Bone Pathology Flashcards

1
Q

What is Osteoporosis

A

Osteoporosis is a health condition that weakens bones, making them fragile and more likely to break. It develops slowly over several years and is often only diagnosed when a fall or sudden impact causes a bone to break (fracture).

  • DIminisehd bone mass
  • Disruption of microarchitecture
  • Loss of trabeculae
  • diminished bone strength
  • Increased suscpetibility to insufficiency fractures
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2
Q

Embryonology of the parts of the bones

A
  • Bone -develops from mesoderm (mesenchyme)
  • Axial skeleton - from somites
  • Appendicular skeleton from lateral mesoderm
  • Cranial skeleton - directly from
  • Mesenchyma - membranous bones
  • Rest - throigj intermediate hyalien cartilage
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3
Q

What is osteogenesis and ossification

A
  • Osteogenesis = whole process of development of an bone from mesenchyme
  • Ossification = selective process of hardenign or radiological/histiological evidence of bone formation from membrane or crtilage
  • Membranous ossification, Endochondral ossification, Osteogensis imperfecta.
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4
Q

What are the Classifications of bones:

A
  • Anatomical - long, flat
  • Structural:
    • Macroscopic - cortical/comapct and cancellous/spongy
    • Hisitiological - lamellar and woven
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5
Q

Bone histology:

A
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6
Q
A
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7
Q

Decsribe Woven Bone

A
  • Not an orderly paralll array
  • Intersecting, crisscross and woven arrangement
  • Iregular thick and thin bundles
  • Seen in foetus
  • Recapitulated in fracture healing
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8
Q

Describe the Parts of a long bone

A
  • Diaphysis - shaft (primary centre of ossification)
  • Metaphysis - below the growht plate
  • Epiphysis - upon/above the growht plate (secondary centre of ossification)
  • Physis - growth (plate)
  • Nutrient artery = through nutrient foramen - directed away from growing end- ‘to elbow i go, from the knee i flee- Milekrs position)
    *
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9
Q

Where does provisional calcification start in the growth plate?

A
  • Upper and lower hypertrophic zone
  • Provisional calcification starts in latter which is storngest layer of growth plate compared to upper hyp zone which is the weakest and usually involved in growth plate injuries
  • Zone of endochondral ossification - intense calcification and in continuity with metaphysis 4
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10
Q

What are the ones labelled G,H,O,R

A

G = Growth zone

H= hypertorphic zone

0 = ossification zone

R= Remodelling zone

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11
Q

What are labelled

A

Osteoid and osteoclasts

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12
Q

What is the sequence of longitudinal growth in long bone

A
  1. By provisional calcification of cartilage - endochondral ossification:
  2. Proliferation - increase in number by mitoses/cell division
  3. Hypertrophy - increase in size
  4. Maturation
  5. Degeneration
  6. Calcification
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13
Q

Describe Diametric Growth in long bones

A
  • Miantained by periphysis
  • Ring of La Croix- Surroundig epiphysis
  • Zone of Ranvier - surroundign metaphysis.
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14
Q

What factors affect bone growth?

A
  • Mechanical/Local - s-ace - epiphysiodesis and epiphyseal distarction
  • Distractio osteosynthesis - Ilizarov
  • Systemic- Endocrine, Paracrine, autocrine
  • PTH-rP (parathyroid hormone related protein)
  • Indian hedgehog Ihh proetin
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15
Q

Membranous ossification - Describe the main steps

A
  • (Omit cartilage step)
  • Primtiive emsenchyme -> osteoprogenitor cells 0> osteoblasts
  • Lay down specialised collageb - osteoid
  • Calcify
  • Intramembranous ossification is the direct deposition of bone on thin layers ofconnective tissue and is characteristic of the bones on the top of the skull.
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16
Q

How do osteoclasts work with osteoblasts in th ebone remodelling cycle

A
  • Osteoclasts - form cutting cone reusltign in resorption bays destroying bone
  • Osteoblasts follow as closign cone laying new bone
  • Junction visible as a purple blue cement line
  • Constant renewal allows tensile strength to be retained
17
Q

Pleuripotent mesenchymal stem cells: What can they differentiate into?

A
18
Q

What are the 3 aetiotypes of frctures

A
  • Traumatic fracture- healthy or brittle bone
  • Stress/frsgility fracture - brittle bone wth low level or no trauma
  • Pathological fracture - health bone invovled by neoplastic pahtolgoical process - msot commonly secondary metastasis to bone or primary bone tumour - benign or malignant.
19
Q

What are thr 4 phases of fracture healing:

A
  • Haematoma formationa nd fracture healing
  • Organisation
  • Provisional callus formaiton
  • Defintiive callus and bony union
20
Q

Cement lines in bone

A

The cement line, which is the interface between the ‘fibers’ (osteons) and extraosteonal bone matrix, may impart important mechanical properties to compact bone.

21
Q

What are the 3 stages of fracture healing

A
  1. Inflammation (to) - haematoma + traumatic inflammation
  2. Repair (Within 2 weeks) - fibrous bridging if unopposed -> surfaces soft/provisional calludosteoid -> hard/definitive callus/spongy bone by mineralisation
  3. Remodelling - woven -> lamellated bone continues long after clinical healing
22
Q
A
23
Q

What does this image show

A

Provisional fracture callus, note zonation.

24
Q
A

Arche sof bone - periosteal reaction form inner cambium layer - benign

25
Q

Fractur ehealing - what type of bone changes are they?

A

Woven to lamellar bone (recapitulates otogeny ie, foetal boen growth)

CHodnrocytes/cartilage intemrediary involved only in displaced, unreduced fracture or where immobilisation is not fully ahcieved.

26
Q

in fractures - what tp we have to exclude as DDx?

A
  • Boen tumours. dx and D/D related ot anatomical site with respect to bone or speific bone and age (open or fused growth plate- skeletal maturity)
  • Osteomyelitis 0 inflammation of bone - acute or chronic - acute emergency
  • Nutritional deficiency disorders - Vit D def
  • Epiphyseal injuries and disorders, avascular necrosis
  • Non and malunion of fractures 0 neck of femur, scaphoid
  • Skeletal homeostasis
27
Q

Mechanism of osteoporisis

A
  • Inadequate bone deposition (maintainence), if developmental - osteopenia
  • And/or excessive bone resportion
  • Relative oestrogen deficiency in pre menopause
  • Absoloute oestrogen deficienct post- menopause
  • Central role of oestrogen in skeletla homeostasis and bone mineral density.
28
Q

Whata re the causes of osteoporosis

A
  • Vats majority - idiopathic, age related
  • Selected secondary causes 0 frequent, recent, current use of high dose long term systemic glucocorticoids
  • Endocrine blockage therapy for breast and prostate cancers.
29
Q

When to asses osteoporosis (NICE)

A
  • WOmen >65
  • Men >75
  • M 50-74, and F 50-64
  • History of falls
  • Fragility fracture
  • Very Low BMI
  • FH of hip fracture
  • High alcohol intake (>14 weekly units)
  • Long term high dose glucocorticoids
  • SMoking
30
Q

When do we assess the younger age group for osteoporosis

A
  • <50 steroid use, hisotry fragility fractures, premature meopause
  • <40 steroid use, multiple or major fragility fractures
  • >7.5mg glucocorticoids/day for ?3m
31
Q

WHo is at risk of osteoporosis

A
  • Geriatric age group -female dominence
  • Female athletes with amenorrhoea
  • immobialised patients
  • Breast + prostate cance ron endocrine blockagde
  • Rheumatoid arthritis ptient son long term steroids
  • Malabsorptive group - coeliacs, IBD, gastric bypass
  • Childhood cancer survivors
32
Q

How to assess for osteoporosis

A
  • FRAX/Q fracture risk algorithm without BMD (bone mineral density) using a DEXA scan- accuracy may be affected by previous vertebral or multiple fractures, high alcohol intake and glucocorticoids use
  • If in the intervention threshold- DEXA (dual energy X ray absorptiometry)
  • Lab investiagtions:
    • FBS, serum calcium, phosphorus, magnesium, ALP, creatinine
    • PTH, Vit D, TSH, testosterone
    • Selected clinical scenarios -Myeloma screen, hypecortisolism, maalbsroption, 24hours urinary calcium for malabsroption or idiopathic hypercalciuria.
33
Q

What is a DEXA score?

A

T scores- comparison of SD with young healthy cohort, 65 and M>75

Z score- compare with age matched healthy cohorts- useful for younger age group-

34
Q

Superimposed osteomalacia - what contributes to this

A
  • Vitamin D deficienc and Ca malabsoprtion
35
Q

How to prevent the risk of osteoorosis

A
  • Weight + strength training, physiotherpy
  • Smoking cessation and moderation in alcohol consumption
  • Prevention of falls - referral to falls services
  • Vit D: 800-1000IU/day with serumt arget value of ?30ng/ml calcium intake. 1000-1200mg - diet +/- supplement
36
Q

Pharacotherapy in Osteoporosis

A
  • Bisphosphontes -oral alendronate, risedronate iv - zolendronic acid, ibandronate
  • Endocrine therapy - human recombinant parathyroid homrone (teriparatide) - amino terminal of human PTH that binds to PTH1 receptor and recruits osteoblasts
  • Oestrogen replacement therpy
37
Q

Complications in osteoporosis

A
  • Daily bisphosphonates -heartburn, dysphagia - weekly better
  • Very rare- osteonecrosis of mandible
  • IV- flu like symptoms - no long term side effects
38
Q

Prognosis of osteopororsis

A
  • Untreated - 50% chance fracture following intiiating event
  • Treated - 40-70% reduction is spinal fracture nd 30-50% reduction in hip fracture