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SPINAL CORD TUMORS 
BY : DR / AHMED MOHAMMED DEBES 
NEUROSURGERY RESIDENT AT AHMED MAHER TEACHING HOSPITAL 
CAIRO, EGYPT. 
TUESDAY 09/10/2014
Spinal Cord Tumors 
Intra-dural 
Extra-dural 
Intra-medullary Extra-medullary
Extra-medullary 
Nerve Sheath 
Tumors 
Meningioma 
schwannomas neurofibromas 
s 
Filum Terminale 
Ependymomas 
• Gross 
• Micro 
• Asso. 
Neurofibromas 
• Fusiform 
• Fibrous tissue + 
nerve fibers 
• Neurofibromatosis 
type I 
Schwannomas 
• globoid masses, 
suspended eccentrically 
• Antoni-A(elongated 
cells) Antoni-B(stellate-shaped 
• schwannomatosis
• 4th – 6th decade , male = female 
•Mostly affect dorsal root 
most common 
30% 
(cervical) 
10% 
1%
arachnoid cap 
cells 
decade , 
•Mainly , upper 
cervical spine and 
foramen magnum 
•ventral or ventrolateral, 
may 
•10% 
•Do not penetrate the 
pia
decade , 
•Myxopapillary 
ependymomas 
•Cuboidal cells surrounding a 
vascularized core of 
hyalinized connective tissue 
•Benign
neural crest, benign, 
neurosecretory granules 
dumbbell tumors in 
pediatric 
thoracic spine 
rarely 
cause mass effect 
CSF drop metastases, 
direct penetration of the 
dural root sleeve
•Depend on location 
•Local back pain & radicular 
pain 
•Worsening pain on 
recumbency
Signal abnormalities 
CSF capping 
cord/cauda displacement 
•T1 iso/ slightly hypointense 
•T2 hyperintense 
•Contrast enhancement
benign, 
excision, Recurrences are rare 
-Posterior laminectomy 
-unilateral facetectomy 
-open dura 
-Dorsal (visualized), Ventral 
(dissect dentate ligament 
-Cauterize tumor 
-Neurostimulation 
-Dumbbell shaped (resection of 
both nerve roots)
-Surgical removal easy due to 
- absence of bony involvement 
- well-defined spinal epidural 
space 
- lack of venous sinus 
involvement 
-Recurrence 10 % 
- Posterior laminectomy 
- Anterior approaches for purely 
ventral tumors 
-Management of the dural base 
• excision of the dural then graft 
• extensive in situ coagulation
-Role of surgery depends on 
size of the tumor and its 
relationship 
-Gross total en bloc resection 
- Small, well circumscribed within 
the fibrous coverings & easily 
separable from the nerve roots 
-Subtotal 
-Radiation therapy
-First 3 decades of life 
-Most common pediatric 
intramedullary cord tumor 
-60% of occur in the 
cervical 
-20% associated syringes 
-Most are grade I or II 
-Associated NF1 
Intra-medullary 
Astrocytomas Ependymoma 
s 
Hemangioblasto 
ma 
80% 8%
-Most common 
intramedullary tumors in 
adults 
-Male = Female, middle 
age 
-65% have associated 
cysts 
-Associated NF2 
-Cellular ependymoma 
the most common 
-Benign, unencapsulated, 
circumscribed and do not
-Associated with von 
Hippel-Lindau syndrome 
(AD) 
-At any age 
-Associated syringes 
-Benign tumors of 
vascular origin 
-Circumscribed, not 
encapsulated 
-located dorsally or 
dorsolaterally
most 
common dysembryogenic 
lesion, increased fat 
deposition in metabolically 
normal fat cells, subpial 
location. 
The lung 
and breast are the most 
common primary tumor 
sites 
history of radiation
•Nonspecific 
neurological deficit 
can cause abrupt 
deterioration 
(ependymomas) 
and 
dysfunction occur early
Cord enlargement 
Enhancement 
•T1 iso/ slightly hypointense 
•T2 hyperintense 
-uniform contrast enhancement 
-Polar cysts 
-Heterogeneous contrast 
enhancement 
-Irregular margins
•Microsurgical removal is the 
most effective treatment of 
ependymomas & 
hemangioblastomas. 
•For astrocytomas are more 
controversial. 
•Resection should be limited to 
tumor tissue 
•Preservation of neurological 
function rather than complete 
tumor resection is paramount
• Preoperative steroids 
and antibiotics 
• General anesthesia, 
intubated & prone 
• Sensory and motor 
evoked potentials 
monitoring 
• Midline skin, 
subperiosteal bony 
dissection 
• Laminectomy extend 
one segment above 
and below the tumor 
•The facets are 
preserved.
• Strict hemeostasis before the 
dura is opened 
• The dura is opened in the 
midline and tented laterally 
with sutures 
• Operating microscope 
• The arachnoid is opened 
• Cord inspected for surface 
abnormalities ,U/S localize 
tumor 
• midline myelotomy through 
the posterior median septum 
• dorsal midline -- midpoint 
between the dorsal nerve root 
entry zones bilaterally 
• Midline crossing vessels in
• Pia incised sharply with a 
micro knife or scissors 
• myelotomy extend over the 
entire rostrocaudal extent of 
the tumor 
• Spreading the posterior 
columns gently with micro 
forceps 
• Pial traction sutures are 
placed 
• Technique of tumor removal 
is determined by the surgical 
Objective (biopsy , removal) 
• Internal decompression with 
an ultrasonic aspirator or 
laser
Q) WHAT TYPES OF NERVES DO 
NEUROFIBROMAS GENERALLY ARISE 
FROM? 
•Dorsal root 
•Ventral root 
•Both of them
INTRADURAL SPINAL NERVE SHEATH TUMORS 
ARE TOTALLY MALIGNANT ( T ) OR ( F ) 
• False only 2.5 % are malignant
MENINGIOMAS USUALLY ARISE 
FROM WHICH TYPE OF CELLS ? 
•Arachnoid cap cells
………. ARE BENIGN TUMORS OF 
VASCULAR ORIGIN ? 
•Hemangioblastomas
Q) IN RESECTING AN INTRAMEDULLARY SPINAL 
CORD TUMOR, WHAT IS A SURE WAY TO 
RECOGNIZE THE MIDLINE IF THE TUMOR IS 
DEFORMING THE NORMAL SPINAL CORD 
ANATOMY? 
• Midpoint between the dorsal nerve root entry zones 
bilaterally
Q) WHAT IS THE MOST COMMON 
INTRAMEDULLARY SPINAL CORD TUMOR IN 
ADULTS? 
•Ependymoma 
•Meningiomas 
•Astrocytoma 
•Hemangioblastoma
Q) WHAT IS THE MOST COMMON 
INTRAMEDULLARY SPINAL CORD TUMOR IN 
PEDIATRIC ? 
•Ependymoma 
•Meningiomas 
•Astrocytoma 
•Hemangioblastoma
THE END 
THANK YOU

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Spinal cord tumors

  • 1. SPINAL CORD TUMORS BY : DR / AHMED MOHAMMED DEBES NEUROSURGERY RESIDENT AT AHMED MAHER TEACHING HOSPITAL CAIRO, EGYPT. TUESDAY 09/10/2014
  • 2. Spinal Cord Tumors Intra-dural Extra-dural Intra-medullary Extra-medullary
  • 3. Extra-medullary Nerve Sheath Tumors Meningioma schwannomas neurofibromas s Filum Terminale Ependymomas • Gross • Micro • Asso. Neurofibromas • Fusiform • Fibrous tissue + nerve fibers • Neurofibromatosis type I Schwannomas • globoid masses, suspended eccentrically • Antoni-A(elongated cells) Antoni-B(stellate-shaped • schwannomatosis
  • 4. • 4th – 6th decade , male = female •Mostly affect dorsal root most common 30% (cervical) 10% 1%
  • 5. arachnoid cap cells decade , •Mainly , upper cervical spine and foramen magnum •ventral or ventrolateral, may •10% •Do not penetrate the pia
  • 6. decade , •Myxopapillary ependymomas •Cuboidal cells surrounding a vascularized core of hyalinized connective tissue •Benign
  • 7. neural crest, benign, neurosecretory granules dumbbell tumors in pediatric thoracic spine rarely cause mass effect CSF drop metastases, direct penetration of the dural root sleeve
  • 8. •Depend on location •Local back pain & radicular pain •Worsening pain on recumbency
  • 9. Signal abnormalities CSF capping cord/cauda displacement •T1 iso/ slightly hypointense •T2 hyperintense •Contrast enhancement
  • 10. benign, excision, Recurrences are rare -Posterior laminectomy -unilateral facetectomy -open dura -Dorsal (visualized), Ventral (dissect dentate ligament -Cauterize tumor -Neurostimulation -Dumbbell shaped (resection of both nerve roots)
  • 11. -Surgical removal easy due to - absence of bony involvement - well-defined spinal epidural space - lack of venous sinus involvement -Recurrence 10 % - Posterior laminectomy - Anterior approaches for purely ventral tumors -Management of the dural base • excision of the dural then graft • extensive in situ coagulation
  • 12. -Role of surgery depends on size of the tumor and its relationship -Gross total en bloc resection - Small, well circumscribed within the fibrous coverings & easily separable from the nerve roots -Subtotal -Radiation therapy
  • 13. -First 3 decades of life -Most common pediatric intramedullary cord tumor -60% of occur in the cervical -20% associated syringes -Most are grade I or II -Associated NF1 Intra-medullary Astrocytomas Ependymoma s Hemangioblasto ma 80% 8%
  • 14. -Most common intramedullary tumors in adults -Male = Female, middle age -65% have associated cysts -Associated NF2 -Cellular ependymoma the most common -Benign, unencapsulated, circumscribed and do not
  • 15. -Associated with von Hippel-Lindau syndrome (AD) -At any age -Associated syringes -Benign tumors of vascular origin -Circumscribed, not encapsulated -located dorsally or dorsolaterally
  • 16. most common dysembryogenic lesion, increased fat deposition in metabolically normal fat cells, subpial location. The lung and breast are the most common primary tumor sites history of radiation
  • 17. •Nonspecific neurological deficit can cause abrupt deterioration (ependymomas) and dysfunction occur early
  • 18. Cord enlargement Enhancement •T1 iso/ slightly hypointense •T2 hyperintense -uniform contrast enhancement -Polar cysts -Heterogeneous contrast enhancement -Irregular margins
  • 19. •Microsurgical removal is the most effective treatment of ependymomas & hemangioblastomas. •For astrocytomas are more controversial. •Resection should be limited to tumor tissue •Preservation of neurological function rather than complete tumor resection is paramount
  • 20. • Preoperative steroids and antibiotics • General anesthesia, intubated & prone • Sensory and motor evoked potentials monitoring • Midline skin, subperiosteal bony dissection • Laminectomy extend one segment above and below the tumor •The facets are preserved.
  • 21. • Strict hemeostasis before the dura is opened • The dura is opened in the midline and tented laterally with sutures • Operating microscope • The arachnoid is opened • Cord inspected for surface abnormalities ,U/S localize tumor • midline myelotomy through the posterior median septum • dorsal midline -- midpoint between the dorsal nerve root entry zones bilaterally • Midline crossing vessels in
  • 22. • Pia incised sharply with a micro knife or scissors • myelotomy extend over the entire rostrocaudal extent of the tumor • Spreading the posterior columns gently with micro forceps • Pial traction sutures are placed • Technique of tumor removal is determined by the surgical Objective (biopsy , removal) • Internal decompression with an ultrasonic aspirator or laser
  • 23.
  • 24. Q) WHAT TYPES OF NERVES DO NEUROFIBROMAS GENERALLY ARISE FROM? •Dorsal root •Ventral root •Both of them
  • 25. INTRADURAL SPINAL NERVE SHEATH TUMORS ARE TOTALLY MALIGNANT ( T ) OR ( F ) • False only 2.5 % are malignant
  • 26. MENINGIOMAS USUALLY ARISE FROM WHICH TYPE OF CELLS ? •Arachnoid cap cells
  • 27. ………. ARE BENIGN TUMORS OF VASCULAR ORIGIN ? •Hemangioblastomas
  • 28. Q) IN RESECTING AN INTRAMEDULLARY SPINAL CORD TUMOR, WHAT IS A SURE WAY TO RECOGNIZE THE MIDLINE IF THE TUMOR IS DEFORMING THE NORMAL SPINAL CORD ANATOMY? • Midpoint between the dorsal nerve root entry zones bilaterally
  • 29. Q) WHAT IS THE MOST COMMON INTRAMEDULLARY SPINAL CORD TUMOR IN ADULTS? •Ependymoma •Meningiomas •Astrocytoma •Hemangioblastoma
  • 30. Q) WHAT IS THE MOST COMMON INTRAMEDULLARY SPINAL CORD TUMOR IN PEDIATRIC ? •Ependymoma •Meningiomas •Astrocytoma •Hemangioblastoma