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Rahmi Ardhini
Bag/KSM Neurologi FKUNDIP/RSUP dr. Kariadi Semarang
Secondary SCT
Neoplasm that arise as metastatic deposits, within the
spinal cord parenchyma or surrounding tissues, from
a primary lesion outside of the CNS
EPIDEMIOLOGY
• Spinal tumors account for 15% of all CNS tumors
• Incidence 0,5 – 2,5 cases / 100.000 population
• Both genders are equally affected
• 60% extradural, 40% intradural
• Metastatic tumors are most common tumors of the
spine
• 50 – 55% located in thoracal segment
Epidemiology
EXTRADURAL INTRADURAL
Primary
Extramedullary Intramedullary
Hemangioma
Osteoid-osteoma
Osteoblastoma Primary
Osteochondroma Nerve sheath tumor Primary
Giant-cell tumor Meningioma Ependymoma
Chondrosarcoma Fillum terminal Astrocytoma
Ewing’s Sarcoma ependymoma
Multiple myeloma Hemangioblastoma
Paraganglioma
Ganglioneuroma Secondary
Secondary
Spinal Metastasis Intramedullary
Secondary metastasis
Extramedullary
metastasis
Historic classification of spine tumors based on
myelography
(A) Normal,
(B) Extradural
(C) Intradural extramedullary
(D) Intradural intramedullary
SPINAL TUMORS IMAGING METHODS
• Plain Radiograph (X-rays)
• Computed Tomography (CT)
o Conventional CT
o Myelo-CT
• Magnetic Resonance Imaging (MRI)
• Technetium-99m (99mTc) bone scans
• Single photon emission computed tomography
(SPECT)
• Positron Emission Tomography (PET)
• Spinal Angiography
Plain Radiograph
Typical spotted bright signal intensity changes within the vertebral body of L1 on a
T1W and b T2W image suggesting a benign hemangioma
Osteoid Osteoma
(a) T1W showing a round, well demarcated tumor with intense contrast enhance
(b) T2W + C
(c) Axial T1 contrast, showing a typical dumbbell-shape
MENINGIOMA
CT
Low-grade : hypodense, homogeneous with minimal or absent
contrast enhancement
High-grade tumors may show areas of more intense contrast
enhancement and internal heterogenity
MRI
Diffuse astrocytomas : T1W hypointense – isointense ; T2W hyper-
intense
Poorly defined margins
Contrast enhancement is usually mild and may be focal or diffuse or
may be completely absent
Astrocytoma
(A) Sagital T2W and (B) T1W + contrast demonstrate an expanded cord with
heterogenously enhancing tumor with a cystic-necrotic degeneration.
Astrocytoma
HEMANGIOBLASTOMA
Hemangioblastoma. (A) T2W sagital images show a heterogenous mass at T6 associated with cord edema
and hypointensity linear structure consistent with a vessel posterior to the cord. (B) T1W image show
enhancing bilobulated mass. (C) Axial T1W contrast show bilobulated mass and extramedullary “snowman”
appearance. (D) Axial T2W show hyperintensity signal with extensive holocord edema.
INTRAMEDULLARY
METASTASIS