Approach to the cancer cases Flashcards

1
Q

What is cancer?

A
  • An uncontrolled proliferation of abnormal cells
  • Independent of the requirement for new cells
  • Cellular differentiation is often impaired
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2
Q

Why do so many pets die of cancer?

A
  • Delayed / erroneous diagnosis
  • Failing to treat successfully
  • – Primary disease
  • – Metastatic spread
  • Ineffective treatment
  • Owner decides not to treat
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3
Q

What are principles of oncology?

A
  • Cancers do not go away
  • Know what you are treating
  • Work to understand owner goals
  • Treat early – for best chance of cure
  • Plan treatment well
  • – Mismanagement of case in early stages can often jeopardise later treatment success
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4
Q

What are signs of cancer?

A
  • Abnormal swelling that persists or cont. to grow
  • Sores that do not heal
  • Unexplained weight loss
  • Loss of appetite
  • Bleeding or discharge from any body opening
  • Bad odor, especially from the mouth
  • Difficulty eating or swallowing
  • Reluctance to exercise or loss of stamina
  • Difficulty breathing, urinating, defecating
  • Change in behavior
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5
Q

What can be used to diagnose cancer?

A
  • History
  • Physical examination
  • Minimum database (CBC, Biochem, UA)
  • Biopsy =
    • Cytology
    • Histology - Grading
  • Imaging
  • Immunochemistry, PCR, elecrophoresis
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6
Q

What history should be noted?

A
  • General - Diet, travel, medications
  • When was it noticed?
  • Behavioural information =
    • Size
    • Growth rate?
    • Changes in appearance?
    • Any other masses?
  • Other clinical signs / co-morbidities?
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7
Q

What should be done on clinical exam?

A

*Measure and record size and location of all lesions
*Assess invasiveness and attachment to underlying tissues
*Look for characteristics associated with malignancy

*General condition and BCS assessment =
* - Mentation
* - Palpation over the whole body for other lesions.
* - Palpation of lymph nodes especially draining nodes
* - Abdominal palpation
* - Assessment of CVS and respiratory systems.
*Depending upon clinical signs =
* - Palpation looking for signs of pain, especially over bones and spine.
* - Oral and rectal examination as appropriate
* - Mentation and neuro assessment

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8
Q

What are the advantages / disadvantages of cytology?

A

–Relatively non-invasive
–Often only physical restraint
–Minimal tissue disruption
–Rapidly performed
–Rapid results
–Cheaper
–No architectural detail
–Small numbers of cells examined = representative?
–Limited assessment of tumour
type/grade

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9
Q

What are the advantages / disadvantages of histopathology?

A

–More invasive
–GA (or sedation) required
–Moderate tissue disruption
–More time consuming
–Delay in results
–More expensive
–Architecture apparent
–Larger sample size = More representative
–More accurate tumour type/grade

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10
Q

What are contraindications for doing fine needle aspirates?

A
  • Bleeding
    • If platelet count normal and no evidence of coagulopathy then usually OK
    • I do not check PT / APTT prior to FNA unless problem suspected
    • Monitor patients afterwards
  • Risk of pneumothorax / urine / abscess leakage after
    sampling
    • Small but not inconsiderable = Pneumothorax after lung FNA ~ 20%
  • Risk of tumour transplantation deeper into tissue =
    • Take care not to go through lesion
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11
Q

What are problems with fine needle aspirates?

A
  • None diagnostic sample
  • Around 20% of samples
  • Always check if sending away
  • None representative sample
  • Especially heterogeneous lesion such as mammary tumours
  • Healing lesions – meaning of large fibroblasts?
  • Minimisation
  • Take several samples
  • Consider in context of patient and tumour
  • Keep monitoring the lesion
  • Bear in mind the strengths of cytology
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12
Q

What are different tissue biopsy techniques?

A
  • Needle core biopsy
  • Incisional biopsy
  • Surface and pinch biopsies
  • Punch biopsy
  • Excisional biopsy
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13
Q

What are risks of biopsy?

A
  • Haemorrhage
    – Internal organs – FNA check platelets OK, Trucut of internal organ check coags also
    – If there is evidence of bleeding check coags
  • Transplantation of tumour cells – Consider sampling path
  • Compromise of future surgery
  • Damage to adjacent structures
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14
Q

What are advantages of needle core biopsies?

A

*Larger sample than aspirate – Some evaluation of architecture
*Comparatively inaccessible tissues can be accessed percutaneously
*Multiple samples can easily be taken
*Superficial lesions can be biopsied under sedation and local anaesthesia

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15
Q

What are disadvantages of needle core biopsies?

A

*Small samples size compared to other biopsy
–Still might not be sufficient to view architectural change
*Greater risk of complications compared to FNA
–Esp for intracavitatory biopsies
*NOT GOOD FOR LYMPH NODES
–Insensitive to metastatic disease
–Inadequate for architectural assessment in lymphoma

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16
Q

What are advantages of incisional biopsy?

A
  • Good evaluation of architecture
  • Histopathological grading
  • Surgical approach allows selection of biopsy site
    – Trucut “blind”
    – Better sample, reduced risk
  • More tissue
    – Can carry out special stains etc
17
Q

What are disadvantages of incisional biopsy?

A
  • GA normally required
  • Increased time
  • Both increase costs
18
Q

What should be done with oncology monitoring?

A
  • Active monitoring or watchful waiting must be active
    – Only appropriate for benign lesions or after surgery were recurrence is unlikely
    – Many owners are not confident or cannot do this well
    – Nurse checks can be useful for this
    – Prompt and appropriate action
19
Q

What is the difference in stage + grade of tumour?

A
  • Stage = how far has it got = clinical assessment of current disease burden
  • Grade = histological features - activity, vascularity, invasion, necrosis, differentiation
20
Q

How do you clinically stage tumours?

A
  • Apply principles + basic knowledge of tumour biology
  • T = primary tumour
  • N = metastatic disease in local + regional lymph nodes
  • M = distant metastatic disease
21
Q

What is staging of T?

A
  • Clinical examination
  • Location and palpable extent – Well demarcated lesion?
  • Fixation – To deep tissues / – To skin
  • Ulceration
  • Contrast radiography
  • Ultrasonography
  • Endoscopy / laparoscopy / thoracoscopy
  • CT / MRI
22
Q

What tumours tend to spread via haematogenous (via circulatory system)?

A
  • sarcomas
  • Malignant melanoma
23
Q

What tumours tend to spread via lymphatic system?

A
  • Local + regional lymph node spread
  • Mast cell tumours
  • Carcinomas
  • Malignant melanomas
24
Q

Where do lymph node metastases go?

A
  • Spread to nearest node towards centre of body = towards thoracic duct
25
Q

How would you stage N (regional lymph node metastases)?

A
  • Palpation
    – Relatively insensitive to metastatic disease
    – Any palpable abnormalities – Size, Texture esp increased firmness, Fixation
  • Imaging
  • Cytology/histology - required for diagnosis
26
Q

What is lymphangiography?

A

– Detection of sentinel nodes using lymphangiography
– Inject contrast into the tumour to find out which nodes drain it
– Does not tell you if they are affected by metastases
– Only tells you which are draining nodes

27
Q

What are common sites for metastases? (M)

A
  • Lung
  • Parenchymatous organs (liver, spleen, kidneys)
  • Bone
  • Skin
  • CNS
  • Distant nodes
28
Q

With imaging what could you interpret as tumour in the liver?

A

Nodular hyperplasia = sample to confirm

29
Q

What should be done to check for metastases to parenchymatous organs?

A
  • Ultrasound + confirm with FNA
30
Q

What are limitations of the NM system?

A
  • Animals do not always present with the primary disease
  • Metastatic disease
    – Bony metastases
    – LN mets in tonsillar carcinoma
  • Paraneoplastic syndromes - can dramatically reduce patients life
31
Q

When would you refer tumours?

A

– Specialist expertise
– Advanced treatments
– Odd tumours / uncertain diagnoses
– Tricky clients
– More aggressive tumours
(most cases are managed well in general practice)

32
Q

What are highly metastatic tumours?

A
  • Oral/mucosal malignant melanomas
  • Visceral + soft tissue haemangiosarcomas
  • Appendicular osteosarcomas (dogs)
  • High grade Mast cell tumours
  • Subungual malignant melanoma (dog)
  • Poorly differentiated mammary tumours (dog)
  • Most mammary carcinomas in cats
  • (Anal sac adenocarcinoma)
  • (Prostatic carcinoma)
  • (Digital squamous cell carcinoma)
33
Q

What tumours are variably metastatic?

A
  • Oral /axial OSA
  • Thyroid carcinoma (dog)
  • Patnaik intermediate grade Mast Cell Ts
  • Injection site sarcoma
  • Anaplastic sarcoma
  • Insulinoma (most do!)
  • Mammary carcinomas (dog)
  • Apocrine adenocarcinomas
  • GIT carcinomas
  • Transitional cell carcinoma (TCC) of the bladder
  • Liposarcoma
34
Q

What are tumours with low metastatic potential?

A
  • Oral fibrosarcoma
  • Non-tonsillar oral squamous cell carcinoma
  • Most ST sarcomas
  • Sebaceous adenocarcinoma
  • Low grade MCTs
  • Multilobular osteoma /osteosarcoma of bone
  • Intranasal tumours
35
Q

What are tumours that don’t metastasise?

A
  • Oral acanthomatous ameloblastomas – Aka basal cell carcinomas or acanthomatous epulids
  • Haemangiopericytoma
  • Schwannoma/neurofibroma
  • BENIGN TUMOURS
36
Q
A