Module 7:CNS: Brain Tumors Flashcards

1
Q

This card deck will focus on the last topic of brain tumors. First are primary brain tumors, what are intrinsic vs extrinsic and supratentorial vs infratentorial?

A

Intrinsic: gliomas (astrocytic, oligodendroglial)
Extrinsic: meningiomas, schwannomas
Supratentorial in adults
Infratentorial in children

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2
Q

Secondary brain tumors are considered metastases, which is the most common brain tumor. What are the most common sources of these mets?

A
  1. Small cell lung cancer

2. Breast ( her 2 positive and triple negative)

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3
Q

What will the CT scan show for mets to the brain?

A

Multiple ring enhancing lesions in the cerebral hemisphere

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4
Q

Lymphoma is another common metastases to the brain, from what?

A

Esp in immunocompromised /HIV patients

–associated with multiple sexual partners

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5
Q

The first primary brain tumor to discuss is Glioblastoma Multiformes, what is the pathogenesis?

A

Most aggressive malignant tumor in the brain

  • -origin = glial cells/astrocytes
  • -high grade astrocytoma (Space occupying lesion) That spreads from one hemisphere (White matter) to the next through the corpus callosum
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6
Q

What is seen on gross and histology for a Glioblastoma Multiformes?

A

Butterfly appearance on gross
Located in the cerebral hemisphere (cross over at the corpus callosum)
Very hemorrhagic and necrotic
Histology: central area of necrosis surrounded by pseudo-pallacading of the malignant cells

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7
Q

What is the presentation for a Glioblastoma Multiformes?

A

Found in adults (40-60 yr olds)
–supratentorial
Sudden Onset
Recurrent headaches (Worse in the AM and while straining), seizures, papilledema, contralateral hemiparesis and projectile vomiting

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8
Q

What is the tumor marker for Glioblastoma Multiformes?

A

GFAP tumor marker (glial fibrillary acidic protein)

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9
Q

What is a poor prognosis for Glioblastoma Multiformes?

A

Infiltrate
Unresectable
Resistant to treatment

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10
Q

What is a better prognosis for Glioblastoma Multiformes?

A
Younger 
-EGFR
\+IDH-1
\+p53
\+MGMT methylation
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11
Q

What is the overall prognosis for patients with Glioblastoma Multiformes?

A

High grade astrocytoma (so patient dont live very long maybe a year)

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12
Q

The next brain tumor is an Oligodendroglioma, what kind of tumor is that?

A

Well differentiated glioma in 3rd and 4th decade

–indolent course and often calcified

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13
Q

What is the etiology for Oligodendroglioma?

A

Loss of heterozygosity for ch 1 & 19

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14
Q

What is the prognosis for Oligodendroglioma?

A

Good prognosis b/c chemosensitive

–better prognosis if 1p and/or 19q deletions

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15
Q

The next brain tumor is a Meningioma, what is the etiology?

A

Benign tumor with Benign Behaviors (slow growing and well circumscribed)

  • mostly sporadic and in older patients over 40
  • -if familial: associated with neurofibromatosis II NF2 (also associated with this is vestibuloschwannoma + meningioma)
  • -common in black women
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16
Q

What is the pathogenesis for a Meningioma?

A

Dome shaped tumor of the meningothelial cells of the arachnoid attached to the underside of the dura

17
Q

What are the signs and symptoms of a Meningoma?

A

Gradual onset
Headaches, Projectile vomiting and papillemdema
Seizures (irritates the cerebral cortex)

18
Q

What is seen on CT and excisional biopsy (Best investigation) for a patient with a meningoma?

A

See calcifications on CT: psammoma bodies

Excisional Biopsy: papillary projection (Whorled pattern of cell growth) with psammoma bodies

19
Q

What are the complications associated with a meningioma?

A

Complications: Compression of the cerebellar hemisphere — focal neuro deficits, cranial nerve problems and seizures
High degree of recurrence after removal but good prognosis

20
Q

There are two types of Nerve Sheath Tumors, neurofibroma and schwannoma. What are some features of a schwannoma?

A

Middle aged and elderly (earlier in NF2)

Slow growing tumor that arises from Schwann Cells

21
Q

Schwannoma most commonly affects, what?

A

CNVIII: acoustic neuroma

Spinal Sensory nerve roots

22
Q

Nerve sheath tumors are cured by what?

A

Resection (Risk to perent nerve function)

23
Q

The next brain tumor is seen in kids called a Pilocytic Astrocytoma, what are some features?

A

Most common primary CNS tumor in childhood
–well differentiated glioma in the cerebellum & hypothalamus (composed of compactly and loosely arranged delicate hair like astrocytes)

24
Q

What is seen on CT/MRI in a patient with a pilocytic astrocytoma?

A

Cystic with enhancing rim and mural nodule

25
Q

How is pilocytic astrocytoma cured?

A

Resection

26
Q

The last brain tumor for this section is a Medulloblastoma, who is this seen in and what is the origin?

A

Seen in Children
–intratentorial
Origin: Cerebellar Vermis (can co-exist with Ewings tumor)

27
Q

What is seen on presentation for patients with Medulloblastoma?

A

Cerebellar Signs (ataxia, slurred speech, intention tremor, nystagmus, 3Ds)

28
Q

What is seen on histology for a medulloblastoma?

A
Excisional Biopsy (Best investigation): 
--homer-wright rosettes (pseudorosettes) - small round blue cells
29
Q

What are the complications of a Medulloblastoma?

A

Malignant tumor — spreads via CSF — spreads to ventricles – hydrocephalus (obstructive or non communicating)
Drop Metastasis: tumor cells detach, enter ventricles (Can reach cauda equina — cauda equina syndrome and nerve pain)

30
Q

What is the prognosis for a Medulloblastoma?

A

Radiosensitive
-risk of papillary thyroid cancer
Beta-Catenin positive so good prognosis

31
Q

If Medulloblastoma is familial what diseases is it associated with?

A

Tuckers

Ghorlin