export_final exam anat path rd 610 Flashcards

1
Q

most common underlying causes of sudden death in dogs:

A
  1. heart dz (DCM, HCM)
  2. Toxins (strichnine)
  3. GI- volvulus, torsions, parvo
  4. trauma- HBC
  5. Hemorrhage not assoc. with trauma (HSA)
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2
Q

**how often is sudden death reported as “undetermined” with path?

A

12.6%!

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3
Q

was malnutrition high as a cause of sudden death?

A

yes, surprisingly (higher than CNS)

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4
Q

top 5 sudden death killers in cats:

A
  1. trauma*
  2. heart dz
  3. intestinal
  4. resp*
  5. urinary tract dz*
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5
Q

how often was sudden death in cats “undertermined”

A

same as dogs- about 12.7%

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6
Q

unique about cats with intestinal sudden death (assoc. with and age)

A

most assoc. with feline panleuk and 6months

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7
Q

best indiv to sample

A

cohort with sim signs as other, best if early in the dz and not treated yet

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8
Q

before euthanizing, do this

A

collect blood samples

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9
Q

humane euthanasia:

A

capitve bolt + KCl

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10
Q

early steps in field necropsy

A

reflect skin, front and rear limbs, tongue, larynx, abdominal adn thoracic walls

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11
Q

position animal in___ and incise where

A

left lateral- incsie ventra midline lower lip-pubis

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12
Q

after incising, do what:

A

relfect limbs dorsally (cut pectorals and medial thigh muscles)

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13
Q

after reflection of limbs, examine

A

tongue, larnx, pharynx, esophagus, trachea

-pull tongue cadual until hyoid app adn cut through joint

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14
Q

after tongue-hyoid, do what

A
  1. open abd cavity (via caudal to last rib)
  2. cut dorsal attachments of greater omemntum
  3. expose thoracic viscera via cutting diaphragm along costal arch insertion
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15
Q

when thoracic and abd cavities open, do what?

A

sample for micro

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16
Q

how examine heart

A
  1. cut posterior VC-dorsal border of RA- RAuricle
  2. cut through AV orfice and tricuspid valve- extend to apex of ventricle
  3. flip heart dorsally, cut up thru free wall (adj to septum) through pulmonary valves into pulm trunk
  4. pulm veins- tip of left auricle
  5. lumen of ventricle, cut thru mitral valve and left vent wall to apex
  6. through aortic valve to arch
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17
Q

after examining heart and lungs, check out

A

urogenital- start with right kidney by disecting it free

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18
Q

when are pancreas, liver, LN, GB, bile ducts examined

A

after urogenital via serial bread loaf cuts

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19
Q

the intestine and forestomachs evulated when?

A

after hepatic parenchyma

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20
Q

import. to spot check where on intestine:

A

duodenum

jejunum

ileum

ileo-cecal jnct

cecum

LN

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21
Q

where are Peyer’s patches in LA

A

few meters aboral jejunum

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22
Q

where sample CSF?

A

through exposed dura mater at ventral a-o membrane (flex head)

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23
Q

when use water P to shell our brainstem and cerebellum?

A

TSE surveillance

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24
Q

formalin vs fresh tissue size

A

formalin: 0.5-1cm

fresh tissues: at least 3cm

25
do not use these to submit fluids or swabs if want bacterial culture
EDTA tubes b/c bacteriocidal
26
min sample for infectious GI disease includes:
loops of intestine for virology and bacteriology & colonic for parasitology
27
where swab for suspect meningitis
sella turcica
28
submit what with rabies concern:
entire cerebellum and brain stem- fresh
29
suspect TSE: submit
obex (fresh, chilled)- all ruminants
30
if suspect TSE in cervids and sheep submit:
- brainstem - retropharyngeal LN and tonsils (all fixed)
31
if suspect tox- submit
feed, water, abomasum, rumn, urine, fat, liver, kidney, brain, serum (spun down)
32
if want to pursue organic intox- do what with sample
wrapped in foil
33
can you freeze tox specimens?
yes- most
34
t/f diagnostic specimens are considered hazardous, regardless
true
35
ok to have specimens in ziplock bags
no- only as second package
36
Biological Specimen- Cat B; UN3373 means
specimens may contain pathogenic org could cause dz in people or animals
37
list reasons to bx skin:
- suspect neoplasia - non-responsive to tx - derm signs suspect dt internal causes - chronic ulcerative lesions - if therapy is $ or time-consum - only diff way to dx - lesions in unusual sites
38
most common non-dx lesions to avoid bx
chronic purritic allergic derm or parasitic derm (=epidermal hyperplasia and mixed perivascular inflamm)
39
dx of parasitic dz made how
skin scrapings or treatment trials
40
if suspect 2nd lesions then:
tx infection and bx later when infection resolved
41
list primary lesions:
macule, papule, plaques, pustules, vescicles, bullae, wheals, nodules, tumors, cysts
42
secondary lesions evolve from: (2)
self-trauma or medications
43
list secondary lesions:
-epidermal collarettes, scars, erosions, ulcers, fissures, lichenification
44
can secondary lesions, although less specific, help help with dx
yes, just don't use as sole lesion
45
are hyperpig and lichenification specific?
no! 
46
alopecia, scale, crusts, follicular casts, comedones, hyperpig, hypopig can all be
primary OR secondary
47
2 sizes of punch bx and when use either
6mm standard 4m- face, more delicate areas
48
should punch bx include significant amnt of normal?
no
49
rotate punch how?
one direction only
50
do what with punch bx specimen to prevent curling?
blot and remove fluid then place on tongue depressor or cardboard for 1-2 mins, then put both in formalin
51
list things to report to pathologist:
- hx- age onset, progression of signs, response to meds* - PE and lesion types - distribution of lesions - list of supect differentials
52
IHC=
- tissues are incubated with Ab's for cell marker in question - binding of primary Ab is detected by using a specific secondary Ab= colored reaction
53
case hx you want to get with suspect toxicosis
- breed, sex, age, wt - prev med hx, current meds - # in grp, #exposed, #exhib signs - type, duration, severity of signs - time of exposure - dosage - agent formulation
54
common antemortem samples for toxicology
- whole blood, serum, urine - stomach contents - hair* - suspect material - feed, water
55
whole blood in:
EDTA
56
serum analysis use this tube
royal blue- red top tubes can mislead zinc levels
57
only antemortem test that can't be both refridgerated and frozen:
whole blood in EDTA
58
list PM samples
- liver, stomach contents, bile - abd fat - kidney, urine - brain, eyeball - heart clot blood, serum
59
why does quantification pose challenge to toxicologists?
- lack of hx information, tissue selection, and sample quality - time frame from exposure to sampling