Spine Neoplasia Flashcards

(38 cards)

1
Q

What are the most common intramedullary spine tumors?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Spinal ependymoma: at what age do they peak?

A

Young adults

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Spinal ependymoma: associated with what syndrome?

A

Neurofibromatosis 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Spinal ependymoma: Prognosis

A

Good and recurrence low if complete resection is achieved

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Spinal ependymoma: Treatment

A

Complete surgical resection

Adjuvant radiation if high grade or multiple recurrent lesions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Spinal ependymoma: Most important predictor of postop function

A

preop status

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Spinal astrocytoma: what age group

A

90% in age

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Spinal ependymoma: where are they most commonly located?

A

Cervical and filum (typically myxopapillary ependymoma)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Spinal astrocytoma: where are they most commonly located?

A

Thoracic and cervical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Spinal astrocytoma: Presentation/Natural history

A

Indistinguishable from ependymoma. 25% malignant in adult

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Spinal astrocytoma: 5 year survival

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Spinal astrocytoma: Treatment

A

Surgical resection

Adjuvant radiation for multiple recurrent lesions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Spinal hemangioblastoma: what percent of spinal intramedullary tumors?

A

5%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Spinal hemangioblastoma: associated with what syndrome

A

Von Hippel Linda (in 1/3)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
Spinal meningioma: Presentation
Localized back pain or slow-onset myelopathy
26
Spinal meningioma: Recurrence rate
5% | 15% with subtotal resection (better than cranial prognosis)
27
Spinal meningioma: Treatment
Total surgical excision | Radiotherapy for recurrences that cannot be completely excised or rare malignant forms
28
Spinal schwannoma: peak age
30 years
29
Spinal schwannoma: associated with what syndrome
Neurofibromatosis 2
30
Spinal schwannoma: Presentation
80% with radicular pain
31
Spinal schwannoma: Recurrence rate
5-10% | 40% in NF2
32
Spinal schwannoma: Treatment
Total surgical excision
33
Spinal neurofibroma: sex predilection
None
34
Spinal neurofibroma: Peak age of onset
age 20
35
Spinal neurofibroma: what syndrome is it associated with
Neurofibromatosis 1 (60% with NF)
36
Spinal neurofibroma: Presentation
80% with radicular pain
37
Spinal neurofibroma: Recurrence rate
10-15% (malignant degeneration 5-10% in NF1)
38
Spinal neurofibroma: Treatment
Total excision. Pain relief (85%) even with partial excision