0513 - Tumours of the CNS Flashcards

1
Q

What is a single unique feature of CNS neoplasms?

A

They don’t metastasize outside CNS even when malignant - so need a separate definition of benign and malignant. Instead it kills by compression of vital functions (loss of function) or raised intracranial pressure.

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2
Q

Where are Neurons, Oligodendrocytes, and Ependymal cells (and their respective tumours) found?

A

Neurons - Grey Matter
Only oligos - White Matter
Ependymal cells - Near ventricles

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3
Q

What proportion of CNS tumours are primary vs metastasis?

A

25% Primary

75% Metastases

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4
Q

What are some presenting complaints of brain tumours?

A
Headache
Personality changes/psychosis
Seizures
High intracranial pressure
Premature puberty
Raised prolactin (brainstem compression)
Sudden Death (haemorrhage, coning)
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5
Q

How is malignancy determined with brain tumours? (KEY EXAM CONCEPT)

A

Not based on metastases, based on micro appearance. WHO Grading.
A - Atypia (nasty nuclei)
M - Mitoses (even 1 is bad)
E - Endothelial Proliferation (occurs near the tumour)
N - Necrosis (= bad)

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6
Q

Outline the WHO grading system of astrocytomas

A

Grade 1 - Circumscribed, mild increase in cellularity, can be resected. Won’t grow back, grade stable.
Grade 2 - Moderate increase in cellularity, but margins poorly defined or diffuse. May grow back, grade unstable.
Grade 3 - Increased cellularity, moderate pleomorphism and mitosis. Worse than 2.
Grade 4 - Very marked pleomorphism, microvascular proliferation and/or palisading necrosis. The worst.

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7
Q

Briefly outline Astrocytoma

A

80% of all adult primaries and found in cerebral hemispheres. >40 generally.
Present with seizures, headaches, and focal deficits related to site.
Named according to grade.

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8
Q

What are the different names of astrocytoma according to grading?

A

1 - Pilocytic astrocytoma
2 - Diffuse astrocytoma
3 - Anaplastic astrocytoma
4 - Glioblastoma multiforme

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9
Q

What are the different types of Astrocytoma?

A
Diffuse/fibrillary astrocytoma (most common)
Pilocytic Astrocytoma (children and young adults) - best one to have
Glioblastoma Multiforme (most aggressive, older adults)
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10
Q

Outline Pilocytic Astrocytoma

A

Most common in cerebellum. Affects young children.
Grade 1, slow growing, good prognosis with surgery only.
Piloid gliosis (reactive astrocytes (scar) around tumour) and eosinophilic granular bodies.

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11
Q

What are the most important prognostic factors for Astrocytoma?

A

Age - inversely proportional to survival time
Tumour grade - but it can get worse
Any necrosis or incomplete resection is very bad.
Prognosis - 1-2 years.

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12
Q

Outline Oligodendroglioma

A

5-15% of gliomas
Most common >40
Slow growing, progress over several years.

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13
Q

How can you tell histologically that it’s an oligodendroglioma

A

Delicate ‘chicken wire’ vessels around in stroma.

Cells look like fried eggs - round nuclei and surrounding halo.

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14
Q

What is the most important factor in Oligodendroglioma prognosis?

A

1p and 19q deletion is diagnostic of the category.

If you don’t have it, probably not an oligo, but it will be refractory to treatment.

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15
Q

Outline Ependymoma

A

3-19% of gliomas. Occurs in adults and children
Arise from lining of ventricular system and spinal cord.
Present with symptoms relating to CSF obstruction. CSF dissemination is common.
Histology - makes canals (rosettes), with nuclei away from the lumen)

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16
Q

What are the 3 possible broad causes of raised ICP

A

Blood
Mass
CSF (too much, blocked)

17
Q

Outline Medulloblastoma

A

Highly malignant but very sensitive to radiation. Massive therapy required, but survivable.
Cells form rosettes - very primitive neurons but don’t look like it.
Occurs in all age groups.

18
Q

Outline Meningioma

A

20% of intracranial primaries.
Aged >40, F>M
Attached to dura and grows into cranial cavity.
Microscopy - Whorls of meningothelial cells, Psammoma bodies (pearls of calcium)

19
Q

What stain can be used when determining a glioma?

A

GFAP - Glial Fibrillary Acidic Protein