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Flashcards

Path bone pathology (2)

Katie Hayes SP D2 Inglês 34 flashcards

Flashcards do conjunto (34)

  1. 1focal osteoporotic bone marrow defect hematopoeitic bone marrow defectasymptomatic UL RL with trabeculations visible running thru
    post mandible
    no expansion
    adult females
    hist: hematopoietic or fatty bone marrow
  2. 2idiopathic osteosclerosisfocal area of incr radiodensity
    sharply demarcated with no RL rim
    unknown cause (no pathosis)
    asymptomatic, non-expansile
    VITAL mand M and PM area (not restricted to jaws)
    young people
    histo: sclerotic vital bone (biopsy not indicated tho)
  3. 3condensing osteitis chronic focal sclerosing osteomyelitisfocal opacity assoc with pathosis
    well-defined, no RL border
    NON VITAL mand M and PM
    not separated from apex of tooth
    young adults
  4. 4retained root tipwell demarcated RO
  5. 5socket sclerosisdense bone formed in area of extraction
    form of osteosclerosis
  6. 6sub-pontic osseous hyperplasiareactive condition which causes hyperplastic production of bone beneath pontic
    tx: sg
  7. 7gardner syndromeAD
    presents with osteomas and jaw densities, supernumerary teeth, intestinal polyps with malig transformation (adenocarcinoma)
  8. 8pseudocyst of maxillary sinus antral pseudocystRO dome shaped lesion in maxillary sinus
    NO BIOPSY
  9. 9submandibular salivary gland cyst stafne cyst static bone cavity latent bone cystnot a true cyst (no epi lining)
    lingual development defect--lobe of SM gland fills
    well-defined RL between mand canal and inf border
    no tx
  10. 10traumatic bone cyst idiopathic bone cavity hemmorhagic bone cyst simple bone cystNOT A TRUE CYST (no epi lining)
    due to trauma/hemorrhage
    mostly male teens/yg adults
    mandible
    asymptomatic RL with scalloped border
    rare expansion
    surround vital teeth (no root resorb)
    biopsy initiates healing
  11. 11aneurysmal bone cystNOT A TRUE CYST
    RL, often ML
    rapidly growing, may blow out cortex
    painful
    mandible (or any bone)
    young individuals <20 yrs
    ballooning dilation of bone, "blood soaked sponge" appearance
    hemosiderin staining
    histo: cyst like cavity filled with blood and multinucleated giant cells
  12. 12osteogenesis imperfecta brittle bone ds lobstein dsAD or AR defective synthesis of type 1 collagen
    extreme bone fragility, deformity, short, joint laxity
    skull: too little bone, cortical thinning, attenuate trabeculae
    blue sclera
    dentigerous imperfecta: bluish discoloration, obliteration of pulp
    may be misdx as child abuse
    tx: bisphosphonates (risk of MRONJ)
  13. 13osteopetrosis marble bone disease albers schoneberg dsrare genetic ds in which bone density is incr
    AR infantile is most severe, AD adult is least severe
    reduced osteoclast bone resorption (reduced acid profuction) resulting in diffuse, symmetric sclerosis
    progressive obliteration of bone marrow-->neutropenia, anemia, extramed hematopoeisis
    easy fracture
    narrowing of skull foramina-->blind, deaf, paralysis, venous drain
    delayed tooth eruption
    osteomyelitis
    tx: hematopoetic cell transplant
  14. 14osteomyelitis vs osteonecrosisosteomyelitis: vital bone with inflammatory cells in marrow spaces
    osteonecrosis: nonvital bone with bact debris in marrow spaces
  15. 15Paget's ds of bone osteitis deformansexcessive remodeling of bone caused by osteoclast dysfunction (NF-kb mutation)
    possible paramyxovirus origin
    progression from initial lytic stage (RL)-->mixed lytic-sclerotic --> late sclerotic (RO)
    older individuals
    monostotic or polyostotic
    impinges on foramina-->pain, headache, visual dist
    change in hat size, denture fit
    enlarge skull, maxilla enlargement (lion's face)
    "cotton wool" bone and hypercementosis
    complications: osteomyelitis, osteosarcoma, bowing of legs, path fracture, CF
    tx: bisphospohonates (MRONJ), calcitonin
    hist: reversal lines, mosaic jigsaw pattern
  16. 16benign fibro-osseous lesions fibrous dysplasia osseous dysplasia ossifying fibromanormal bone replaced with mineralized fibrous CT
    origins: devl, reactive, neoplasms
    RL or RO unilateral enlargement
    ground glass appearance
    monostotic (Craniofacial) > polyostotic (mcune albright, jaffe lichenstein)
    histo: chinese characters
  17. 17McCune Albright syndromesevere form of fibrous dysplasia
    Bone lesions: bowing legs, shepards hook, ground glass with expansion
    skin: cafe au lait
    endocrinopathy
  18. 18Jaffe-Lichenstein Syndromemild form of fibrous dysplasia
    Bone lesions: bowing legs, shepards hook, ground glass with expansion
    skin: cafe au lait
  19. 19cemento osseous dysplasiareactive benign fibro-osseous lesion (most common)
    arises from PDL elements
    spectrum of ds from localized to generalized
    cementum and bone depositions
  20. 20PA Cemento-osseous dysplasiabenign fibrosseous lesion in PA of ant mandible
    black females 30-50 yo
    aymptomatic, assoc with vital teeth
    RL --> mixed --> RO
    multiple >> solitary lesions
  21. 21florid cemento-osseous dysplasiabenign fibrosseous lesion with multifocal involvement, often bilateral and symm
    black females 30-50 yo
    aymptomatic, assoc with vital teeth
    RL --> mixed --> RO with thin RL outline
  22. 22focal cemento-osseous dysplasiabenign fibrosseous lesion in post mandible and extraction sites
    middle aged adults
    aymptomatic, assoc with vital teeth
    thin peripheral RL rim "bullseye"
  23. 23cemento-ossifying fibromabenign neoplasm, fibro-osseous lesion
    middle aged females
    M and PM of mandible
    RL and mixed
    expansion may displace teeth
    biopsy comes out in one complete piece
  24. 24cherubismAD condition in kids
    bilateral jaw RL with giant cell histo
    over time lesions may resolve
    histo: multinucleated giant cells
  25. 25central giant cell granulomaUL or ML solitary RL in anterior jaw, crossing midline
    10-30 yo females
    cortical expansion with perf uncommon, resorption of tooth roots
    tx: curretage + corticosteroids/calcitonin/IF A2
    histo: multinucleated giant cells
  26. 26browns tumor of hyperparathyroidismsame radio and histo as CGCG
    blood levels indicate hyper parathyroidism: incr serum ca, decr serum phos, incr PTH
  27. 27giant cell tumor of long bonetrue neoplasm, ML RL
    found in epiphyseas of long bones of adults
    metastasis to lung
  28. 28langerhans cell histiocytosisneoplastic prolif of histiocytes
    "floating teeth" and punched out RL
    chronic focal: solitary lesion in bone
    chronic disseminated (hands schuller christian): multiple bones, organs, lymph nodes, skin
    acute disseminated: affects kids, organs, bone marrow, skin
    histo: histocytes with birbeck granulaes
  29. 29metaplastic carcinomamost common malig neoplasm in bone
  30. 30osteosarcomamost common malig neoplasm arising FROM bone
    bone/osteoid, chrondroid, and collagen
    most common in long bones around knees
    pain, swelling
    hx of extraction
    lytic or sclerotic; sunburst appearance, ill-defined margins, widened PDL
    tx: sg and chemo
    complicates pagets
  31. 31post irridation bone sarcomarelated to radiation dose
    causes osteosarcoma, fibrosarcoma, chrondosarcoma
    hist and prog identical to de novo tumors
  32. 32chrondosarcomamalig neoplasm in which cartilage is formed by malig stroma
    maxilla
    widened PDL with opaque bone appearance; sunburst
  33. 33ewing sarcomamalignancy of young people
    pain, swelling
    mimics infec with fever, leukocytes, elev ESR
    pelvis and lower extremeties most common
    onion skin periosteal rxn
    translocation T(11:22)
    chemo + sg/radio
  34. 34multiple myelomamost common neoplasm arising WITHIN bone
    disseminated neoplasm of terminally differentiated B-cells
    multiple lytic lesion, hypercalcemia, bone pain
    punched out RL, lose teeth, pain, amyloidosis, path frac
    lab: elev serum ca, prot, Ig; elev ESR, rouleaux, M spike
    may lead to renal failure, infec, anemia

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SP D2 FlashCards sobre Path bone pathology (2), criado por Katie Hayes em 03-04-2020.
Criado por
Katie Hayes
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