Brain Tumors Flashcards

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1
Q

What is the most common benign brain tumor in adults?

A

Meningioma is the most common primary brain tumor overall in adults, accounting for about 30-35% of primary brain tumors.

90% are benign.

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2
Q

What is this lesion?

A

A meningioma.

These are typically benign, slow-growing extra-axial tumor arising from the meningothelial cells of the arachnoid. It is the most common primary brain tumor in adults.

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3
Q

What is the typical demographic affected by meningiomas?

A

Meningiomas are more common in women, especially between the ages of 40-70 years, due to their association with hormonal factors (e.g., estrogen/progesterone receptor expression).

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4
Q

What are the common imaging features of a meningioma?

A

Extra-axial (external to brain parenchyma) and may have a dural attachment.

Dural-based mass with a homogenous enhancement.

Dural tail sign (thickening of the dura adjacent to the tumor).

Well-circumscribed, often compressing adjacent brain tissue.

Hyperdense on CT and highly vascular on imaging.

Increase in bone density due to infiltration of the overlying bone.

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5
Q

What is a common histopathologic finding in meningiomas?

A

Spindle cells concentrically arranged in a whorled pattern.

Psammoma bodies.

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6
Q

What are some important immunohistolochemical stains seen with meningiomas?

A

Vimentin (mesenchymal tissue marker).

S-100.

CD68 (histocytes).

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7
Q

Meningiomas are derived from what type of cell?

A

Arachnoid cell origin.

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8
Q

What are the typical clinical features of a meningioma?

A

Progressive headaches.

Focal neurological deficits (e.g., weakness, sensory changes).

Seizures (due to cortical irritation).

Symptoms of increased ICP: Nausea/vomiting, vision changes, personality changes.

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9
Q

What factors increase the risk of meningioma development?

A

Female gender (due to hormonal influence) in a 3:1 distribution.

Prior radiation exposure to the head.

Neurofibromatosis type 2 (NF2) - chromosome 22.

Neurofibromatosis type 1 (NF1) - chromosome 17.

MEN1 association.

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10
Q

How are meningiomas classified pathologically?

A

Grade I: Benign (most common).

Grade II: Atypical, more aggressive.

Grade III: Malignant, rare and highly aggressive.

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11
Q

Where do meningiomas tend to develop?

A

Parasagittal (20.8 %)

convexity (15%)

tuberculum sellae (13%)

sphenodial ridge (12%)

olfactory groove (10%)

falx cerebri (8%)

lateral ventricle (4%)

tentorium cerebelli (4%)

orbital (1%)

Spinal (1%)

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12
Q

A significant portion of meningioma can appear in what part of the body other than within the brain?

A

Along the spinal cord.

According to a 336 case series, the occurrence of spinal meningioma was ~1%.

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13
Q

How is a meningioma diagnosed?

A

Imaging: MRI with contrast to identify a dural-based mass and dural tail.

Biopsy: Needed only if imaging is inconclusive

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14
Q

How does meningiomas appear on the T1WI vs T2WI?

A

T1WI : isointense

T2WI : hypointense

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15
Q

What are the management options for meningiomas?

A

Observation: Small, asymptomatic tumors.

Surgical resection: First-line for symptomatic or growing tumors.

Radiation therapy: For incompletely resected or recurrent tumors.

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16
Q

In terms of management, at what size are meningiomas observed?

A

Less than 3 cm meningiomas are observed with repeat imaging every 3 to 6 months.

17
Q

When is neurosurgery (or radiation) necessary for a meningioma?

A

When more than 3 cm and symptomatic.

perform surgery +/- radiation.

18
Q

What complications can arise from untreated meningiomas?

A

Mass effect: Progressive neurological deficits, seizures, cerebral edema, obstructive hydrocephalus.

Increased intracranial pressure: Headache, vomiting, vision changes, personality changes.

Signs of malignancy: DVTs.

Risk of malignant transformation (rare).

19
Q

What is the prognosis for patients with meningiomas?

A

Most meningiomas are benign and have an excellent prognosis following surgical resection. Atypical and malignant meningiomas may recur and require additional treatment.