Mast Cell Tumour + Transitional Cell Carcinoma Flashcards

1
Q

What are canine mast cell tumours?

A
  • Most commonly diagnosed skin tumour in the dog (16-21%).
  • Other sites = subcutaneous tissue, conjunctiva, oral mucosa, GIT.
    *Very variable behaviour
  • Various treatments available which need to be tailored to each case
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2
Q

What is presentation of MCTs? risk factors?

A
  • Unknown aetiology
  • Any age and no sex predilection
  • Breed predispositions e.g. Boxer, Boston terrier.
  • Sharpei get high grade MCTs
  • Variable biological behaviour
  • Invasiveness of primary tumour
  • Metastatic rate 10->90%
  • local lymph nodes
  • spleen and liver
  • Cutaneous masses of variable appearance - erythema, oedema, pruritus, haemorrhage
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3
Q

How are MCTs diagnosed?

A
  • FNA of the mass = Usually diagnostic (92-96%), Round cells, Characteristic purple granules
  • Diff Quick usually fine - Occasionally need special stains (eg toluidine blue)
  • For some poorly differentiated = biopsy +/- IHC required
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4
Q

What can be done to stage MCTs?

A
  • Abdominal US - assess liver, spleen, LNs, (FNA)
  • Thoracic radiography - lung metastasis, comorbidities
  • Buffy coat - non-specific + greater in inflammatory disease (when spun bloods - WBCs)
  • Bone marrow aspirates - rare unless extensive disease
  • Biopsy - FNA inconclusive, pre-surgical to determine grade
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5
Q

What does prognosis of MCTs depend on?

A

Clinical:
* Location eg Nail bed, oral, muzzle, prepuce, perineum, mucocutaneous junction.
* Breed (Sharpei vs boxer)
* Appearance
* Systemic illness
* Recurrence
* Clinical staging (i.e. presence of metastatic disease)
Laboratorial:
* Tumour histological grade (Most important)
* Other =
- Ki67
- AGNORs
- C-kit mutation
- Kit staining pattern

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6
Q

What is the PATNAIK grading system?

A
  • Most important prognostic factor - 3 grades
  • Grade I / well differentiated tumours = Benign behaviour (<10% metastasise), Low recurrence rates, Unlikely to cause death (up to 7-12%)
  • Grade II/ intermediate tumours = Variably metastatic (5-22% metastasise), Cause of death in 17-56% of patients, Nodal metastases associated with poorer prognosis in some studies but not in all
  • Grade III/ poorly differentiated tumours = Highly metastatic (>80%), Likely to be cause of death
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7
Q

What is the KIUPEL grading system?

A
  • 2 groups = low + high grade
  • Median survival time
    – less than 4 months for high-grade MCT
    – more than 2 years for low-grade MCTs
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8
Q

What is treatment of MCTs?

A
  • Multimodal Tx needed
    Surgery =
  • Margins
  • 3cm margins & 1 fascial plane
  • 1-2cm lateral margins may be adequate for grade I and II tumours
  • Histopathology - all excised masses; grade and margins
  • Grade I and II - Potential to be curative
  • Grade III - Still a role but not as sole modality
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9
Q

What occurs if incomplete margins after surgery?

A
  • 23% incompletely excised grade II recur
  • 5-11% completely excised recur
  • ~25% cases re-excision of scar reveals no mast cells
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10
Q

What should be done after surgery?

A
  • Radiotherapy - postop - incomplete excision / local nodal metastasis / gross disease - degranulation
  • Chemotherapy - high grade +/or confirmed mets, residual microscopic disease (Vinblastine/prednisolone)
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11
Q

What is seen with Feline MCT?

A

Cutaneous form
* Second most common cutaneous tumour in the cat (20%)
* Cutaneous raised hairless masses. Easily diagnosed by cytology and rarely metastatic. Multiple tumours.
* Surgical excision is usually curative (even marginal).

Visceral forms
* Splenic: Most common differential for splenic disease. Clinical signs of systemic disease. Staging is recommended. Splenectomy is the treatment of choice even if involvement of other organs. Unclear role of chemotherapy.
* Intestinal: Third most common intestinal tumour. Signs of GI and systemic disease and palpable abdominal mass. Metastasis are common. Poor prognosis

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12
Q

Where do animals get transitional cell tumours? Can the metastasise, if so where?

A
  • Urinary bladder - Trigone
  • Urethra + prostate in males
  • High metastatic rate
  • Common mets to medial iliac lymph nodes + other organs - liver, spleen, bones
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13
Q

What are clinical presentation of Transitional cell tumours?

A
  • Low urinary tract signs (haematuria, stranguria, pollakiuria).
  • Occasionally signs related with bone metastasis (lameness) or renal dysfunction.
  • Signs can be present for months as dog gets treated for “complicated UTIs”.
  • Signs may improve with courses of antibiotics
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14
Q

How are TCTs diagnosed?

A
  • Histopathological diagnosis although sometimes cytology very suggestive.
  • Risk of seeding with FNA
  • Traumatic catheterization/ prostatic wash
  • Cystoscopy (mainly females)/ surgical biopsy
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15
Q

What can you use to stage TCTs?

A

** Haematology/ Biochemistry/Urine analysis (including culture) **
- May show neutrophilia, renal dysfunction, presence of UTI
- Rule out any other problems and suitability for subsequent therapies

** Abdominal ultrasound **
* Assess bladder wall, urethra, prostate and kidneys +/- metastasis in other organs.
* FNA.
**n T&A radiography **
* Lung metastasis uncommon
* Bone metastasis

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16
Q

What is Tx of TCTs?

A
  • Surgery rarely possible due to location
  • External beam radiotherapy = High rate of complications
  • Brachytherapy = Suitable for prostatic and urethral tumours with improved survival.
  • Medical treatment =
  • NSAIDs alone MST 181 days
  • Mitoxantrone and NSAIDs MST 291 days
  • Other chemotherapy drugs (Vinblastine, chlorambucil, carboplatin etc.)
  • Palliative care =
  • Regular urine cultures and antibiotic courses as appropriate
  • Cystotomy tubes/ Urethral stents
17
Q

What is prognosis of TCTs?

A
  • Poor long term prognosis but quality of life can be maintained for several months.
  • Local disease most likely cause of death/euthanasia (MST 6-8 months).
  • Rapid deterioration due to renal failure or clinical signs associated with bone metastasis (pain) also possible
18
Q
A