Spine Neoplasia Flashcards

1
Q

What are the most common intramedullary spine tumors?

A

Ependymoma (45%)
Astrocytoma (35%)
Hemangioblastoma (5%)
Others: Lipoma, Ganglioglioma

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2
Q

Spinal ependymoma: at what age do they peak?

A

Young adults

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3
Q

Spinal ependymoma: associated with what syndrome?

A

Neurofibromatosis 2

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4
Q

Spinal ependymoma: Natural history

A

Months to years of nocturnal pain, then sensory/motor loss, sphincter disturbance
Can also get central cord symptoms from syrinx formation

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5
Q

Spinal ependymoma: Prognosis

A

Good and recurrence low if complete resection is achieved

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6
Q

Spinal ependymoma: Treatment

A

Complete surgical resection

Adjuvant radiation if high grade or multiple recurrent lesions

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7
Q

Spinal ependymoma: Most important predictor of postop function

A

preop status

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8
Q

Spinal astrocytoma: what age group

A

90% in age

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9
Q

Spinal ependymoma: where are they most commonly located?

A

Cervical and filum (typically myxopapillary ependymoma)

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10
Q

Spinal astrocytoma: where are they most commonly located?

A

Thoracic and cervical

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11
Q

Spinal astrocytoma: Presentation/Natural history

A

Indistinguishable from ependymoma. 25% malignant in adult

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12
Q

Spinal astrocytoma: 5 year survival

A

50% for 5 year survival (low grade) - recurrences common

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13
Q

Spinal astrocytoma: Treatment

A

Surgical resection

Adjuvant radiation for multiple recurrent lesions

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14
Q

Spinal hemangioblastoma: what percent of spinal intramedullary tumors?

A

5%

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15
Q

Spinal hemangioblastoma: associated with what syndrome

A

Von Hippel Linda (in 1/3)

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16
Q

Spinal hemangioblastoma: What age of presentation

A

Mean age 30-40

17
Q

Spinal hemangioblastoma: Most common location

A

Thoracic or cervical

18
Q

Spinal hemangioblastoma: Most common presentation

A

Years of sensory deficit (proprioceptive pain 2/2 dorsal columns), then sensory/motor loss, sphincter

19
Q

Spinal hemangioblastoma: Prognosis

A

Good and recurrence low if complete resection is achieved

20
Q

Spinal hemangioblastoma: Treatment

A

Complete surgical resection

21
Q

Ganglioglioma: Prognosis

A

Slow progression. Treat like ependymoma

22
Q

What are the most common intradural extramedullary spinal tumors?

A

Meningioma (40%)
Schwannoma (30%)
Neurofibroma (10%)

23
Q

Spinal meningioma: peak age of onset

A

age 50, more common in women

24
Q

Spinal meningioma: multiple is associated with what syndrome

A

Neurofibromatosis 2

25
Q

Spinal meningioma: Presentation

A

Localized back pain or slow-onset myelopathy

26
Q

Spinal meningioma: Recurrence rate

A

5%

15% with subtotal resection (better than cranial prognosis)

27
Q

Spinal meningioma: Treatment

A

Total surgical excision

Radiotherapy for recurrences that cannot be completely excised or rare malignant forms

28
Q

Spinal schwannoma: peak age

A

30 years

29
Q

Spinal schwannoma: associated with what syndrome

A

Neurofibromatosis 2

30
Q

Spinal schwannoma: Presentation

A

80% with radicular pain

31
Q

Spinal schwannoma: Recurrence rate

A

5-10%

40% in NF2

32
Q

Spinal schwannoma: Treatment

A

Total surgical excision

33
Q

Spinal neurofibroma: sex predilection

A

None

34
Q

Spinal neurofibroma: Peak age of onset

A

age 20

35
Q

Spinal neurofibroma: what syndrome is it associated with

A

Neurofibromatosis 1 (60% with NF)

36
Q

Spinal neurofibroma: Presentation

A

80% with radicular pain

37
Q

Spinal neurofibroma: Recurrence rate

A

10-15% (malignant degeneration 5-10% in NF1)

38
Q

Spinal neurofibroma: Treatment

A

Total excision. Pain relief (85%) even with partial excision