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BENIGN PRIMARY SPINAL BONY
TUMORS
Dr Sumit Sinha MS, DNB, MNAMS, MCh
Faculty, AO Spine
Faculty, Advanced Trauma Life Support
Fellow, Fujita Health University, Japan
Spine fellow, Pontificial Catholic university, Curitiba, Brazil
Associate Professor
Deptt of Neurosurgery, All India Institute of Medical Sciences
and Associated JPNA Trauma center, New Delhi
SPINAL BONY TUMORS
CELL OF ORIGIN BENIGN MALIGNANT
Osseous Osteoid osteoma
osteoblastoma
osteosarcoma
Cartilagenous Osteochondroma
Enchondroma
Chodroblastoma
Chondromyxoid fibroma
chondrosarcoma
Fibrous fibroma Fibrosarcoma
MFH
Marrow Ewings sarcoma
MM
Lymphoma
Others Hemangioma
Eosinophillic granuloma
ABC
Giant cell tumor
SPINAL BONY TUMORS
3
SPINAL BONY TUMORS
Osteoid osteoma
β€’ Teens, males
β€’ Spine- <10%
β€’ <2 cm
β€’ MC site- L spine- posterior
Elements
SPINAL BONY TUMORS
Osteoid Osteoma (Contd.)
β€’ Backache-
– not relieved by rest
– Worse at night and with recumbency
– relieved by NSAID
β€’ PAINFUL SCOLIOSIS in adoloscents
β€’ Any back pain > 6 weeks in children/ young
adults- Tc Bone scan- increased uptake
SPINAL BONY TUMORS
Osteoid osteoma (Contd.)
β€’ Radiology-
Round/ oval lesion- radiolucent center with
peripheral sclerosis; (< 2 cm diameter)
CT scan shows the nidus (arrowhead) with a
small area of calcification and no perinidal
sclerosis
SPINAL BONY TUMORS
Osteoid osteoma (Contd.)
Histology
β€’ Background of vascularised
connective tissue with
trabeculation
β€’ Surrounding reactive cortical bone
SPINAL BONY TUMORS
Osteoid osteoma (Contd.)- Treatment
β€’ NSAID’s
β€’ Surgical- goal is complete excision
β€’ Curettage/ intralesional excision- 50% recurrence
β€’ Alcohol/ laser/ RF ablation
β€’ RT- residual/ recurrent lesions
SPINAL BONY TUMORS
Osteoblastoma
β€’ 2-3 decade; males>females
β€’ 40% located in spine
β€’ > 2 cm
β€’ Pain- more constant, less severe, not nocturnal
(opposed to osteoid osteomas)- unresponsive to
NSAID’s
β€’ Treatment- complete surgical excision- wide en
bloc
SPINAL BONY TUMORS
Osteoblastoma (Contd.)
β€’ X Ray- Expansile lesion with well circumscribed
margins and homogenous ossification
β€’ CT-
hypoattenuating area with central
calcifications and minimal surrounding
sclerosis.
destructive expansile lesion with osteoid
matrix extending into the spinal canal.
SPINAL BONY TUMORS
MRI
Mass with low signal intensity
Axial contrast-enhanced fat-saturated T1-
weighted MR image shows marked
enhancement of the lesion
SPINAL BONY TUMORS
Bone-forming tumor with
irregular anastomosing trabeculae
(T) lined by regular osteoblasts
and osteoclasts (arrowheads) and
with rich vascularity (*).
Histology
SPINAL BONY TUMORS
Osteochondroma
β€’ 2-3 decade
β€’ 1/3 of all benign bony tumors
β€’ 1-2% located in spine-
– LS (50%)
– TH (30%) posterior elements- spinous process
– CX (20%)
β€’ Pathogenesis- abnormal cartilage growth
SPINAL BONY TUMORS
Osteochondroma- symptoms-
β€’ Frequently asymptomatic
β€’ Painless prominence of bone
β€’ Pain- mild, increases with activity
β€’ Associated with kyphosis and
spondylolisthesis
β€’ Nerve/ spinal compression
SPINAL BONY TUMORS
CT-
Cortical continuity of the
osteochondroma with the C6
posterior arch.
SPINAL BONY TUMORS
Osteochondroma
β€’ MRI-
β€’ RN scan- increased uptake
SPINAL BONY TUMORS
Histology
regular cartilaginous cap (*)
undergoing enchondral
ossification (arrowhead) leading
to medullary bone (m).
SPINAL BONY TUMORS
Osteochondroma
Treatment-
β€’ Asymptomatic- observe
β€’ Surgery- persistant pain/ disability/ X ray
s/o malignancy
β€’ Change into malignant chondrosarcoma
(10% with multiple lesions)
SPINAL BONY TUMORS
Chondroblastoma- Radiology
Sagittal reformatted CT image- lytic lesion
of the L3 vertebral body with sclerotic
margins
SPINAL BONY TUMORS
Chondroblastoma- Radiology
Sagittal T2-weighted MR image,- lesion
(arrowheads) appears isointense relative to
the normal vertebral bodies
Axial contrast-enhanced fat-saturated T1-
weighted MR- marked enhancement
SPINAL BONY TUMORS
Chondroblastoma- Histology
sheets of uniform chondroblasts with
abundant chondroid matrix (*) and some
osteoclast type giant cells (arrowhead).
SPINAL BONY TUMORS
Vertebral hemangioma
β€’ Dysembryogenetic/ hamartomatous
origin
β€’ > middle age
β€’ Slight female predilection
β€’ Site- Th/ L spine.
β€’ usually confined to the vertebral body, occasionally
extend into the posterior elements.
SPINAL BONY TUMORS
Haemangiomas- symptoms
β€’ Mostly asymptomatic.
β€’ Occasionally- increase in size and
compress the spinal cord and nerve roots
SPINAL BONY TUMORS
Radiology
Axial T2-weighted MR image- well-
circumscribed fatty lesion with coarse vertical
trabeculae (polka dots).
Hemangioma of the T9 vertebral body in an
81-year-old woman with multiple osteoporotic
compression fractures (T10–T12).
SPINAL BONY TUMORS
Haemangioma- Histology
thin-walled vessels lined by flat, bland
endothelial cells infiltrating the
medullary cavity between bone
trabeculae
SPINAL BONY TUMORS
Haemangiomas- Treatment
β€’ Transarterial embolization- for painful
intraosseous hemangioma and for reducing
intraoperative blood loss before decompressive
surgery
β€’ Surgery- Rapid tumor growth with spinal cord
compression
SPINAL BONY TUMORS
Fluid levels- heterogenous signal T1/T2
Cystic expansile lytic lesion- thin
cortical shell-
MC site- long bones/ spine-
thoracic vertebrae- posterior
elements
Aneurysmal Bone Cyst
Age- <20 yrs
Females >males
SPINAL BONY TUMORS
Aneurysmal Bone Cyst- histology
β€’ histology
blood-filled cystic spaces separated by
a spindle cell stroma with osteoclast-
like giant cells and osteoid or bone
production
SPINAL BONY TUMORS
Aneurysmal Bone Cyst-Treatment-
β€’ Embolisation only
β€’ Embolisation – surgery
β€’ Complete surgical excision
β€’ RT- for residual/ recurrent tumors
SPINAL BONY TUMORS
Giant cell tumors-
β€’ 2-4th decade
β€’ Females common
β€’ Sacrum (MC Site)- upper part/ wing>L>Th>Cx
β€’ Intervertebral disk invasion and extension into an
adjacent vertebra
SPINAL BONY TUMORS
well-defined lytic lesion of the right
upper part of the sacrum with
extension through the right sacroiliac
joint and absence of a sclerotic rim.
SPINAL BONY TUMORS
Giant cell tumors-
β€’ Histology
osteoclast type giant cells with
numerous nuclei (*) scattered among
regular mononuclear cells.
SPINAL BONY TUMORS
Langerhans cell histiocytosis (histiocytosis X)-
β€’ eosinophilic granuloma- usually solitary and
curable
β€’ SchΓΌller-Christian syndrome- Disseminated
process
β€’ Letterer-Siwe disease- Rapidly fatal
β€’ 5 and 10 years
β€’ Vertebral involvement- 7.8%–25%
SPINAL BONY TUMORS
Radiology
Eosinophilic granuloma in a 12-year-old
boy. Radiograph shows increased opacity in
an incompletely collapsed vertebral body
SPINAL BONY TUMORS
Treatment
β€’ Controversial.
β€’ Conservative- Patients without complications
β€’ In patients with multifocal disorders- biopsy of
extraspinal lesions and chemotherapy

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Benign primary spinal bony tumors

  • 1. BENIGN PRIMARY SPINAL BONY TUMORS Dr Sumit Sinha MS, DNB, MNAMS, MCh Faculty, AO Spine Faculty, Advanced Trauma Life Support Fellow, Fujita Health University, Japan Spine fellow, Pontificial Catholic university, Curitiba, Brazil Associate Professor Deptt of Neurosurgery, All India Institute of Medical Sciences and Associated JPNA Trauma center, New Delhi
  • 2. SPINAL BONY TUMORS CELL OF ORIGIN BENIGN MALIGNANT Osseous Osteoid osteoma osteoblastoma osteosarcoma Cartilagenous Osteochondroma Enchondroma Chodroblastoma Chondromyxoid fibroma chondrosarcoma Fibrous fibroma Fibrosarcoma MFH Marrow Ewings sarcoma MM Lymphoma Others Hemangioma Eosinophillic granuloma ABC Giant cell tumor
  • 4. SPINAL BONY TUMORS Osteoid osteoma β€’ Teens, males β€’ Spine- <10% β€’ <2 cm β€’ MC site- L spine- posterior Elements
  • 5. SPINAL BONY TUMORS Osteoid Osteoma (Contd.) β€’ Backache- – not relieved by rest – Worse at night and with recumbency – relieved by NSAID β€’ PAINFUL SCOLIOSIS in adoloscents β€’ Any back pain > 6 weeks in children/ young adults- Tc Bone scan- increased uptake
  • 6. SPINAL BONY TUMORS Osteoid osteoma (Contd.) β€’ Radiology- Round/ oval lesion- radiolucent center with peripheral sclerosis; (< 2 cm diameter) CT scan shows the nidus (arrowhead) with a small area of calcification and no perinidal sclerosis
  • 7. SPINAL BONY TUMORS Osteoid osteoma (Contd.) Histology β€’ Background of vascularised connective tissue with trabeculation β€’ Surrounding reactive cortical bone
  • 8. SPINAL BONY TUMORS Osteoid osteoma (Contd.)- Treatment β€’ NSAID’s β€’ Surgical- goal is complete excision β€’ Curettage/ intralesional excision- 50% recurrence β€’ Alcohol/ laser/ RF ablation β€’ RT- residual/ recurrent lesions
  • 9. SPINAL BONY TUMORS Osteoblastoma β€’ 2-3 decade; males>females β€’ 40% located in spine β€’ > 2 cm β€’ Pain- more constant, less severe, not nocturnal (opposed to osteoid osteomas)- unresponsive to NSAID’s β€’ Treatment- complete surgical excision- wide en bloc
  • 10. SPINAL BONY TUMORS Osteoblastoma (Contd.) β€’ X Ray- Expansile lesion with well circumscribed margins and homogenous ossification β€’ CT- hypoattenuating area with central calcifications and minimal surrounding sclerosis. destructive expansile lesion with osteoid matrix extending into the spinal canal.
  • 11. SPINAL BONY TUMORS MRI Mass with low signal intensity Axial contrast-enhanced fat-saturated T1- weighted MR image shows marked enhancement of the lesion
  • 12. SPINAL BONY TUMORS Bone-forming tumor with irregular anastomosing trabeculae (T) lined by regular osteoblasts and osteoclasts (arrowheads) and with rich vascularity (*). Histology
  • 13. SPINAL BONY TUMORS Osteochondroma β€’ 2-3 decade β€’ 1/3 of all benign bony tumors β€’ 1-2% located in spine- – LS (50%) – TH (30%) posterior elements- spinous process – CX (20%) β€’ Pathogenesis- abnormal cartilage growth
  • 14. SPINAL BONY TUMORS Osteochondroma- symptoms- β€’ Frequently asymptomatic β€’ Painless prominence of bone β€’ Pain- mild, increases with activity β€’ Associated with kyphosis and spondylolisthesis β€’ Nerve/ spinal compression
  • 15. SPINAL BONY TUMORS CT- Cortical continuity of the osteochondroma with the C6 posterior arch.
  • 16. SPINAL BONY TUMORS Osteochondroma β€’ MRI- β€’ RN scan- increased uptake
  • 17. SPINAL BONY TUMORS Histology regular cartilaginous cap (*) undergoing enchondral ossification (arrowhead) leading to medullary bone (m).
  • 18. SPINAL BONY TUMORS Osteochondroma Treatment- β€’ Asymptomatic- observe β€’ Surgery- persistant pain/ disability/ X ray s/o malignancy β€’ Change into malignant chondrosarcoma (10% with multiple lesions)
  • 19. SPINAL BONY TUMORS Chondroblastoma- Radiology Sagittal reformatted CT image- lytic lesion of the L3 vertebral body with sclerotic margins
  • 20. SPINAL BONY TUMORS Chondroblastoma- Radiology Sagittal T2-weighted MR image,- lesion (arrowheads) appears isointense relative to the normal vertebral bodies Axial contrast-enhanced fat-saturated T1- weighted MR- marked enhancement
  • 21. SPINAL BONY TUMORS Chondroblastoma- Histology sheets of uniform chondroblasts with abundant chondroid matrix (*) and some osteoclast type giant cells (arrowhead).
  • 22. SPINAL BONY TUMORS Vertebral hemangioma β€’ Dysembryogenetic/ hamartomatous origin β€’ > middle age β€’ Slight female predilection β€’ Site- Th/ L spine. β€’ usually confined to the vertebral body, occasionally extend into the posterior elements.
  • 23. SPINAL BONY TUMORS Haemangiomas- symptoms β€’ Mostly asymptomatic. β€’ Occasionally- increase in size and compress the spinal cord and nerve roots
  • 24. SPINAL BONY TUMORS Radiology Axial T2-weighted MR image- well- circumscribed fatty lesion with coarse vertical trabeculae (polka dots). Hemangioma of the T9 vertebral body in an 81-year-old woman with multiple osteoporotic compression fractures (T10–T12).
  • 25. SPINAL BONY TUMORS Haemangioma- Histology thin-walled vessels lined by flat, bland endothelial cells infiltrating the medullary cavity between bone trabeculae
  • 26. SPINAL BONY TUMORS Haemangiomas- Treatment β€’ Transarterial embolization- for painful intraosseous hemangioma and for reducing intraoperative blood loss before decompressive surgery β€’ Surgery- Rapid tumor growth with spinal cord compression
  • 27. SPINAL BONY TUMORS Fluid levels- heterogenous signal T1/T2 Cystic expansile lytic lesion- thin cortical shell- MC site- long bones/ spine- thoracic vertebrae- posterior elements Aneurysmal Bone Cyst Age- <20 yrs Females >males
  • 28. SPINAL BONY TUMORS Aneurysmal Bone Cyst- histology β€’ histology blood-filled cystic spaces separated by a spindle cell stroma with osteoclast- like giant cells and osteoid or bone production
  • 29. SPINAL BONY TUMORS Aneurysmal Bone Cyst-Treatment- β€’ Embolisation only β€’ Embolisation – surgery β€’ Complete surgical excision β€’ RT- for residual/ recurrent tumors
  • 30. SPINAL BONY TUMORS Giant cell tumors- β€’ 2-4th decade β€’ Females common β€’ Sacrum (MC Site)- upper part/ wing>L>Th>Cx β€’ Intervertebral disk invasion and extension into an adjacent vertebra
  • 31. SPINAL BONY TUMORS well-defined lytic lesion of the right upper part of the sacrum with extension through the right sacroiliac joint and absence of a sclerotic rim.
  • 32. SPINAL BONY TUMORS Giant cell tumors- β€’ Histology osteoclast type giant cells with numerous nuclei (*) scattered among regular mononuclear cells.
  • 33. SPINAL BONY TUMORS Langerhans cell histiocytosis (histiocytosis X)- β€’ eosinophilic granuloma- usually solitary and curable β€’ SchΓΌller-Christian syndrome- Disseminated process β€’ Letterer-Siwe disease- Rapidly fatal β€’ 5 and 10 years β€’ Vertebral involvement- 7.8%–25%
  • 34. SPINAL BONY TUMORS Radiology Eosinophilic granuloma in a 12-year-old boy. Radiograph shows increased opacity in an incompletely collapsed vertebral body
  • 35. SPINAL BONY TUMORS Treatment β€’ Controversial. β€’ Conservative- Patients without complications β€’ In patients with multifocal disorders- biopsy of extraspinal lesions and chemotherapy