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Published byMaurice Gilmore Modified over 9 years ago
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Khaled M F SAOUD Professor of neurosurgery, Ain shams university
Spinal Tumors Khaled M F SAOUD Professor of neurosurgery, Ain shams university
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Collaboration
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Diagnosis and Management
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Epidemiology 15% of primary CNS tumors are intraspinal
Intracranial: intraspinal ratio of astrocytoma is 10 :1, and for ependymomas 3-20 :1. Most of primary CNS Spinal tumors are benign!!.
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Anatomical Classification of Spinal Cord Tumors
Extradural : Benign and malignant verteberal tumors, tumors near the spinal cord. Intradural tumors Extramedullary: nerve sheath and menengial Intramedullary: glial and other
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Intra-dural Lesions
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Meningioma Slow growing benign masses
~15% of all meningiomas are spinal 5:1 female to male ratio Typically intradural extramedullary but can be extadural Most commonly thoracic in location, Cervical second most common
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Schwannomas
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Neurofibromas and Neurofibromatosis
Commonly seen in NF-1 Occur more frequently in the cervical spine in NF-1 May be intradural, extradural or dumbell Often multiple Sometimes plexiform Benign Fusiform expansion of the nerve (Schwann, perineural and neural cells) Difficult to get complete resection because of the extra-foramenal extension and risk of functional loss
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Ependymomas Seen in adults, 15 to 40 Male = Female
Presenting signs depend on location Longer duration, more severe symptoms = less favorable functional outcome with surgery Arise from ependymal lining of the central canal & from filum terminale Sometimes associated with a syrinx Filum origin usually myxopapillary type Very rarely malignant Total resection is possible in the majority of tumors The goal of surgery is complete resection with good functional outcome Functional improvement common after resection Progression free survival similar for total resection vs partial resection + RT
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Conus and filum terminale
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Astrocytoma Occur at any age, average age of dx is 35 to 40
Accompanying syrinx in 40% Occurs equally throughout cord Presenting sign depend upon location Most are grade I or II Complete surgical resection is impossible RT recommended after dx Outcomes similar for biopsy + RT and resection + RT Low grade recurrent tumor can be treated with reresection
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Spinal radiosurgery?
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Hemangioblastoma Highly vascular tumors comprising 2% of spinal cord tumors ¼ associated with von Hippel-Lindau, ¾ sporadic 10 times less common than intracranial Male predominance Presents mid life Spinal Angiography?
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Cavernous Angioma Often dorsally located and comes to surface
Hemosiderin stained Resection with second hemorrhage or progressive deficit Thin walled abnormal vascular channels Spinal radiosurgery??
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Lipoma Typically associated with spinal dysrahpism
Presents like any space occupying lesion with progressive myelopathy Onset of symptoms often associated with weight gain Treatment is surgical with debulking of the tumor and duraplasty Must take care not to injure normal spinal cord.
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Spinal metastasis Theatrically can happen anywhere in the spine, ED,ID EM Treatment depends on the symptoms.
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Primary Skeletal Neoplasms
Cell of origin Osseous Cartilagenous Fibrous Benign Malignant Neoplasms Neoplasms Osteoid osteoma Osteosarcoma Osteoblastoma ( and variants Osteochondroma Enchondroma Chondroblastoma Chondromyxoid- fibroma Chondrosarcoma Primary, secondary Fibrosarcoma Malignant fibrous Histiocytoma Fibroma
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Vertebral hemangioma Most common benign spinal neoplasm.
More in the thoracic and lumber spine. Mostly asymptomatic. May present with pain or rarely neurological deficit.
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Vertebral hemangiomas
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Spinal radiosurgery Why? Indications Post resection local irradiation
Disease progression despite previous surgery and/or irradiation Patients with severe medical comorbidities that preclude surgery Inoperable lesions
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Components Immobilization device Radiation unit Beam shaping unit
Respiratory tracking unit
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Respiratory tracking
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Cyber Knife (Frameless SRS):
Real-time X-ray imaging to establish the position of the lesion during treatment The patient wears a vest that contains LED external Fiducials.
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Objectives of spinal RS in spinal mets:
Pain relief (up to 90%) Control of progression (80-90%) –lung and breast best prognosis
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Combined kyphoplasty and spinal radiosurgery for spinal mets COMPRESSION FRACTURES
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Spinal arteriovenous malformations
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Indications Comorbidities Residual/recurrent tumors
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Teamwork Clinical Oncology Neurology Professor Dr Khaled Abdelkarim
Professor Dr Mohamed Sabry AlKady Professor Dr Mohamed Yassin Mostafa Neurology Professor Dr Ahmed AbdelMenem Gaber
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