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Surgical Management of
Sphenoid Wing Meningiomas
Schmidek Chapter 36
GERARDO GUINTO
Outline
• Anatomy
• Classification
• Clinical course
• Diagnosis
• Treatment
• Complication and result
Anatomy
Classification
En-plaque meningiomas
• Spheno-orbital meningiomas or hyperostotic
meningiomas of the sphenoid wing
• Carpet-like dural growth tumor
• It frequently extends posteriorly toward the cavernous
sinus and anteriorly toward the orbital apex, where it
causes proptosis and oculomotor deficits growth tumor
Globoid meningiomas
• Deep, inner, or clinoidal
– Most common
– Subtype : tumors without extradural growth and tumors
with extradural growth into the cavernous sinus
• Middle
• Lateral, outer, or pterional
Clinical course
• Most common : Protosis which usually is slowly
evolving, unilateral, nonpulsatile, and irreducible
• Protosis Ddx
– Hyperostosis of the orbital walls
– Periorbital tumor invasion
– Intraorbital tumor
– Venous stasis caused by compression of the
ophthalmic veins
Clinical course
• Related symptoms : headache, orbital pain, visual
deficit, ptosis, diplopia, ectropion, conjunctivitis,
corneal ulceration, and scleral hemorrhages
• Clinoidal meningioma
– Visual field problems
– When tumor invade cavernous sinus, the most common
symptoms are oculomotor deficit (especially on cranial
nerve VI) and facial hypoesthesia
Clinical course
• Middle or alar meningiomas
– Late symptoms
– Headache and signs or symptoms suggesting increased
intracranial pressure, such as nausea, vomiting, and
papilledema
• Not common
– Memory impairment
– Olfactory hallucinations
– Personality changes
– Seizures
– Hemiparesis
Diagnosis
• CT
• MRI
• Angiography
Computed tomography
• The extent of bone invasion
• The dural component of these tumors is typically found
as an isodense image with contrast enhancement
• The most common locations of hyperostosis of en-
plaque meningiomas
– the lesser wing of the sphenoid bone
– the greater wing of the sphenoid
– the roof of the orbit
– the inferior orbital fissure
– the infratemporal fossa
– the orbital rim.
Computed tomography
• Globoid tumors : well-defined isodense lesions that
present an intense and homogeneous contrast
enhancement
• Clinoidal meningiomas : hyperostosis of the anterior
clinoid process (ACP), causing narrowing of the optic
canal and the superior orbital fissure
MRI
• Globoid meningiomas show different appearances on
MRI
– When their vascularity is not so marked, they usually
present as a homogeneous isointense lesion in both T1-
and T2-weighted images
– When they are highly vascularized (angioblastic
meningiomas), multiple hypointense images (“empty
signals”) can be seen in the interior of the tumor
MRI
• Gadolinium enhancement is usually intense and uniform
• T2-weighted image is particularly useful in demonstrating
perilesional edema
• Functional MRI
• MRA
Angiography
• Selective catheterization provides specific information
about the blood supply of the tumorand allows the
possibility of preoperative embolization
Treatment
• Indication
– all patients who are in good health and have a tumor size
greater than 2.5 cm
– presence of signs or symptoms
– changes in the adjacent cerebral(edema)
• Objective
– radical excision of the tumor, which means resection of the
lesion, along with the dural implant (1-cm margin) and all
hyperostotic bone
Treatment
• Preparation : general anesthesia, antiepileptic drugs, broad-
spectrum antibiotics, neurophysiologic monitoring
• Positioning and Incision
• Preserve : superficial temporal artery, frontotemporal branch
of facial nerve
•
Pterional
• Pterional craniotomy
• Hyperostosis is usually seen immediately in the
pterion once the temporal muscle is detached :
craniotomy about 5 cms from lesion
• Resection of hyperostosis : 1 cm from margin
• The meningeal portion of the tumor : 1 cm from margin
• In some cases of predominantly osseous tumors :
craniectomy
Pterional
Alar or middle
• Frontotemporal craniotomy
• Extradural resection of the lesser wing of the sphenoid
bone
• Bone removal is continued until complete exposure of the
superior orbital fissure and base of the ACP
• Dura open in curvilinear frontotemporal incision
• Splitting of the sylvian fissure is done
• “En bloc” resection is only possible in small tumors
• Debulking is preferred in the majority of these cases
• Leaving deeper portions and dural implant for the end of the
procedure.
Clinoidal
• Frontotemporal craniotomy
• Bone resection of the sphenoid ridge from the pterion to
the base of the ACP
• If there is an orbital component of the tumor, the
posterolateral wall of the orbit is also removed
• Anterior clinoidectomy : holding the ACP with a rongeur
and applying a gentle “wiggle and jiggle” movement of
the surgeon’s wrist
• The curvilinear dural incision is done
• Splitting of the sylvian fissure is done
Clinoidal
• Initially, the dural implants in the frontal and temporal
regions are coagulated, which reduces vascular
supply of the tumor and facilitates its resection
• Dissection of the tumor
• The optic nerve is next referred intradurally and released
from the tumor
• Extirpation of the dural implant is done
En Plaque
• Pterional craniotomy is combined with an OZ osteotomy
when the lesion extends into the inferior orbital fissure,
infratemporal fossa or orbit
• It is easy to observe the totality of the hyperostosis from
a lateral perspective and the drilling begins
• All infiltrated dura are resected, attempting to extend
this resection beyond the area of dural enhancement
seen on imaging studies.
En Plaque
Reconstruction and closure
• Closure of the dura
– Local tissue : aponeurotic galea, pericranium, or temporal
fascia
– Distant tissue : fascia lata or abdominal fascia
• Reconstruction of the pterional defect
– Autologous materials : split calvarial bone graft or ribs
– Synthetic materials : methylmethacrylate and titanium
Reconstruction and closure
• The floor, the orbital rim or both are removed, all
authors agree that reconstruction is required due to
the high risk of orbital ptosis, postoperative diplopia, or
cosmetic defect
• Reconstruction of the orbital walls is controversial : the
superior and lateral walls of the orbit
Complication
• Postoperative hematoma, especially epidural, due to the
wide dural detachment done in some cases and the
spaces created by resection of large bone formations
• CSF leakage due to wide resection of the dural implant
• Seizure
• Cosmetic
• Infection : when prosthetic materials are used for
reconstruction or when frontal ethmoid or sphenoid
sinuses are inadvertently opened
Result
• The short and midterm follow-up results after SWM
resection are excellent
• In the majority of cases,gross total resection is
accomplished with minimal morbidity
• However, the critical point is in long-term follow-up
because of the high risk of recurrence, which is inversely
proportional to the degree of tumor resection
• Factors : incomplete resection of these tumors are
extent of bone invasion, underevaluation of the dural
component, and invasion of adjacent neurovascular
structures, anaplasia

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Sch.36 surgical management of sphenoid wing meningioma

  • 1. Surgical Management of Sphenoid Wing Meningiomas Schmidek Chapter 36 GERARDO GUINTO
  • 2. Outline • Anatomy • Classification • Clinical course • Diagnosis • Treatment • Complication and result
  • 5. En-plaque meningiomas • Spheno-orbital meningiomas or hyperostotic meningiomas of the sphenoid wing • Carpet-like dural growth tumor • It frequently extends posteriorly toward the cavernous sinus and anteriorly toward the orbital apex, where it causes proptosis and oculomotor deficits growth tumor
  • 6. Globoid meningiomas • Deep, inner, or clinoidal – Most common – Subtype : tumors without extradural growth and tumors with extradural growth into the cavernous sinus • Middle • Lateral, outer, or pterional
  • 7. Clinical course • Most common : Protosis which usually is slowly evolving, unilateral, nonpulsatile, and irreducible • Protosis Ddx – Hyperostosis of the orbital walls – Periorbital tumor invasion – Intraorbital tumor – Venous stasis caused by compression of the ophthalmic veins
  • 8. Clinical course • Related symptoms : headache, orbital pain, visual deficit, ptosis, diplopia, ectropion, conjunctivitis, corneal ulceration, and scleral hemorrhages • Clinoidal meningioma – Visual field problems – When tumor invade cavernous sinus, the most common symptoms are oculomotor deficit (especially on cranial nerve VI) and facial hypoesthesia
  • 9. Clinical course • Middle or alar meningiomas – Late symptoms – Headache and signs or symptoms suggesting increased intracranial pressure, such as nausea, vomiting, and papilledema • Not common – Memory impairment – Olfactory hallucinations – Personality changes – Seizures – Hemiparesis
  • 11. Computed tomography • The extent of bone invasion • The dural component of these tumors is typically found as an isodense image with contrast enhancement • The most common locations of hyperostosis of en- plaque meningiomas – the lesser wing of the sphenoid bone – the greater wing of the sphenoid – the roof of the orbit – the inferior orbital fissure – the infratemporal fossa – the orbital rim.
  • 12. Computed tomography • Globoid tumors : well-defined isodense lesions that present an intense and homogeneous contrast enhancement • Clinoidal meningiomas : hyperostosis of the anterior clinoid process (ACP), causing narrowing of the optic canal and the superior orbital fissure
  • 13. MRI • Globoid meningiomas show different appearances on MRI – When their vascularity is not so marked, they usually present as a homogeneous isointense lesion in both T1- and T2-weighted images – When they are highly vascularized (angioblastic meningiomas), multiple hypointense images (“empty signals”) can be seen in the interior of the tumor
  • 14. MRI • Gadolinium enhancement is usually intense and uniform • T2-weighted image is particularly useful in demonstrating perilesional edema • Functional MRI • MRA
  • 15. Angiography • Selective catheterization provides specific information about the blood supply of the tumorand allows the possibility of preoperative embolization
  • 16. Treatment • Indication – all patients who are in good health and have a tumor size greater than 2.5 cm – presence of signs or symptoms – changes in the adjacent cerebral(edema) • Objective – radical excision of the tumor, which means resection of the lesion, along with the dural implant (1-cm margin) and all hyperostotic bone
  • 17. Treatment • Preparation : general anesthesia, antiepileptic drugs, broad- spectrum antibiotics, neurophysiologic monitoring • Positioning and Incision • Preserve : superficial temporal artery, frontotemporal branch of facial nerve •
  • 18. Pterional • Pterional craniotomy • Hyperostosis is usually seen immediately in the pterion once the temporal muscle is detached : craniotomy about 5 cms from lesion • Resection of hyperostosis : 1 cm from margin • The meningeal portion of the tumor : 1 cm from margin • In some cases of predominantly osseous tumors : craniectomy
  • 20. Alar or middle • Frontotemporal craniotomy • Extradural resection of the lesser wing of the sphenoid bone • Bone removal is continued until complete exposure of the superior orbital fissure and base of the ACP • Dura open in curvilinear frontotemporal incision • Splitting of the sylvian fissure is done • “En bloc” resection is only possible in small tumors • Debulking is preferred in the majority of these cases • Leaving deeper portions and dural implant for the end of the procedure.
  • 21. Clinoidal • Frontotemporal craniotomy • Bone resection of the sphenoid ridge from the pterion to the base of the ACP • If there is an orbital component of the tumor, the posterolateral wall of the orbit is also removed • Anterior clinoidectomy : holding the ACP with a rongeur and applying a gentle “wiggle and jiggle” movement of the surgeon’s wrist • The curvilinear dural incision is done • Splitting of the sylvian fissure is done
  • 22. Clinoidal • Initially, the dural implants in the frontal and temporal regions are coagulated, which reduces vascular supply of the tumor and facilitates its resection • Dissection of the tumor • The optic nerve is next referred intradurally and released from the tumor • Extirpation of the dural implant is done
  • 23.
  • 24. En Plaque • Pterional craniotomy is combined with an OZ osteotomy when the lesion extends into the inferior orbital fissure, infratemporal fossa or orbit • It is easy to observe the totality of the hyperostosis from a lateral perspective and the drilling begins • All infiltrated dura are resected, attempting to extend this resection beyond the area of dural enhancement seen on imaging studies.
  • 26. Reconstruction and closure • Closure of the dura – Local tissue : aponeurotic galea, pericranium, or temporal fascia – Distant tissue : fascia lata or abdominal fascia • Reconstruction of the pterional defect – Autologous materials : split calvarial bone graft or ribs – Synthetic materials : methylmethacrylate and titanium
  • 27. Reconstruction and closure • The floor, the orbital rim or both are removed, all authors agree that reconstruction is required due to the high risk of orbital ptosis, postoperative diplopia, or cosmetic defect • Reconstruction of the orbital walls is controversial : the superior and lateral walls of the orbit
  • 28. Complication • Postoperative hematoma, especially epidural, due to the wide dural detachment done in some cases and the spaces created by resection of large bone formations • CSF leakage due to wide resection of the dural implant • Seizure • Cosmetic • Infection : when prosthetic materials are used for reconstruction or when frontal ethmoid or sphenoid sinuses are inadvertently opened
  • 29. Result • The short and midterm follow-up results after SWM resection are excellent • In the majority of cases,gross total resection is accomplished with minimal morbidity • However, the critical point is in long-term follow-up because of the high risk of recurrence, which is inversely proportional to the degree of tumor resection • Factors : incomplete resection of these tumors are extent of bone invasion, underevaluation of the dural component, and invasion of adjacent neurovascular structures, anaplasia