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PATHOLOGY..

 Paget’s Disease
INTRODUCTION
Paget’s disease is a chronic condition of bone
characterized by disorder of the normal bone
remodeling process.
Characterized by excessive breakdown of bone
tissue followed by abnormal bone formation.
Also known as Osteitis Deformans is a bone
disease unknown cause.
Affecting men twice as freaquently as women.
Named after the England Surgeons Sir James
Paget.
DISEASE CLASSIFICATION

 INFLAMMATORY
                                  CONGENTIAL
     DISEASE




•Multifocal chronic
                              •Certain of genes may
skeletal disease due to
                              Been associated with
Chronic paramyxoviral
                              Paget’s disease, including
Virus infection.
                              The Sequestrosome 1
•As a result, the bone that
                              Gene On Chromosome 5.
is formed is abnormal.
ETIOLOGY
The cause of Paget’s disease is unknown.
Disease may be caused by a virus.
Paramyxovirus infection of osteoblasts may
activate of the c-fos proto-oncogene,
resulting in localized abnormal osteoclastic
activity typical of paget’s disease.
Also, a person’s genes may predispose them
to developing paget’s disease.
 Paget’s disease affects older skeletal bone
  of adults.
 There is also an extremely rare form of
  paget’s disease in children, referred to as
  Juvenile Paget’s disease.
Pathogenesis
   Hyper vascular/                 Initial phase of
   Osteolytic phase               Disorder involves
                                  Bone resorption by
 Abnormal matrix                     osteoclasts
Persists but cellular
 Activity is nearly
      Absent.                                           Intermediate
                           Paget’s disease
                                                            phase


            Exhaustive               Osteoclytic activity
             (burn out)                       +
               stage                 Osteoblastic activity
MANIFESTATIONS - SYMPTOMS
Paget’s disease is more commonly asymptomatic,
but may exhibit a variety of non-specific
symptoms due to increased bone turnover.
The bones that are move commonly affected
include the pelvis, spine, skull, and the long bone.
Individuals may experience any or a combination
of the following symptoms;
  Bone pain
  fractures
Skeletal Deformities – bowed legs, Fronto-
occipital skull enlargement.
Warm sensation – due to increased blood
supply to abnormal bones.
Nerve damage – hearing loss, visual
abnormalities.
Cardiac abnormalities – shortness of breath.
MANIFESTATIONS - SIGN
Signs may be bitemporal skull
enlargement with frontal “bossing”,
diluted scalp veins, nerve deafness in one
or both ears.
Also angioid streaks in the fundus of the
eyes and a short kyphotic trunk.
SIGNIFICANT LAB TESTS
Blood chemistry (blood patient who have
paget’s disease) results indicate very high
alkaline phosphates levels with normal
serum calcium and phosphorus.
There is no known cure for this disease.
Most cases are mild and asymptomatic no
treatment is necessary in symptomatic
cases medications.
IMAGING CONSIDERATION

 X-ray of the skull, spine, pelvis and long
  bone.
 CT scan
 MRI (Magnetic Resonance Imaging)
 Radionuclide bone scan or RNI
  (Radionuclide Imaging).
RADIOLOGICAL APPEARANCE
Radionuclide bone scans readily detect
Paget’s disease even in its very early stage.
Radiographically the affected bone
typically demonstrate cortical thickening,
with a coarse, thickened trabecular pattern.
Mixed areas of radiolucent Osteolysis and
radiopaque Osteosclerosis may be seen.
   Radiograph of the
    fibula and tibia of the
    patient in figure
    demonstrating       the
    effect of advanced
    proliferative Paget’s
    disease on the fibula
    and tibia.
Paget’s disease on pelvis…

                  Paget’s        disease
                   involving the left
                   hemi pelvis and right,
                   there      is   severe
                   osteoarthritis of the
                   left hip but a
                   relatively     normal
                   joint space in the
                   right hip.
Paget’s disease….
References…
 http://www.nlm.nih.gov
 http://www.medicinet.com
 http://www.uncomparehealthcare.com
 http://www.wheelessonline.com
 http://www.e-radiography.net
 http://www.radiographics.highwive.org
paget's disease

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paget's disease

  • 2. INTRODUCTION Paget’s disease is a chronic condition of bone characterized by disorder of the normal bone remodeling process. Characterized by excessive breakdown of bone tissue followed by abnormal bone formation. Also known as Osteitis Deformans is a bone disease unknown cause. Affecting men twice as freaquently as women. Named after the England Surgeons Sir James Paget.
  • 3. DISEASE CLASSIFICATION INFLAMMATORY CONGENTIAL DISEASE •Multifocal chronic •Certain of genes may skeletal disease due to Been associated with Chronic paramyxoviral Paget’s disease, including Virus infection. The Sequestrosome 1 •As a result, the bone that Gene On Chromosome 5. is formed is abnormal.
  • 4. ETIOLOGY The cause of Paget’s disease is unknown. Disease may be caused by a virus. Paramyxovirus infection of osteoblasts may activate of the c-fos proto-oncogene, resulting in localized abnormal osteoclastic activity typical of paget’s disease. Also, a person’s genes may predispose them to developing paget’s disease.
  • 5.  Paget’s disease affects older skeletal bone of adults.  There is also an extremely rare form of paget’s disease in children, referred to as Juvenile Paget’s disease.
  • 6. Pathogenesis Hyper vascular/ Initial phase of Osteolytic phase Disorder involves Bone resorption by Abnormal matrix osteoclasts Persists but cellular Activity is nearly Absent. Intermediate Paget’s disease phase Exhaustive Osteoclytic activity (burn out) + stage Osteoblastic activity
  • 7. MANIFESTATIONS - SYMPTOMS Paget’s disease is more commonly asymptomatic, but may exhibit a variety of non-specific symptoms due to increased bone turnover. The bones that are move commonly affected include the pelvis, spine, skull, and the long bone. Individuals may experience any or a combination of the following symptoms; Bone pain fractures
  • 8. Skeletal Deformities – bowed legs, Fronto- occipital skull enlargement. Warm sensation – due to increased blood supply to abnormal bones. Nerve damage – hearing loss, visual abnormalities. Cardiac abnormalities – shortness of breath.
  • 9. MANIFESTATIONS - SIGN Signs may be bitemporal skull enlargement with frontal “bossing”, diluted scalp veins, nerve deafness in one or both ears. Also angioid streaks in the fundus of the eyes and a short kyphotic trunk.
  • 10. SIGNIFICANT LAB TESTS Blood chemistry (blood patient who have paget’s disease) results indicate very high alkaline phosphates levels with normal serum calcium and phosphorus. There is no known cure for this disease. Most cases are mild and asymptomatic no treatment is necessary in symptomatic cases medications.
  • 11. IMAGING CONSIDERATION  X-ray of the skull, spine, pelvis and long bone.  CT scan  MRI (Magnetic Resonance Imaging)  Radionuclide bone scan or RNI (Radionuclide Imaging).
  • 12. RADIOLOGICAL APPEARANCE Radionuclide bone scans readily detect Paget’s disease even in its very early stage. Radiographically the affected bone typically demonstrate cortical thickening, with a coarse, thickened trabecular pattern. Mixed areas of radiolucent Osteolysis and radiopaque Osteosclerosis may be seen.
  • 13. Radiograph of the fibula and tibia of the patient in figure demonstrating the effect of advanced proliferative Paget’s disease on the fibula and tibia.
  • 14. Paget’s disease on pelvis…  Paget’s disease involving the left hemi pelvis and right, there is severe osteoarthritis of the left hip but a relatively normal joint space in the right hip.
  • 16. References… http://www.nlm.nih.gov http://www.medicinet.com http://www.uncomparehealthcare.com http://www.wheelessonline.com http://www.e-radiography.net http://www.radiographics.highwive.org