Metabolic bone disease: histopathology Flashcards
Functions of bone: • STRUCTURE – • MECHANICAL – • PROTECTIVE – • METABOLIC –
• STRUCTURE – give structure and shape to the body • MECHANICAL – sites for muscle attachment • PROTECTIVE – vital organs and bone marrow • METABOLIC – reserve of calcium and other mineral
The composition of bone
• INORGANIC -65% –
• ORGANIC -35% –
- INORGANIC -65% – calcium hydroxyapatite (Ca10(PO4)6(OH)2) – is storehouse for 99% of Calcium in the body – 85% of the Phosphorus, 65% Sodium, Magnesium
- ORGANIC -35% – bone cells and protein matrix
bone geography
look at the bones and label
what are the bone types/classifications?
• 3 types
• describe each one
• Anatomical bones
-Flat, long, short/cuboid, irregular, sesamoid
• Macroscopic structure – trabecular/cancellous/spongy – cortical/compact
• Microscopic structure – Woven bone (immature) – Lamellar bone (mature)
what are the two classification of bones?
CORTICAL • long bones • 80% of skeleton • appendicular • 80-90% calcified • mainly structural, mechanical, and protective
CANCELLOUS • vertebrae & pelvis • 20% of skeleton • axial • 15-25% calcified • mainly metabolic • large surface area
learn cortical bone microanatomy
see slides
Name three types of bone cells and what they do:
- Osteoclasts - multinuclear cells that resorb/remove bone
- Osteoblasts - produce osteoid to form new bone
- Osteocytes - mechanosensory network embedded in mature bon
why perform a bone biopsy?
- Confirm the diagnosis of a bone disorder
- Find the cause of or evaluate ongoing bone pain or tenderness
- Investigate an abnormality seen on X-ray
- For bone tumour diagnosis (benign vs malignant)
- To determine the cause of an unexplained infection
- To evaluate therapy performance
what are the types of bone biopsy?
- Closed – needle -core biopsy (Jamshidineedle)
* Open –for sclerotic / inaccessible lesion
what are the histological stains?
- H & E
- Masson -Goldner Trichrome
- Tetracycline/Calceinlabellin
what is metabolic bone disease?
What is it due to?
What does it cause?
A group of diseases that cause reduced bone mass and reduced bone strength
• Due to imbalance of various chemicals in the body (vitamins, hormones, minerals, etc)
• Cause altered bone cell activity, rate of mineralisation, or changes in bone structure
Give some examples of common metabolic bone disease:
- Osteoporosis
- Osteomalacia/Rickets • Primary hyperparathyroidism
- Renal osteodystrophy
- Paget’s disease
Define osteoporosis
Two types
- Defined as a bone mineral density T-score of -2.5 or lower – Standard deviations different from mean peak bone mass BMD
- 1º -age, post-menopause • 2º -drugs, systemic disease
- High turnover vs low turnover
what is osteomalacia?
What are the two types?
- Defective mineralisation of normally synthesized bone matrix
- Rickets in children
- Effectively 2 types – Deficiency of vitamin D – Deficiency of PO
Osteomalacia-Sequelae
Osteomalacia-Sequelae
• bone pain/tenderness • fracture • proximal weakness • bone deformity
what is hyperparathyroidism
Excess PTH • increased Ca + PO4 excretion in urine • hypercalcaemia • hypophosphatemia • skeletal changes of osteitis fibrosa cystica
Which 4 organs are directly affected in hyperparathyroidism?
• 4 organs are directly or indirectly affected by PTH and between them control Calcium metabolism • Parathyroid glands • Bones • Kidneys • Proximal small intestine
What is primary and secondary hyperparathyroidism caused by?
- 1º – parathyroid adenoma (85-90%) – chief cell hyperplasia
* 2º – chronic renal deficiency – vit D deficiency
Symptoms for hyperparathyroidism
- Stones (Ca oxalate renal stones)
- Bones (osteitis fibrosa cystica, bone resorption)
- Abdominal groans (acute pancreatitis)
- Psychic moans (psychosis & depression
What does renal osteodystrophy do?
Comprises all the skeletal changes resulting from chronic renal disease:
– Increased bone resorption (osteitis fibrosa cystica)
– Osteomalacia
– Osteosclerosis
– Growth retardation
– Osteoporosis
What is paget’s disease?
Disorder of bone turnover
what are the three stages of paget’s disease?
Divided into 3 stages
- Osteolytic
- Osteolytic-osteosclerotic
- Quiescent osteosclerotic
Epidemiology of paget’s disease
Onset > 40y (affects 3-8% Caucasians > 55y) M>F
Rare in Asians and Africans Mono-ostotic15%
Remainder polyostoti
Aetiology of Paget’s disease
Aetiology is unknown Familial cases show autosomal pattern of inheritance with incomplete penetrance (mutations in SQSTM1 or RANK) Parvomyxovirustype particles have been seen on EM in Pageticbone –some doubt this is cause. Overuse or previous bone injury
clinical symptoms of paget’s disease
pain – microfractures – nerve compression (incl. Spinal N and cord) – skull changes may put medulla at risk – deafness – +/-haemodynamic changes, cardiac failure – hypercalcaemia – Development of sarcoma in area of involvement 1