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Introduction
 Meningiomas orginate from arachnoid capcells
 SWM : bonycrest formed bywings (lesserand greater) the sphenoid bone.
 sphenoid ridge(lesser wing : internal 2/3 & greater wing its external1/3)
Cont…
Classification by cushings and
eisenhert
 En-plaque/spheno-orbital/hyperostotic
 Globoid meningiomas:
(1) deep, inner, orclinoidal
(2) middle oralar
(3) lateral, outer, orpterional
Enplaque/spheno-
orbital/hyperostotic
 carpet-like duralgrowth
 reactive hyperostosis
 extends :
 posteriorly :cavernoussinus
 anteriorly :orbital apex
Causes of hyperstosis
 vasculardisturbances
 Irritation of bone without actualinvasion
 previous trauma
 bone production by tumorcells
 osteoblastic stimulation of normalbone
 bonegrowth is actually bone invasion by tumorcells.
Location of hyperstosis according
to frequency
 lesser wing of the sphenoidbone
 the greater wing of thesphenoid
 The roof of theorbit
 the inferior orbitalfissure
 the infratemporal fossa
 the orbital rim
GLOBOID MENINGIOMAS
(1) deep, inner, orclinoidal
(2) middle oralar
(3) lateral, outer, orpterional
Pathophysiology
 Head injury
 Radiations
 Harmonal (estrogen & progestrerone)
 Genetic(loss of DNA on 22chromose)
 Androgen receptors(EGF,PDGF)
 Viruses(Inoue-melnick virus)
 Associated(gliomas,abscess & aneurysms)
Epidemiology
 Race( Caucasians, Africans, African Americans,and
Asians)
 Sex(Caucasians:75%women & 25% men.Africansshow
an equal genderratio).
 Age(onset is 50 years increasesthereafter)
 Mortality(5years:87% & 10 years :58%)
Histologic findings
 According to the World Health Organization (WHO)
in 1993, :
 Benign (grade I) : do not invade thebrain
parenchyma.
 Atypical (grade II) : mitosis & increased
nuclear-cytoplasmicratio.
 Malignant (grade III and IV) : greatermitosis,
necrosis, and invasion of brainparenchyma.
Presentation
 Headache
 orbital pain
 visual deficit
 Ptosis
 diplopia
 Ectropion
 Conjunctivitis
Presentation
corneal ulceration,
scleral hemorrhages
Oculomotordeficit
Facial hypoesthesia.
Memory impairment
olfactory hallucinations
hemiparesis.
Differenetial diagnosis
 Fibrousdysplasia
 Osteoma
 osteoblastic metastasis
 Paget’sdisease,
 hyperostosis frontalisinterna
 erythroid hyperplasia
 sarcoidosis
Workup
CT scan and MRI
carotid arteriography
Medical treatment
 Indications:
 atypical and malignant meningiomasas an adjunct to
surgery
 partially resected benign meningiomas
 recurrenceof meningiomasaftera surgical resection.
Medical treatment
 Drugs:
 Antiestrogen(tamoxifen:nolvadex)
 Antiprogestrone(gastrinone)
 Mifepristone, RU-486 (Mifeprex)
 Antineoplastic(hydo-oxyurea & interferonalpha
2B)
 Anti-PDGF(trapidil)
 Dopamineantagonist(bromocriptine)
Surgery
 Indications:
 size of the lesion>2.5cm
 presence of signs orsymptoms
 patient’scondition
 changes in theadjacentcerebral tissue (edema) on
imaging studies
 surgeon’sexperience.
Goal of surgery
 radical excision of thetumor
 resection of the lesion + the dural implant(1-cm
margin) + all hyperostoticbone.
Preparation
 intravenous generalanesthesia.
 Antiepilepticdrugs
 broad-spectrumantibiotics
 Glucocorticoids
 Neurophysiologic monitoring
Positioning
 supine decubitusposition
 the head fixed in a three-pin headholder
 head is slightlyextension
 rotated toward thecontralateral sideof the tumor
 clinoidal tumors (between 30 and40)
 alar and pterional lesions(between 40 and50)
Skin incision
 a frontotemporal(pterional) curvilinear
 starting at the rootof the zygomaticarch, just 5 mm in
front of thetragus
 runs verticallyupward
 Once it passes theear, it is curved rostrallyand
superiorly toward the ipsilateral frontalregion.
Variation in skin incision
 The midportion of incision can be extended backward,
especially in cases of pterional meningiomas with large
infiltration of thepterion.
 If an orbitozygomatic (OZ) approach is required, it is
necessary toextend the incisionverticallydown to the
level of the earlobe.
Dissection of epicranial planes
 superficial temporal artery
 a posterior branch has to be coagulated
 Dissection continues until the temporal fasciais
identified
 Avoid wide separation between the temporalfascia
and the skin to avoid injury to the frontotemporal
branch of the facial nerve
Cont..
 retrograde direction
 two epicranial planes arecreated
 skin and temporal fascia (fasciocutaneousflap)
 temporal muscle alone (muscleflap)
Craniotomy & tumor resection
 anatomic variety of themeningioma
 Pterional
 Alar
 Clinoidal
 En-plaque
Pterional
 If hyperstosis:around the bone infiltration,bone flapof
around 5cm
 If hyperstosis is absent:standardcraniotomy
 Section the tumortoelevate/remove the bone flap
Pterional craniotomy
Alar
 frontotemporal craniotomy
 extradural resection of the lesserwing of the sphenoid
bone.
 Bone removal iscontinued until completeexposureof
the superior orbitalfissure
 The dura mater is then opened following a curvilinear
frontotemporal incision, reflecting the dural flap
forward
clinoidal
 a frontotemporal
 resection of the sphenoidridge
 The superiororbital fissure is alsocompletelyopened
 the posterolateral wall of theorbit is also removed in
case of orbital part oftumor
 Anterior clinoidectomy:high speeddrill+irrigation
Cont..
wide splitting the sylvianfissure
 Retractorsare placed on the frontal and temporal
lobes
Cont..
 dural implants :coagulated
 distal branches of theMCA to
be identified
 distal to proximaldirection
 initial debulking
 Arterial dissection:proximally
 The opticnerve
En-plaque
 it is easier toexpose theentire hyperostosis
 pterional craniotomy is combined with an OZ
osteotomy,particularly when the lesion extends into
the inferiororbital fissure, infratemporal fossa, ororbit
Reconstruction & closure
 resect a free duralmargin
 closure of the dura maternecessarily implies
application of agraft
 Local tissue:aponeurotic galea, pericranium,or
temporal fascia
 Distant tissues fascia:lataorabdominal fascia
 Synthetic & biologic materials, butwith a slightly
higher risk of infection.
 Watertight closure ismandatory
Cont…
 reconstruction of the pterionaldefect:
 Autologous materials:splitcalvarial bonegraftorribs
 synthetic materials:methylmethacrylate and titanium
Complications
 Postoperative EDH:due towidedural detachment
 Csf leak
 Seizures:if grow near epileptogenicareas
 Cosmetic problems:inadequatereconstruction
 Infection:prosthetic material,sinusopened
Results
 In general, the short- and midterm follow-upresults
after SWM resection areexcellent
 In the majorityof 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
inverselyproportional to thedegree of tumorresection
THANK YOU

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Sphenoidwingmeningioma

  • 2. Introduction  Meningiomas orginate from arachnoid capcells  SWM : bonycrest formed bywings (lesserand greater) the sphenoid bone.  sphenoid ridge(lesser wing : internal 2/3 & greater wing its external1/3)
  • 4. Classification by cushings and eisenhert  En-plaque/spheno-orbital/hyperostotic  Globoid meningiomas: (1) deep, inner, orclinoidal (2) middle oralar (3) lateral, outer, orpterional
  • 5. Enplaque/spheno- orbital/hyperostotic  carpet-like duralgrowth  reactive hyperostosis  extends :  posteriorly :cavernoussinus  anteriorly :orbital apex
  • 6. Causes of hyperstosis  vasculardisturbances  Irritation of bone without actualinvasion  previous trauma  bone production by tumorcells  osteoblastic stimulation of normalbone  bonegrowth is actually bone invasion by tumorcells.
  • 7. Location of hyperstosis according to frequency  lesser wing of the sphenoidbone  the greater wing of thesphenoid  The roof of theorbit  the inferior orbitalfissure  the infratemporal fossa  the orbital rim
  • 8. GLOBOID MENINGIOMAS (1) deep, inner, orclinoidal (2) middle oralar (3) lateral, outer, orpterional
  • 9.
  • 10. Pathophysiology  Head injury  Radiations  Harmonal (estrogen & progestrerone)  Genetic(loss of DNA on 22chromose)  Androgen receptors(EGF,PDGF)  Viruses(Inoue-melnick virus)  Associated(gliomas,abscess & aneurysms)
  • 11. Epidemiology  Race( Caucasians, Africans, African Americans,and Asians)  Sex(Caucasians:75%women & 25% men.Africansshow an equal genderratio).  Age(onset is 50 years increasesthereafter)  Mortality(5years:87% & 10 years :58%)
  • 12. Histologic findings  According to the World Health Organization (WHO) in 1993, :  Benign (grade I) : do not invade thebrain parenchyma.  Atypical (grade II) : mitosis & increased nuclear-cytoplasmicratio.  Malignant (grade III and IV) : greatermitosis, necrosis, and invasion of brainparenchyma.
  • 13. Presentation  Headache  orbital pain  visual deficit  Ptosis  diplopia  Ectropion  Conjunctivitis
  • 14. Presentation corneal ulceration, scleral hemorrhages Oculomotordeficit Facial hypoesthesia. Memory impairment olfactory hallucinations hemiparesis.
  • 15. Differenetial diagnosis  Fibrousdysplasia  Osteoma  osteoblastic metastasis  Paget’sdisease,  hyperostosis frontalisinterna  erythroid hyperplasia  sarcoidosis
  • 16. Workup CT scan and MRI carotid arteriography
  • 17. Medical treatment  Indications:  atypical and malignant meningiomasas an adjunct to surgery  partially resected benign meningiomas  recurrenceof meningiomasaftera surgical resection.
  • 18. Medical treatment  Drugs:  Antiestrogen(tamoxifen:nolvadex)  Antiprogestrone(gastrinone)  Mifepristone, RU-486 (Mifeprex)  Antineoplastic(hydo-oxyurea & interferonalpha 2B)  Anti-PDGF(trapidil)  Dopamineantagonist(bromocriptine)
  • 19. Surgery  Indications:  size of the lesion>2.5cm  presence of signs orsymptoms  patient’scondition  changes in theadjacentcerebral tissue (edema) on imaging studies  surgeon’sexperience.
  • 20. Goal of surgery  radical excision of thetumor  resection of the lesion + the dural implant(1-cm margin) + all hyperostoticbone.
  • 21. Preparation  intravenous generalanesthesia.  Antiepilepticdrugs  broad-spectrumantibiotics  Glucocorticoids  Neurophysiologic monitoring
  • 22. Positioning  supine decubitusposition  the head fixed in a three-pin headholder  head is slightlyextension  rotated toward thecontralateral sideof the tumor  clinoidal tumors (between 30 and40)  alar and pterional lesions(between 40 and50)
  • 23. Skin incision  a frontotemporal(pterional) curvilinear  starting at the rootof the zygomaticarch, just 5 mm in front of thetragus  runs verticallyupward  Once it passes theear, it is curved rostrallyand superiorly toward the ipsilateral frontalregion.
  • 24. Variation in skin incision  The midportion of incision can be extended backward, especially in cases of pterional meningiomas with large infiltration of thepterion.  If an orbitozygomatic (OZ) approach is required, it is necessary toextend the incisionverticallydown to the level of the earlobe.
  • 25.
  • 26. Dissection of epicranial planes  superficial temporal artery  a posterior branch has to be coagulated  Dissection continues until the temporal fasciais identified  Avoid wide separation between the temporalfascia and the skin to avoid injury to the frontotemporal branch of the facial nerve
  • 27. Cont..  retrograde direction  two epicranial planes arecreated  skin and temporal fascia (fasciocutaneousflap)  temporal muscle alone (muscleflap)
  • 28. Craniotomy & tumor resection  anatomic variety of themeningioma  Pterional  Alar  Clinoidal  En-plaque
  • 29. Pterional  If hyperstosis:around the bone infiltration,bone flapof around 5cm  If hyperstosis is absent:standardcraniotomy  Section the tumortoelevate/remove the bone flap
  • 31. Alar  frontotemporal craniotomy  extradural resection of the lesserwing of the sphenoid bone.  Bone removal iscontinued until completeexposureof the superior orbitalfissure  The dura mater is then opened following a curvilinear frontotemporal incision, reflecting the dural flap forward
  • 32.
  • 33. clinoidal  a frontotemporal  resection of the sphenoidridge  The superiororbital fissure is alsocompletelyopened  the posterolateral wall of theorbit is also removed in case of orbital part oftumor  Anterior clinoidectomy:high speeddrill+irrigation
  • 34. Cont.. wide splitting the sylvianfissure  Retractorsare placed on the frontal and temporal lobes
  • 35. Cont..  dural implants :coagulated  distal branches of theMCA to be identified  distal to proximaldirection  initial debulking  Arterial dissection:proximally  The opticnerve
  • 36.
  • 37.
  • 38. En-plaque  it is easier toexpose theentire hyperostosis  pterional craniotomy is combined with an OZ osteotomy,particularly when the lesion extends into the inferiororbital fissure, infratemporal fossa, ororbit
  • 39.
  • 40.
  • 41. Reconstruction & closure  resect a free duralmargin  closure of the dura maternecessarily implies application of agraft  Local tissue:aponeurotic galea, pericranium,or temporal fascia  Distant tissues fascia:lataorabdominal fascia  Synthetic & biologic materials, butwith a slightly higher risk of infection.  Watertight closure ismandatory
  • 42. Cont…  reconstruction of the pterionaldefect:  Autologous materials:splitcalvarial bonegraftorribs  synthetic materials:methylmethacrylate and titanium
  • 43. Complications  Postoperative EDH:due towidedural detachment  Csf leak  Seizures:if grow near epileptogenicareas  Cosmetic problems:inadequatereconstruction  Infection:prosthetic material,sinusopened
  • 44. Results  In general, the short- and midterm follow-upresults after SWM resection areexcellent  In the majorityof 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 inverselyproportional to thedegree of tumorresection