Your SlideShare is downloading. ×
0
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Paget disease
Upcoming SlideShare
Loading in...5
×

Thanks for flagging this SlideShare!

Oops! An error has occurred.

×
Saving this for later? Get the SlideShare app to save on your phone or tablet. Read anywhere, anytime – even offline.
Text the download link to your phone
Standard text messaging rates apply

Paget disease

1,234

Published on

Published in: Health & Medicine, Technology
1 Comment
6 Likes
Statistics
Notes
No Downloads
Views
Total Views
1,234
On Slideshare
0
From Embeds
0
Number of Embeds
0
Actions
Shares
0
Downloads
97
Comments
1
Likes
6
Embeds 0
No embeds

Report content
Flagged as inappropriate Flag as inappropriate
Flag as inappropriate

Select your reason for flagging this presentation as inappropriate.

Cancel
No notes for slide

Transcript

  • 1. Definition • Paget disease is a chronic metabolic bone disorder characterized by imbalance between bone resorption & new bone formation. • It is chronic metabolic bone disorder characterized by abnormal osseous remodelling.
  • 2. Incidence • • • • It is common in England. It is uncommon in Egypt and Middle East. Age: it affects older persons. Sex: more common in males.
  • 3. Etiology • Unknown. • but recent hypothesis claims that it is due to slow virus infection (due to the presence of intranuclear inclusion bodies in the osteoclasts).
  • 4. Pathology Paget disease is divided into 3 phases: 1. Hot phase. 2. Intermediate phase. 3. Cool phase. These 3 phases represent a continuum not separate phases.
  • 5. Hot phase Osteolytic phase Incipien Osteoclas & cause bone t phase ts resorption. predomina te Intermediate phase Mixed phase Active phase Osteoblas cause bone ts repair superimpose d on bone resorption. Cool phase Blastic phase Non active phase Osteoblas & cause new ts bone predomina formation. te
  • 6. C.P
  • 7. Location • Monostotic or polystotic (more common) forms. It is more common in the axial skeleton • with the most common sites being • pelvis, skull & spine. Proximal long bones are also frequently affected • with the most common among them proximal femur. Paget disease of long bones begins in the subchondral region of end & advances to the other end.
  • 8. Hot phase • Initial phase of increased osteoclastic activity that affects both the cortex and cancellous bone.
  • 9. Radiological manifestations • Flat bones: osteoporosis circumscripta. • There is no surrounding sclerosis (as there is no osteoblastic activity in this phase)
  • 10. • Long bone: • candle flame or blade of grass appearance. Advancing wedge
  • 11. Intermediate phase (mixed phase) • Bone destruction accompanied by new bone formation.
  • 12. Radiological manifestations • Pelvis: Cortical thickening and sclerosis of the iliopectineal and ischio-pubic lines, resulting in obliteration of the tear drop.
  • 13. • Vertebrae: Picture frame appearance Cystic spongiosa Cortical thickening. Coarse trabecular pattern.
  • 14. • Long bones: • Cortical thickening. • Coarse trabecular pattern.
  • 15. Cold phase • Disorganized new bone formation
  • 16. • Skull: • Cotton wool appearance
  • 17. • Pelvis:
  • 18. • Spine: • Ivory vertebra
  • 19. • Long bones:
  • 20. Bone scan • Typically demonstrates marked increased uptake of radiotracer in all phases
  • 21. Active phase Mixed phase Inactive phase The fatty bone marrow is replaced by fibrovascular granulation tissue giving speckled appearance. Yellow marrow fat signal intensity is maintained or even more bright as the marrow space of pagetic bone actually has more fat than found in the uninvolved bone, The fatty bone marrow is replaced by increased medullary bone formation T1 Low signal Bright signal Low signal. T2 Bright signal. (more obvious on STIR) Bright signal Low signal
  • 22. Contrast enhanced MRI • Intracortical and speckled intramedullary enhancement due to increased blood flow. +C

×