Tumors Flashcards

IMC 606

1
Q

Histologic features of

Pilocytic astrocytoma

A

Biphasic
Rosenthal fibers [9c]
GFAP+ [9a]

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2
Q

Histologic features of

Infiltrating Astrocytoma

A

hypercellular
nuclear atypic
GFAP+

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3
Q

Histologic features of

Anaplastic astrocytoma

A

Hypercellular
nuclear atypic
GFAP+
**No microvascular proliferation of necrosis **

Bold is differentiator between this and an infiltrating astrocytoma

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4
Q

Histologic features of

Glioblastoma

A

Hypercellular
nuclear atypic
mitotic acitivity
GFAP+ [13f]
pseudo palisading necrosis [13e] sash
microvascular proliferation [13c] red hair beard moustache

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5
Q

Histological features of

Oligodendroglioma

A

“Fried egg” neuronal cell bodies (cytotoxic edema) [14e]
Chicken wire capillaries [14f]

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6
Q

Histologic features of

Ependymomas

A

Perivascular psuedorosettes [11f]
ependymal rosettes [11g]

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7
Q

Histologic features of

Meningiomas

A

Circumscribed [12d]
Spindle cells
Whorl pattern [12b]
Psammoma bodies [12f/18]

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8
Q

Histologic features of

Medullablastomas

A

Small roud cells
Homer-Wright rosettes [10i]

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9
Q

Histologic features of

Gangliogliomas

A

Binucleated ganglion cells
Peripheral Nissl substance
Glia
Calcifications

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10
Q

Glioma with WHO grade I

A

Pilocytic astrocytoma [9]

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11
Q

Glioma with WHO grade II

A

Infiltrating Astrocytoma
Oligodendroglioma [14]

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12
Q

Glioma with WHO grade III

A

Anaplastic Astrocytoma

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13
Q

Glioma with WHO grade IV

A

Glioblastoma [13]

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14
Q

Name this glioma

A

Pilocytic Astrocytoma [9c]

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15
Q

Name this glioma

A

Glioblastoma [13d]

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16
Q

Name this glioma

A

Glioblastoma [13e]

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17
Q

Name this glioma

A

Anaplastic Astrocytoma

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18
Q

Name this glioma

A

Oligodendroglioma [14e] [14f]

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19
Q

Name this glioma

A

Ependymoma [11]

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20
Q

Symptoms of

Pilocytic Astrocytoma

A

Cerebellar deficits [5] [6]

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21
Q

Symptoms of

Infiltrating Astrocytoma

A

New onset seizures

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22
Q

Symptoms of

Anaplastic Astrocytoma

A

New onset seizures
Headache
Focal signs

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23
Q

Symptoms of

Oligodenroglioma

A

Seizures [8]
Headache [10]
Focal signs [9]

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24
Q

Symptoms of

Ependymomas

A

Obstructive hydrocephalus [7]
Headache [2]
Vomiting [5]
Focal signs

25
Q

Symptoms of

Meningioma

A

Seizures [8]
Headache [10]
Focal Signs [9]

26
Q

Symtpoms of

Medulloblastomas

A

Obstructive hydrocephalus [7]
Headache [2]
Vomiting [5]
Ataxia [6]
Nystagmus
CN VI palsy

27
Q

Symptoms of

Gangliogliomas

A

Seizures

28
Q

What CNS tumors occur in the supratentorial region?

A

Infiltrating astrocytoma
Oligodendrogliomas
Pediatric CNS tumors: Pilocytic astrocytoma, medulloblastoma, ependymomas

29
Q

What tumors occur in the meninges

A

Meningioma [12]

30
Q

What CNS tumor occurs in the 4th ventricle in children?

A

Ependymoma [10]
Medulloblastoma [11]

31
Q

What CNS tumor occurs in the spinal cord in adults?

A

Ependymoma [11c]

32
Q

What tumors occur in the hemispheres of the cerebellum?

A

Glioblastoma
Ganglioglioma

33
Q

What glioma occurs in the CNS?

A

Anaplastic astrocytoma

34
Q

What glioma occurs in the brainstem?

A

Glioblastoma

35
Q

What gliomas are common in 30-45 year olds?

A

Infiltrating Astrocytoma
Anaplastic Astrocytoma
Oligodendrocytoma

36
Q

What gliomas are common in 8-13 year olds

A

Pilocytic astrocytoma [9]

37
Q

What brain tumors are common in children

A

Pilocytic astrocytoma [9]
Ependymomas [11]
Medulloclastoma [10]
Gangliogliomas

38
Q

What chromosomes/ proteins are involved in

Tuberous sclerosis

A

ch9- hamartin [15]
ch16- tuberin [14]

39
Q

What chromosomes/ proteins are involved in

Sturge Weber

A

ch9

40
Q

What genes are involved in

Tuberous Sclerosis

A

TSC1
TSC2

41
Q

Clinical features of

Tuberous Sclerosis

A

Skin lesions [24] [25] [26]
Seizures [22]
Intellectual disability [23]

42
Q

Clinical features of

Sturge Weber

A

Seizures [9]
Port wine birthmark [3]
Glaucoma [11]

43
Q

What gene is involved in

Sturge Weber

A

GNAQ [4]

44
Q

What is a Hamartoma?

A

Benign overgrowth of tissue

45
Q

What is a Tuber?

A

Enlarged gyri with disorganized lamination lacking separation between grey and white matter

46
Q

Pathology seen in

Tuberous Sclerosis

A

Hamartomas [15]
Cortical tubers [19]
Depigmented nevi
Angiofibromas
Subungual fibromas
Shagreen patches
Subependymal nodules
Subependymal giant cell astrocytoma

47
Q

Pathology seen in

Sturge Weber

A

Leptomeningeal angiomas [7]
Cortical calcifications with tram track appearance [13]

48
Q

Histological features of

Schwannomas

A

Biphasic
Areas with increased cell density (Antoni A) and lower density (Antoni B).
The Antoni A areas contain Verocay bodies, areas of palisading nuclei with an intervening non-nuclear region.

49
Q

How are schwannomas related to the genetic defect in neurofibromas

A

Defects in the NF-2 [17] gene on chromosome 22 [17b] code for the protein merlin [17a]. Merlin is a cell adhesion molecule that suppresses cell growth in crowded cellular environments. Defects in merlin allow uninhibited growth of Schwann cellsm [8].

50
Q

Where do schwannomas form?

A

along CN VIII and at the cerebellopontine angle [18]

51
Q

What are some symptoms of a schwannoma?

A

vertigo[18c], hearing loss [18b], tinnitus, ear fullness, nausea

52
Q

Chromosome affected in

NF1

A

ch17 [2b]

53
Q

Chromosome affected in

NF2

A

ch22 [17b]

54
Q

Protein affected in

NF1

A

Neurofibromin [4]

55
Q

Protein affected in

NF2

A

Merlin [17a]

56
Q

Inheritance of

NF1

A

Autosomal dominant [2]

57
Q

Inheritance of

NF2

A

Autosomal dominant [17]

58
Q

Symptoms of

NF1

A

Lisch nodules [7]
freckling
cafe-au-lait spots [6]
neuro-fibromas
optic nerve gliomas [11]
seizures
learning disabilities
bone deformities [16]

59
Q

Symptoms of

NF2

A

Schwannomas [8]
bilateral vestibular schwannomas [18]
cataracts [23a]
meningiomas [23]