterile container or on a sterile swab<br />

in transport medium or ideally into blood<br />

culture medium for concurrent bacterial<br />

culture.<br />

Samples for histopathological processing<br />

and examination should be carefully<br />

selected to provide thin and small, but<br />

representative tissue wedges, and totally<br />

immersed in 10% formol saline. Large<br />

thick samples fail to fix adequately and<br />

histopathological examinations are then<br />

unnecessarily complicated by autolytic<br />

changes, abused tissues may be ruined by<br />

artefactual damage and unrepresentative<br />

samples may not include the primary<br />

pathological changes.<br />

It is often wise to retain appropriate samples,<br />

e.g. gastric and intestinal content, urine and<br />

cubes of liver and kidney, carefully labelled,<br />

frozen, in case toxicological studies are<br />

required at a later date.<br />

49

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