Interpretation in pathology Flashcards

1
Q

What are pathological lesions?

A
  • are morphological changes in a tissue, caused by disease or trauma
  • this may be significant or incidental
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2
Q

Other changes can occur in tissues which may be confused with pathological lesions what are examples of these?

A
  • agonal changes (in and around the time of death)
  • post mortem changes
  • iatrogenic changes (clinical procedures)
  • variations in anatomy
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3
Q

What is gross pathology?

A
  • the recognition and description of macroscopic, morphological changes to tissues and organs in the live or dead animal at biopsy, surgical removal or post mortem examination (PME)
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4
Q

What are the 4 potential outcomes of gross pathology?

A
  • definitive diagnosis based on appearance alone
  • determine potential problem which may correlate with clinical signs an support a presumptive diagnosis
  • suggest pathogenesis or mechanism of a disease
  • changes not distinct enough to establish a diagnosis = further tests required
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5
Q

A pathologist needs to determine if the change is significant or incidental - what is a significant change?

A
  • contributed to pathogenesis/ clinical signs/ morbidity/ mortality in the case
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6
Q

What is an incidental change?

A
  • unrelated to the case, found as a result of the examination and/or sampling
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7
Q

Incidental changes may be related to signalment - what are examples of this?

A
  • species/strain/breed related changes
  • age related changes
  • sex related changes
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8
Q

Incidental changes may be coincidental findings - give an example of this:

A
  • discovering a neoplasia in an animal killed by a traumatic injury
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9
Q

How may be go about interpreting the significance of gross changes?

A
  • may need to undertake further examination such as histopathology (microscopic examination)
  • need to be interpreted in the context of the case history
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10
Q

What are agonal changes?

A
  • changes that occur at or around the time of death
  • often due to mechanism of death
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11
Q

What are examples of agonal changes from barbital euthanasia?

A
  • splenic congestion
  • pulmonary oedema
  • barbiturate crystals
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12
Q

What are post mortem changes?

A
  • changes to tissues that occur after death
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13
Q

Post mortem changes can vary depending on what?

A
  • the condition of the carcass at death
  • the environmental condition during the period between death and post mortem (post mortem interval, PMI)
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14
Q

What do post mortem changes need to be differentiated from?

A
  • need to be differentiated from pathological lesions
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15
Q

What things do pathologists need to know before PME?

A
  • the storage conditions of the body
  • environmental conditions, refrigerated, frozen, exhumed
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16
Q

What is algor mortis?

A
  • the cooling of the body after death
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17
Q

Algor mortis can vary due to what factors?

A
  • species = faster in smaller animals
  • site of temperature measurement
  • insulation = slower in animals with lots of hair/wool/adipose tissue
  • slower in herbivores (continued fermentation generates heat)
  • environmental temperature conditions
  • state of animal before death (haemorrhage, pyrexia, sepsis, activity before death, wounds)
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18
Q

What is rigor mortis?

A
  • contraction of the muscles after death
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19
Q

What causes rigor mortis?

A
  • due to the lack of ATP to allow the breakdown of crosslinking in muscle fibres
  • subsides with autolysis of the muscle
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20
Q

Where is rigor mortis absent?

A
  • in emaciated animals (lack of muscle mass)
  • or in very cold conditions (may be confused with freezing)
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21
Q

When is rigor mortis more rapid?

A
  • rapid if there is activity before death
    e.g., seizure, struggle
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22
Q

In what circumstance may rigor mortis be instantaneous?

A
  • electrocution
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23
Q

What is livor mortis?

A
  • the sinking of blood in vessels
  • can see body position when dead or if a body has been moved
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24
Q

In livor mortis how does blood pool?

A
  • pool sites are dependent due to gravity
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25
Q

The blood in livor mortis does what after a period of time?

A
  • eventually sets so the pattern will remain despite moving the body after death
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26
Q

What should you check to make sure your not seeing hypostatic congestion (livor mortis)?

A
  • should always check for symmetry when you see a colour change
27
Q

How would you differentiate between hypostasis (livor mortis ) and bruising?

A
  • bruising is outside the vessel
  • hypostasis is blood sinking in the vessel
28
Q

What are post mortem blood clots like?

A
  • will not be adhered to vessel walls and they form coasts of the vessels in which they are found
  • pale portion (chicken fat clot)
  • red portion (red current jelly clot)
29
Q

What are ante mortem thrombi like?

A
  • thrombi in arteries will be attached to the artery wall, are often dry and taper off in the direction of blood flow before death
  • venous thrombi may be attached to the vessel wall but may resemble post mortem clots
30
Q

What is bloating?

A
  • gaseous distension of the gastrointestinal tract due to the production of gas by microbial activity
31
Q

What problems can bloating cause in a PME?

A
  • can squish the organs and change what we are trying to interpret
32
Q

What is taphonomy?

A
  • the study of the processes that affect the decomposition, dispersal, erosion, burial and re-exposure of organism after, at and even before death
33
Q

What is autolysis?

A
  • breakdown of tissue as a result of enzymes contained within cells = self-digestion
34
Q

What is putrefaction?

A
  • breakdown of tissue by microbial action
35
Q

INFO CARD:

A
  • scavenging
  • desiccation and mummification
    = both forms of decomposition
36
Q

What are the classical stages of decomposition?

A
  1. fresh
  2. primary bloat
  3. activate decay
  4. advanced decay
  5. skeletonization
37
Q

What is desiccation and mumification?

A
  • loss of water from tissues exposed to air after death
38
Q

What body parts are most susceptible to desiccation and mummification?

A
  • eyes and mucous membranes
39
Q

What organ desiccates more slowly?

40
Q

What conditions are required for mummification?

A
  • can occur with low humidity and adequate ventilation
41
Q

What is forensic entomology?

A
  • predictable colonisation of a cadaver after death in different environments by different invertebrate life stages and species
42
Q

What is the best way to identify post mortem interval?

A
  • forensic entomology
43
Q

What can forensic entomologists provide?

A
  • advice for sampling - live and preserved samples
  • can be a data logger (left at the scene to provide data for interpretation)
44
Q

What are the limitation of forensic entomology?

A
  • educator of investigators - entomological evidence collection
  • absence of invertebrates in some cases or loss during body recovery
  • lack of environmental/meteorological data for a scene
45
Q

Biochemistry and microbiology is ongoing research what could it be used alongside or replace in the future?

A
  • forensic entomology
46
Q

INFO CARD:

A

Biochemistry:
- large number of parameters to choose from
- requires standardisation and validation

Microbiology:
- exciting prospects for PMI and other forensic applications

47
Q

What are pigments due to post mortem changes?

A
  • haemoglobin imbibition
  • bile imbibition
  • pseudomelanosis
48
Q

What is haemoglobin imbibition?

A
  • staining of tissues by haemoglobin pigment due to erythrocyte rupture after death
49
Q

What is bile imbibition?

A
  • staining of tissues by bile pigment leach out from the gall bladder after death
50
Q

What is Pseudomelanosis?

A
  • blue-green/green-black discolouration from hydrogen sulphide created by putrefying bacteria
51
Q

What is normal colour determined by?

A
  • innate colour and number of cells
  • special pigments
  • adipose tissue
  • amount of blood in the vascular bed
52
Q

What is the pigment : tissue ratio like in dark tissues?

A

= high pigment to tissue ratio

53
Q

What is the pigment : tissue ratio like in light tissues?

A

= low pigment : tissue ratio

54
Q

Pigments can be split into what?

A
  • endogenous
  • exogenous
55
Q

Haemorrhage (extravasation of RBCs), congestion, lysis of RBCs, and aging bruises can impart what pigment?

A
  • red-brown, green and yellow pigments to tissues (dependent on stage of process)
56
Q

What is icterus?

A
  • Staining of tissues yellow by bile pigments due to pre-, intra- or post-hepatic causes
57
Q

Some drugs can cause staining - give an example:

A
  • e.g. tetracycline discolouring developing teeth and bones
58
Q

How can fibrosis cause pigment loss?

A
  • Loss of tissue pigment due to replacement with fibrous connective tissue
59
Q

Melanin pigment may be present as part of normal colouration, in discrete areas (melanosis) - where can it be increased or decreased?

A
  • increased or decreased as part of some inflammatory changes, or tumours (melanoma)
60
Q

Fungi, bile, eosinophil infiltrates can cause what discolouration?

A
  • green discolouration to tissue
61
Q

Carotenoids can cause what discolouration?

A
  • Yellow discolouration to plasma and lipid laden cells
62
Q

where can tattoos, carbon and other dusts be found in the body?

A
  • Can be present in tissues and migrate to local lymph nodes