Tumors of Bone
By Dr SHAHID MANZUR
AAAOCIATE PROFESSOR
Department of Diagnostic Radiology
QAMC / BVH
Intro
 Bone tumors are very diverse in morphology and
biological potential (can be no big deal or rapidly fatal)
 MOST bone tumors are benign lesions
 Most benign lesions are seen <30 years of age
 A new bone tumor in the elderly is more likely to be
malignant
 No bone is safe (though most primaries are in long
bones)
 Locale in the bone gives important Dx info
 More common benign lesions typically present as
incidental findings (non-painful, stable size)
 Be cautious with painful lesions and those that grow
relatively fast (over weeks or months)
 Pathological fracture can be the first sign of tumor
 Bone neoplasms are very difficult to diagnose
specifically on radiologic testing alone
 So why is radiology important?
 Exact location of lesion
 Extent of growth/metastasis
 Aggressiveness
 Best test for Dx= X-ray
 Best test for staging= CT or MRI
 Quick shout out to the pathologists– histologic
grade is the most important prognostic feature
of bone sarcomas and essential for staging most
of the bone tumor types.
Cases
Find the lesion
Example:
Cases
Find the lesion
Example:
RIGHT THERE!
Case I
 16 yr old white male with pain in his left upper
arm.
 Mild swelling and tenderness
 Pain progressively getting worse for ~ 3 months
 Recent onset of mild fever
Imaging:
Imaging:
**
bone tumor 1.ppt
Biopsy material showed a highly cellular, infiltrative neoplasm consisting of
sheets of tightly packed, round cells with very scant cytoplasm ("round blue
cell tumor"). Occasional Homer-Wright rosettes were identified. Other
fields showed extensive necrosis.
bone tumor 1.ppt
bone tumor 1.ppt
bone tumor 1.ppt
Dx: Ewing’s Sarcoma (or PNET)
 #2 primary bone malignancy in kids (5-15 is
most common age group
 Much more common in Caucasians
 Typically in the diaphysis of long tubular bones
or in large flat bone
 Lytic tumor w/ permeative margins extending
into the soft tissue
 Periostial rxn creates sheets of reactive bone in
an onion-skin fashion
Another most excellent
example of “onion-
skinning”
Case II
 33 yr old black female with sudden severe hand
pain after very minor trauma.
 Completely healthy otherwise.
 All labs normal
bone tumor 1.ppt
bone tumor 1.ppt
Dx: Enchondroma
 Benign cartilagenous tumors but hard to
distinguish from a low grade chondrosarcoma
 Acral bones-- the most common primary hand
tumor
 Usually solitary, usually incidental finding (non-
painful unless associated with fracture)
 Get hand films and look for dec. lucency but not
so much as a cyst (more ground-glass) w/ or
w/o areas of stippled calcifications or rings
For boards and wards:
 Multiple enchondromas = ____________
 Multiple enchondromas + hemanigiomas of soft
tissue = _____________
For boards and wards:
 Multiple enchondromas = Ollier’s Dz
 Multiple enchondromas + hemangiomas of soft
tissue = Maffucci syndrome
Case III
 50 yr old white male with back pain
 Mainly lower spine/sacral pain, progressive ~ 8
months
 New onset rectal pain and constipation
bone tumor 1.ppt
bone tumor 1.ppt
CT guided FNA confirmed…
Dx: Chordoma
 Arises from notochord remnants. Thus is
typically midline along the spine and usually at
the ends (Sacrococc or occ/cervical jxn)
 Males>Females, middle age
 + staining w/ S-100 and epithelial markers
 Locally invasive until very late in disease where
mets can go to the lungs, LN, skin.
Case IV
 21 yr old male with new onset chest pain today,
worse on inhalation.
 ROS significant for an ongoing aching leg pain for
the past 6 months which he has put off seeing a
doctor for.
bone tumor 1.ppt
bone tumor 1.ppt
bone tumor 1.ppt
bone tumor 1.ppt
Dx: The dreaded Osteosarcoma
 #1 primary bone malignancy
 Associated with RB1 and p53 gene mutations
 1000x greater risk w/ Hx of hereditary retinoblastoma
 Member of the Li-Fraumeni Syndrome family
 Bimodal age spike: young and elderly
 75% <age 20
 Osteosarcoma in elderly usually from predisposing
mechanism (secondary)
 Paget Dz, bone infarcts, history of radiation, etc
Most patients die from pulmonary complications
after metastatic seeding of the lungs (ex:
pneumothorax)
 Metaphysial tumor
 60% at the knee (distal femur or prox tibia)
 Radiographic terms to know:
 Codman’s Triangle:
 “Sunburst” periostial formation:
 AKA “Hair on end”
For the future Surgeons:
 Rotationplasty is a new solution to disfiguring
surgical resections of lower limb sarcomas:
Quick Hits:
Gout
Incidental
finding on
knee xray
Fabella = posterior sesmoids or
little confused knee caps
13 yr old boy
with superior
tibial pain,
r/o
neoplasm w/
xray shows:
Osgood Schlatter
Metastatic Disease
 Most common malignant lesion of bone
 Bone is # 3 on the list of favorite places for mobile
cancers to go
 Malignant lesions are more likely to be in axial bones
 Typically multifocal BUT renal and thyroid carcinomas
are notorious for producing only a solitary lesion
 Can be lytic, blastic, or both:
 Lung is Lytic, Prostate Produces, Breast does Both
Mets (cont)
 Adults
 Lung
 Prostate
 Breast
 Kidney
 Kids
 NB
 Wilm’s
 OS
 Ewing’s
 Rhabdomyosarcoma
Thanks

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bone tumor 1.ppt

  • 1. Tumors of Bone By Dr SHAHID MANZUR AAAOCIATE PROFESSOR Department of Diagnostic Radiology QAMC / BVH
  • 2. Intro  Bone tumors are very diverse in morphology and biological potential (can be no big deal or rapidly fatal)  MOST bone tumors are benign lesions  Most benign lesions are seen <30 years of age  A new bone tumor in the elderly is more likely to be malignant  No bone is safe (though most primaries are in long bones)  Locale in the bone gives important Dx info  More common benign lesions typically present as incidental findings (non-painful, stable size)  Be cautious with painful lesions and those that grow relatively fast (over weeks or months)  Pathological fracture can be the first sign of tumor
  • 3.  Bone neoplasms are very difficult to diagnose specifically on radiologic testing alone  So why is radiology important?  Exact location of lesion  Extent of growth/metastasis  Aggressiveness  Best test for Dx= X-ray  Best test for staging= CT or MRI  Quick shout out to the pathologists– histologic grade is the most important prognostic feature of bone sarcomas and essential for staging most of the bone tumor types.
  • 6. Case I  16 yr old white male with pain in his left upper arm.  Mild swelling and tenderness  Pain progressively getting worse for ~ 3 months  Recent onset of mild fever
  • 10. Biopsy material showed a highly cellular, infiltrative neoplasm consisting of sheets of tightly packed, round cells with very scant cytoplasm ("round blue cell tumor"). Occasional Homer-Wright rosettes were identified. Other fields showed extensive necrosis.
  • 14. Dx: Ewing’s Sarcoma (or PNET)  #2 primary bone malignancy in kids (5-15 is most common age group  Much more common in Caucasians  Typically in the diaphysis of long tubular bones or in large flat bone  Lytic tumor w/ permeative margins extending into the soft tissue  Periostial rxn creates sheets of reactive bone in an onion-skin fashion
  • 15. Another most excellent example of “onion- skinning”
  • 16. Case II  33 yr old black female with sudden severe hand pain after very minor trauma.  Completely healthy otherwise.  All labs normal
  • 19. Dx: Enchondroma  Benign cartilagenous tumors but hard to distinguish from a low grade chondrosarcoma  Acral bones-- the most common primary hand tumor  Usually solitary, usually incidental finding (non- painful unless associated with fracture)  Get hand films and look for dec. lucency but not so much as a cyst (more ground-glass) w/ or w/o areas of stippled calcifications or rings
  • 20. For boards and wards:  Multiple enchondromas = ____________  Multiple enchondromas + hemanigiomas of soft tissue = _____________
  • 21. For boards and wards:  Multiple enchondromas = Ollier’s Dz  Multiple enchondromas + hemangiomas of soft tissue = Maffucci syndrome
  • 22. Case III  50 yr old white male with back pain  Mainly lower spine/sacral pain, progressive ~ 8 months  New onset rectal pain and constipation
  • 25. CT guided FNA confirmed…
  • 26. Dx: Chordoma  Arises from notochord remnants. Thus is typically midline along the spine and usually at the ends (Sacrococc or occ/cervical jxn)  Males>Females, middle age  + staining w/ S-100 and epithelial markers  Locally invasive until very late in disease where mets can go to the lungs, LN, skin.
  • 27. Case IV  21 yr old male with new onset chest pain today, worse on inhalation.  ROS significant for an ongoing aching leg pain for the past 6 months which he has put off seeing a doctor for.
  • 32. Dx: The dreaded Osteosarcoma  #1 primary bone malignancy  Associated with RB1 and p53 gene mutations  1000x greater risk w/ Hx of hereditary retinoblastoma  Member of the Li-Fraumeni Syndrome family  Bimodal age spike: young and elderly  75% <age 20  Osteosarcoma in elderly usually from predisposing mechanism (secondary)  Paget Dz, bone infarcts, history of radiation, etc Most patients die from pulmonary complications after metastatic seeding of the lungs (ex: pneumothorax)
  • 33.  Metaphysial tumor  60% at the knee (distal femur or prox tibia)  Radiographic terms to know:  Codman’s Triangle:  “Sunburst” periostial formation:  AKA “Hair on end”
  • 34. For the future Surgeons:  Rotationplasty is a new solution to disfiguring surgical resections of lower limb sarcomas:
  • 36. Incidental finding on knee xray Fabella = posterior sesmoids or little confused knee caps
  • 37. 13 yr old boy with superior tibial pain, r/o neoplasm w/ xray shows: Osgood Schlatter
  • 38. Metastatic Disease  Most common malignant lesion of bone  Bone is # 3 on the list of favorite places for mobile cancers to go  Malignant lesions are more likely to be in axial bones  Typically multifocal BUT renal and thyroid carcinomas are notorious for producing only a solitary lesion  Can be lytic, blastic, or both:  Lung is Lytic, Prostate Produces, Breast does Both
  • 39. Mets (cont)  Adults  Lung  Prostate  Breast  Kidney  Kids  NB  Wilm’s  OS  Ewing’s  Rhabdomyosarcoma