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Meningioma   신경외과 김선환 2001 년  7 월  26 일
General Consideration   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Incidence   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Origin  ,[object Object],[object Object]
Etiology  I ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Etiology  II ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pathology:   Macroscopic features ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pathology:   Macroscopic features
Pathology:   Macroscopic features Hyperostosis of skull Bony erosion
Pathology:   WHO classification(1993) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pathology:  Russell classification   Papillary   Malignant   Hemangioblastic Transitional Hemangiopericytic   Angioblastic   Psammomatous,   Microcystic Myxomatous,   Xanthomatous Lipomatous,   Granular Secretory,   Chondroblastic Osteoblastic,   Melanotic Giant cell,   Lymphoid,   Choroids   Meningothelial Transitional  Fibrous   Classic   Variants   Subtype   Group
Pathology:   Microscopic  features ,[object Object]
Pathology:   Microscopic  features ,[object Object]
Pathology:   Microscopic  features ,[object Object]
Pathology:   Microscopic  features ,[object Object]
Image:  Plain X-ray   ,[object Object],[object Object]
Image: CT ,[object Object],[object Object],[object Object]
Image: CT Pre-enhance CT Post-enhance CT
Image: MRI ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Image: MRI T1-Pre enhance T1-Post enhance T2WI
Image: Cerebral Angiography ,[object Object],[object Object],[object Object],[object Object]
Image: Cerebral Angiography
Location   ,[object Object],[object Object],[object Object],[object Object]
Location
Clinical Manifestation   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Manifestation  by   Specific location Change in mentation,  apathy or disinhibited behavior, urinary incontinence   Subfrontal   Visual Sx, 3 rd  N palsy, Hypopituitarysm, Psychic sx, headache   Tuberculum sellae Headache, seizure, focal weakness   Convexity Ant 1/3: personality change  Mid 1/3: contralateral leg Monoparesis Post 1/3: IICP Sx, visual field defect Parasagittal Symptoms Location
Clinical Manifestation  by   Specific location Symptoms Location Decreased hearing with possible facial weakness and facial numbness   Cerebellopontine angle   Contralateral hemianopsia   Occipital lobe   Multiple cranial N deficits (II, III, IV, V and VI), leading to decreased vision and diplopia with associated to facial numbness   Cavernous sinus   Anosmia with ipsilateral optic atrophy and contralateral papilledema; Kennedy-Foster syndrome.   Olfactory groove
Clinical Manifestation  by   Specific location Symptoms Location Paraparesis; stereoanesthesia, gait disturbance  Foramen magnum  supratentorial and infratentorial; seizure, cerebellar sx, hydrocephalus, visual sx.   Tentorium   Medial 1/3(clinoidal): multiple cranial nerve palsies Middle 1/3(alar): headache, seizure  Lateral 1/3(pterional): seizure, palpable mass  Sphenoid wing  Exophthalmos, Monocular loss of vision; ipsilateral dilated pupil orbital
Management: Surgery   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Management:  Radiation Therapy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Management:  Chemotherapy ,[object Object],[object Object]
Recurrence & Prognosis ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Malignant meningioma ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Multiple meningioma ,[object Object],[object Object],[object Object],[object Object]
Meningioma in children ,[object Object],[object Object],[object Object],[object Object],[object Object]

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Meningioma

  • 1. Meningioma 신경외과 김선환 2001 년 7 월 26 일
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  • 8. Pathology: Macroscopic features
  • 9. Pathology: Macroscopic features Hyperostosis of skull Bony erosion
  • 10.
  • 11. Pathology: Russell classification Papillary Malignant Hemangioblastic Transitional Hemangiopericytic Angioblastic Psammomatous, Microcystic Myxomatous, Xanthomatous Lipomatous, Granular Secretory, Chondroblastic Osteoblastic, Melanotic Giant cell, Lymphoid, Choroids Meningothelial Transitional Fibrous Classic Variants Subtype Group
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  • 18. Image: CT Pre-enhance CT Post-enhance CT
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  • 20. Image: MRI T1-Pre enhance T1-Post enhance T2WI
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  • 26. Clinical Manifestation by Specific location Change in mentation, apathy or disinhibited behavior, urinary incontinence Subfrontal Visual Sx, 3 rd N palsy, Hypopituitarysm, Psychic sx, headache Tuberculum sellae Headache, seizure, focal weakness Convexity Ant 1/3: personality change Mid 1/3: contralateral leg Monoparesis Post 1/3: IICP Sx, visual field defect Parasagittal Symptoms Location
  • 27. Clinical Manifestation by Specific location Symptoms Location Decreased hearing with possible facial weakness and facial numbness Cerebellopontine angle Contralateral hemianopsia Occipital lobe Multiple cranial N deficits (II, III, IV, V and VI), leading to decreased vision and diplopia with associated to facial numbness Cavernous sinus Anosmia with ipsilateral optic atrophy and contralateral papilledema; Kennedy-Foster syndrome. Olfactory groove
  • 28. Clinical Manifestation by Specific location Symptoms Location Paraparesis; stereoanesthesia, gait disturbance Foramen magnum supratentorial and infratentorial; seizure, cerebellar sx, hydrocephalus, visual sx. Tentorium Medial 1/3(clinoidal): multiple cranial nerve palsies Middle 1/3(alar): headache, seizure Lateral 1/3(pterional): seizure, palpable mass Sphenoid wing Exophthalmos, Monocular loss of vision; ipsilateral dilated pupil orbital
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