Oral manifestations of systemic diseases Flashcards
What is wegners granulomatosis
autoimmune disorder of unknown etiology resulting in systemic vasculitis and necrotizinf granulomatous lesions of the respiratory tract
What is the most characteristic oral manifestation of wegeners granulomatosis
Strawberry gingivitis florid granular hyperplasia (bumpy hemorrhagic and friable) reported boine destruction and tooth mobility
What are you looking for in indirect immunoflourescence for Wegener
c-ANCA clasic anti neutrophil cytoplastic antibodies diffuse cytoplasmic staining pattern
IN Wegner what are you looking for with ELISA (Enzyme linked immunosorbent assay
ID antibodies against proteinase 3 confirms positive indirect immunoflourescence
What are the halmarks of hyperparathyroidism
Stones bones groans moans brown tumor
In hyperparathyroidism what does Stones mean
Kidney stones metastatic calcification within other soft tissue: blood vessel walls sclera, dura, subcutaneous
In hyperparathyroidism what does bones mean
subperiosteal resorption of phalanges loss of lamina dura around tooth roos alterations of bony trabecular pattern (ground glass)
What is a brown tumor
Name derived from gross apearance due to hemorrhage and hemosiderin well delineated, uni or multilocular radiolucencies mandible clavicles pelvis ribs histology is identical to central giant cell lesion
What is osteitis fibrosa cystica
central fibrosis/degredation of brown tumors
What is renal osteodystrophy
end stage renal disease with striking jaw enlargement ground glass appearance can cause secondary hyperparathyroidism
Whats the def of amyloidosis
a heterogenous group of conditions characterized by the deposition of an extracellular proteinaceous substance (amyloid)
How is amyloidosis classified
organ limited systemic
what is an amyloid nodule
solitary asymptomatic submucosal deposit composed of aggregates of immunoglobulin light chains focal collections of monoclonal plasma cells may be responsible not associated with systemic alteration this type is RARE in oral soft tissues
amyloidosis and multiple myeloma
shared in 15-20% of cases
Symptoms of systemic amyloidosis
inisital non specific skin lesions then smooth surfaced firm waxy papules/plaques on eyelid retroauricular region, neck, lips Macroglossia difuse or nodular enlargement of tongue (may be ulcerated) Xerostomia and xerophtalmia if amyloid deposits in the lacrimal and salivary glands