chap 21 - disorders of the bones and joints Flashcards
skeletal system function
reservoir of minerals (calcium and phosphorus), protection, production of blood cells, movement, shape, rigid support
structure of skeletal system
bone is connective tissue, all bones have the same basic structure - cortex, trabeculae, and bone marrow
cortex
outlayer of compact bone
trabeculae
inner spongy layer of the bone
bone marrow
spaces between trabeculae consist of fat and blood-forming tissue
bone
dynamic living tissue, undergoing remodeling
- strength and thickness depend on activity
bone cells
osteoclasts, osteoclasts, osteocytes
bone growth
ossification
types: endochondral and intramembranous
endochondral ossification
lay down cartilage, laying down of bone, ossification at epiphyseal plate
intramembranous ossification
no cartilage phase occurs, typically occurs in flat bones
bone density
- amount of mineral per cm/bone
- indicator of fracture risk
factors influencing bone mineral density
diet(calcium, vitamin D, K+, magnesium,protein) , physical activity, hormones (calcitonin, parathyroid hormone, estrogen), age, sex
signs and symptoms
pain, decreased mobility, deformity
symptoms associated with arthritis
joint stiffness and decreased mobility
tests
diagnostic modalities
- radiography to visualize fractures and bony abnormalities
osteoblasts
secrete the matrix that will help build the bones
b = build
osteoclasts
ruffled membrane, causes bone resorption which is breaking down bone
osteocytes
cell of the bone, embedded in the matrix of the bone
osteoprogenitor
can become any bone cell
erythrocyte sedimentation rate
How long does it take for red blood cells to settle in a sample - shows systemic inflammation, increase in systemic inflammation causes the cells to be stickier and settle first, increase of erythrocyte settlement rate (could show arthritis because inflammation is one of the main manifestations of arthritis)
achondroplasia
- Plasia = division, chon = cartilage, chondrocytes, a=no → without chondrocyte dividing, important for bone formation, no laying down of cartilage, no laying down of bone
Leading cause of dwarfism
Causes mutation in fibroblast growth factor 3 (FGFR3) - Autosomal dominant
- Majority de novo mutations, de novo = new
- Most common risk is age of the father
Result in Faulty bone formation
Impaired growth of extremities and formation of skull bones
- Most common risk is age of the father
- Can lead to stenosis on the spinal cord due to malformation of foramen magnum in occipital bone
Causes dwarfism with disproportionately short limbs
osteogenesis imperfecta
“Brittle Bone” Disease = Thin and delicate bones easily broken
“Imperfect bone formation”
Mutation in genes resulting in abnormal collagen formation
- Collagen is of normal quality but is produced in insufficient quantities
- Collagen is part of the cartilage that is laid down prior to the bone
Autosomal Dominant
Increase susceptibility to bone fractures
May be in utero
Eight Types
- I-VIII
- Different types of collagen
Malformation of fingers and toes
Spinal curvature
Brittle teeth
Blue Sclera - thin because it is a connective tissue disorder and the sclera is connective tissue, so the veins are showing through
congenital clubfoot (talipes)
The most common congenital disorder of the legs
Not painful
Multifactorial inheritance - environment and genetic susceptibility
Treatment: manipulation and casts
fractures
Any disruption in continuity of bone
Most often caused by
Trauma
Pathologic fracture
Underlying disease of bone
Pain resulting from tearing of periosteum (covering of the bone)
- types: simple, comminuted, compound, pathologic, and greenstick
in order for a fracture to heal
- broken fragments must be close to each other, also must be stabilized
healing process: involves proliferation of
- osteoblasts from fracture margins - lay down new matrix which will be mineralized to make new bone, vascular channels from periosteum
- immature bone and cartilage gradually remodel into mature bone