Pathology of Bone and Joints

  1. Pannus are found in which type of arthritis?
    RA
  2. Eroding cartilage occurs in which type of arthritis?
    RA
  3. Fibrous ankylosis are found in which type of arthritis?
    RA
  4. Bony ankylosis are found in which type of arthritis?
    RA
  5. Bony spurs are found in which type of arthritis?
    Osteoarthritis
  6. Subchondral cysts are found in which type of arthritis?
    Osteoarthritis
  7. Subchondral sclerosis are found in which type of arthritis?
    Osteoarthritis
  8. Osteophytes are found in which type of arthritis?
    Osteoarthritis
  9. Thinned fibrillated cartilages are found in which type of arthritis?
    Osteoarthritis
  10. What is found underneath pannus in RA joint?
    Immune cells
  11. What is the crystal composition found in gout?
    Uric acid
  12. What is the crystal composition found in pseudogout?
    Calcium pyrophosphate
  13. What is the shape of the crystal in gout?
    Needle-like
  14. What is the shape of the crystal in pseudogout?
    Rhomboid
  15. What is the most commonly affected joint in gout?
    First MTP
  16. What is the most commonly affected joint in pseudogout?
    Knee
  17. What is the first line of treatment for gout?
    NSAID
  18. What is the first line of treatment for pseudogout?
    NSAID
  19. What is the radiographic appearance of gout?
    Rat-bite erosions
  20. What is the radiographic appearance of pseudogout?
    White lines of chondrocalcinosis
  21. Is gout birefringent negative or positive?
    Negative
  22. Is pseudogout birefringent negative or positive?
    Weakly positive
  23. What is primary hyperparathyroidism?
    autonomous hyperplasia or tumor of parathyroid gland
  24. What is secondary hyperparathyroidism?
    Prolonged states of hypocalcemia resulting in compensatory hypersecretion of PTH
  25. What cells sense parathyroid hormone levels?
    Osteoblasts
  26. What are the symptoms of hyperparathyroidism?
    Osteoporosis, brown tumors, osteitis fibrosa cystica
  27. Is hyperparathyroidism reversible?
    Yes, reduction in PTH levels to normal can reverse bone changes
  28. What is the characteristic of brown tumor?
    • Microfracture with secondary hemoorhage
    • Influx of macrophages
    • Ingrowth of reactive fibrous tissue
    • Brown is vascularity, hemorrhage, hemosidering
  29. What is another name of osteonecrosis?
    Avascular necrosis
  30. What is osteonecrosis?
    Infraction of bone and marrow due to ischemia
  31. What causes ischemia that leads to osteonecrosis?
    Fractures, steroids, thrombosis, vessel injury, increased intraosseus pressure, venous hypertension
  32. What are some conditions associated with osteonecrosis?
    • Alcohol abuse
    • CT disorders
    • Corticosteroid administration
    • Chronic pancreatitis
    • Bends
    • Infection
    • Pregnancy
    • Sickle cell crisis
    • Trauma
    • Tumors
  33. What is the morphology of avascular necrosis (osteonecrosis)
    • Subchondral infarcts
    • Recognize pictures of a line underneath the articular cartilage
  34. What is achondroplasia?
    Most common Disease of growth plate and major cause of dwarfism
  35. What causes achondroplasia?
    • Defect in cell signaling leading to reduction in chondrocyte proliferation
    • Point mutation in gene FGF receptor 3 gain-of-function mutation (related to increased paternal age)
  36. What happens when there is an over expression in FGFR3 (autosomal dominant mutation)?
    Inhibits growth—cause of achondroplasia
  37. What are symptoms of achondroplasia?
    • Infants with shortened proximal extremities
    • Trunk of relative normal length
    • Enlarged head with bulging forehead
    • Not associated with longevity, intelligence or reproductive status
  38. What is another name for osteopetrosis?
    • Marble bone disease
    • Albers-schonberg disease
  39. What is osteopetrosis?
    Rare hereditary group of disorders with reduced osteoclastic bone resorption resulting in diffuse symmetrical skeletal sclerosis
  40. What are the characteristics of osteopetrosis?
    Bones are stonelike but very brittle (dissolvable), break like chalk
  41. What is the cause of osteoclast dysfunction in osteopetrosis?
    Carbonic anhydrase deficiency
  42. What is the morphology of osteopetrosis?
    • bones lack medullary canal, erlenmyfer flask deformity
    • no room for hematopoietic marrow
  43. What are physiological results of osteopetrosis?
    • Pancytopenia
    • Extramedullary hematopoiesis
    • Renal tubular acidosis with carbonic anhydrase (decreased tubular resorption- metabolic acidosis)
  44. True/false: osteopetrosis can be either autosomal recessive or autosomal dominant
    True
  45. When does autosomal recessive osteopetrosis typically diagnosed?
    • In utero/ soon after birth
    • Pt survive to infancy but with cranial nerve problems
  46. What does autosomal dominant osteopetrosis typically diagnosed?
    Adolescence to early adulthood
  47. What is a treatment for osteopetrosis?
    Bone marrow transplant to provide progenitor cells
  48. Is osteogenesis imperfecta a Type 1 collagen disease?
    Yes
  49. What is type 1 collagen disease?
    Caused by deficiency in synthesis of type 1 collagen
  50. What is an example of type 1 collagen disease
    Osteogenesis imperfecta (brittle bone disease)
  51. What is osteogenesis imperfecta?
    Mutated genes coding for a1 and a2 chains of collagen
  52. What are the symptoms of osteogenesis imperfecta?
    Prominent skeletal manifestations with joints, eyes, ears, skin and teeth affected as well
  53. Which subtype of osteogenesis imperfecta is lethal?
    Type 2
  54. How is paget diagnosed from lab tests?
    • Elevated serum alkaline phosphatase
    • Increased urinary excretion of hydroxyproline
  55. What can be seen on a bone scan in osteogenesis paget?
    Anterior bowing of femora and tibia
  56. What is characteristic of Paget?
    • Chalkstick-like fractures in long bones of lower extremities
    • Recognize the jigsaw puzzle histology picture
  57. What is primary gout?
    Hyperproduction of uric acid or underexcretion of uric acid
  58. True/false: not all persons who have hyperuricemia have gout?
    True
  59. What is a distinguishing clinical feature of gout?
    Tophi
  60. What is another name for osteoarthritis?
    Degenerative joint disease
  61. What are pathologic features of osteoarthritis?
    • Often affects cervical or lumbar area
    • Hand involvement
    • Feet involvement
  62. What is the name for when osteophyte or bone spurs form in osteoarthritis that causes stiffness of vertebral column?
    Lipping
  63. Heberden’s nodules in osteoarthritis involves which joint?
    DIP joints
  64. Bouchard’s nodules involves which joint?
    PIP joints
  65. What is osteoarthritis of the foot?
    Bunions
  66. What type of joint is involved in RA?
    Synovial joints
  67. Is RA symmetrical or asymmetrical involvement of joints?
    Symmetrical
  68. What are rheumatoid nodules?
    Subcutaneous nodules composed of central fibrinoid necrosis surrounded by macrophages and lymphocytes
  69. What is Reiter Syndrome?
    Also known as reactive arthritis
  70. What are the symptoms of reactive arthritis?
    • Seronegative polyarthritis
    • Conjunctivitis/ uveitis
    • Nonspecific urethritis
  71. What is osteosarcoma?
    • Malignant bone tumor
    • Common in boys 10-20 years
  72. Common locations for osteosarcoma?
    • Knee
    • Metaphysis of long bone
    • Proximal humerus
  73. What are some x-ray findings of osteosarcoma?
    • Bone destruction and neoplastic bone formation
    • Periosteum produces a incomplete rim of reactive bone
  74. What is Ewing Sarcoma?
    Uncommon malignant bone tumor
  75. What type of cells composes ewing sarcoma?
    Small, round blue cells
  76. Where does ewing sarcom arise from?
    • Primitive marrow elements
    • Immature mesenchymal cells
    • Tumor of long bones, mid-shaf or metaphyseal tumor
  77. What gene is involved in ewing sarcoma?
    • Reciprocal translocation between chromosome 11 and 22
    • Fusion protein EQS/FLI-1
  78. What is the genetic involvement in chondrosarcomas
    Trisomy 7
  79. What is multiple myeloma?
    • Malignant tumor of plasma cells
    • Recruit osteoclasts that causes lytic bone lesions
  80. Which bones are commonly involved in multiple myeloma?
    • Skull (punched out lesions)
    • Spine
    • Ribs
    • Pelvis
    • Femur
  81. What is characteristic of pathology finding in multiple myeloma?
    • Amyloid deposits
    • Sheets of plasma cells
Author
lykthrnn
ID
343218
Card Set
Pathology of Bone and Joints
Description
NMSK Exam 2 Pathology
Updated