6-Osteodystrophy unknown causes Flashcards
What is Paget’s disease?
accelerated resorption and deposition of bone, osteoblasts win and bones become sclerotic, larger and brittle; white male, polyostotic
How does Paget’s disease appear radiographically?
cotton wool-like radiopacity, generalized hypercementosis
Complications of Paget’s disease?
fracture, malignant transformation, 1% develop osteogenic carcinoma
What is Fibrous Dysplasia?
Starts a large cascade and eventually cAMP, affects differentiation of proteoblasts, prolonged activation stimulates endocrine receptors, bones become replaced with fibrous tissue and immature bone
Fibrious dysplasia monostotic or polyostotic?
Monostotic
What is Jaffe-Lichtenstein Syndrome?
Fibrous dysplasia polyostotic with cafe au lait spots
What is McCune-Albright Syndrome?
Fibrous dysplasia polyostotic with cafe au lait AND endocrinopathy
Clinical features of Fibrous dysplasia?
Young - 1-2 decades Long bone pain/fracture Craniofacial expansion/disfigurement CFFD = Compress vital structures Like optic nerve - blindness
Clinical features of McCune-Albright Syndrome?
Hyperendocrine function such as gonads
Radiographic appearance of Fibrous dysplasia?
early lesions lucent->mixed->ground glass opacity
Fibrous dysplasia treatment?
FD stabilizes so bad ones recontour
General characteristics of Central Giant Cell Granuloma?
Females Before age 30 - young Md 70% Anterior jaws classically crossed midline
Describe nonaggressive Central Giant Cell Granuloma?
asymptomatic, slow growth, nor cortical perforation or root resorption
Describe aggressive Central Giant Cell Granuloma?
Pain, rapid growth, cortical perforation and root resorption
Radiographic appearance of Central Giant Cell Granuloma?
unilocular/multilocular
noncorticated margins
cortical perforation or expansion
root resorption