Neuro - Pathology (Brain Tumors & Herniation Syndromes) Flashcards

Pg. 488-489 in First Aid 2014 Pg. 447-448 in First Aid 2013 Sections include: -Adult primary brain tumors -Childhood primary brain tumors -Herniation syndromes

1
Q

What are 6 examples of adult primary brain tumors?

A

(1) Glioblastoma multiforme (grade IV astrocytoma) (2) Meningioma (3) Hemangioblastoma (4) Schwannoma (5) Oligodendroglia (6) Pituitary adenoma

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2
Q

What is another name for glioblastoma multiforme? Describe the tumor: Is it common or rare? Is it benign or malignant? What is the median survival of patients with it?

A

Grade IV astrocytoma; Common, highly malignant primary brain tumor with ~ 1 year median survival

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3
Q

Where in the brain is glioblastoma multiforme (grade IV astrocytoma) found? To where can it expand, what is that called?

A

Found in cerebral hemispheres. Can cross corpus callosum (“butterfly glioma”)

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4
Q

What stain is used in glioblastoma multiforme, and for what cells?

A

Stain astrocytes for GFAP.

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5
Q

Describe the tumor cells seen in glioblastoma multiforme (grade IV astrocytoma).

A

“Pseudopalisading” pleomorphic tumor cells - border central area of necrosis and hemorrhage.

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6
Q

Describe a meningioma: Is it common or rare? Is it benign or malignant?

A

Common, typically benign primary brain tumor

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7
Q

Where in the brain do meningiomas most often occur?

A

Most often occurs in convexities of hemispheres (near surfaces of brain) and parasagittal region

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8
Q

From what kind of cells does a meningioma typically arise? What is the involvement of brain parenchyma and dura?

A

Arises from arachnoid cells, is extra-axial (external to brain parenchyma), and may have a dural attachment (“tail”)

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9
Q

How does meningioma often present? What are other ways in which it might present?

A

Often asymptomatic; may present with seizures or focal neurological signs

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10
Q

What are 2 defining characteristics of meningioma on histology?

A

Spindle cells concentrically arranged in a whorled pattern; psammoma bodies (laminated calcifications).

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11
Q

What is the treatment/management in meningioma?

A

Resection and/or radiosurgery.

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12
Q

Where in the brain is hemangioblastoma most often found?

A

Most often cerebellar;

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13
Q

With what condition is hemangioblastoma associated, and in what clinical context?

A

Associated with von Hippel-Lindau syndrome when found with retinal angiomas

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14
Q

What substance can be produced by hemangioblastoma, and what result does this have?

A

Can produce erythropoietin –> secondary polycythemia

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15
Q

What characterizes hemangioblastoma on histology?

A

Closely arranged, thin-walled capillaries with minimal interleaving parenchyma.

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16
Q

Where in the brain is Schwannoma usually found?

A

Usually found at cerebellopontine angle

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17
Q

From what cell does a Schwannoma originate? What can be used to test this? What is a common example of Schwannoma localization and its result?

A

Schwann cell origin, S-100 (+). Often localized to CN VIII –> acoustic schwannoma (aka acoustic neuroma)

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18
Q

What is the treatment/management for schwannoma?

A

Resectable or treated with stereotactic radiosurgery.

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19
Q

In what condition are bilateral acoustic schwannomas found?

A

Bilateral acoustic schwannomas found in NF-2.

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20
Q

Is oligodendroglioma common or rare? Is it fast or slow growing?

A

Relatively rare, slow growing

21
Q

Where is oligodendroglioma most often found?

A

Most often in frontal lobes

22
Q

What describes the capillary pattern in oligodendroglia? How do its oliogodendrocytes appear on histology?

A

Chicken-wire capillary pattern. Oligodendrocytes = “fried egg” cells - round nuclei with clear cytoplasm.

23
Q

What (imaging) finding is often present in oligodendroglioma?

A

Often calcified in oligodendroglia.

24
Q

What is the most common pituitary adenoma?

A

Most commonly prolactinoma

25
Q

What is the main clinical finding in pituitary adenoma, and why? What are 2 options for other sequelae with pituitary adenoma?

A

Bitemporal hemianopia due to pressure on optic chiasm. Hyper- or hypopituitarism are sequelae.

26
Q

What are 4 examples of childhood primary brain tumors?

A

(1) Pilocytic (low-grade) astrocytoma (2) Medulloblastoma (3) Ependymoma (4) Craniopharyngioma

27
Q

Describe the form/appearance of pilocytic (low-grade) astrocytoma.

A

Usually well circumscribed.

28
Q

Where in children is a pilocytic (low-grade) astrocytoma most often found? What is another region in which it may be found?

A

In children, most often found in posterior fossa (e.g., cerebellum); May be supratentorial

29
Q

What marker is positive in pilocytic (low-grade) astrocytoma?

A

GFAP (+)

30
Q

Is pilocytic astrocytoma benign or malignant? What kind of prognosis does it have?

A

Benign; good prognosis

31
Q

Name and describe the fibers that characterize pilocytic astrocytoma on histology. Briefly describe its gross apearance.

A

Rosenthal fibers - eosinophilic, corkscrew fibers; Cystic + solid (gross)

32
Q

What kind of tumor is medulloblastoma, in terms of benign/malignant and location? What is an embryological connection to make to this tumor?

A

Highly malignant cerebellar tumor; A form of primitive neuroectodermal tumor

33
Q

What condition can result from medulloblastoma, and why?

A

Can compress 4th ventricles, causing hydrocephalus.

34
Q

How does medulloblastoma metastasize?

A

Can send “drop metastases” to spinal cord

35
Q

What is the main histologic/gross finding to associate with medulloblastoma? How is medulloblastoma characterized on histology versus gross appearance?

A

Homer-Wright rosettes. Solid (gross), small blue cells (histology).

36
Q

Where are ependymal cell tumors most commonly found? What complication can result from this?

A

Ependymal cell tumors most commonly found in 4th ventricle. Can cause hydrocephalus.

37
Q

What kind of prognosis does ependymoma have?

A

Poor prognosis.

38
Q

What 2 findings characterize ependymoma on histology?

A

Characteristic perivascular rosettes. Rod-shaped blepharoplasts (basal ciliary bodies) found near nucleus.

39
Q

From where is craniopharyngioma derived?

A

Derived from remnants of Rathke pouch.

40
Q

What kind of tumor is craniopharygioma? With what can it be confused, and why?

A

Benign childhood tumor, may be confused with pituitary adenoma (both can cause bitemporal hemianopia).

41
Q

What is the most common childhood supratentorial tumor?

A

Craniopharyngioma

42
Q

What (imaging) finding is common in craniopharyngioma? What is a descriptor for this finding?

A

Calcification is common (tooth enamel-like)

43
Q

What are the 4 key herniation syndromes in neurology?

A

(1) Cingulate (subfalcine) herniation under falx cerebri (2) Downward transtentorial (central) herniation (3) Uncal herniation (4) Cerebellar tonsillar hernation into the foramen magnum

44
Q

Draw a visual, including arrows and labels for the following key herniation syndromes: (1) Cingulate (subfalcine) herniation under falx cerebri (2) Downward transtentorial (central) herniation (3) Uncal herniation (4) Cerebellar tonsilar herniation into the foramen magnum.

A

See p. 489 in First Aid 2014

45
Q

What is a significant vasculature concern in the context of cingulate (subfalcine) herniation under falx cerebri?

A

Can compress anterior cerebral artery

46
Q

Where is the uncus located?

A

Uncus = medial temporal lobe

47
Q

What 3 structures may be compressed in the context of uncal herniation? What effects does their compression have?

A

Compresses (1) ipsilateral CN III (blown pupil, “down-and-out” gaze), (2) ipsilateral PCA (contralateral homonymous hemianopsia), (3) contralateral crus cerebri (ipsilateral paralysis, “false localization” sign)

48
Q

What is a significant complication of cerebellar tonsil herniation into the foramen magnum, and why?

A

Coma and death result when these herniations compress the brain stem (and inhibit respiration)