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R2
1. Describe the bone cells that are involved in the generation of bone tissue
Osteogenic cells are undifferentiated organisms from early-stage mesenchyme that lead
to most of the other bone cell types. Some of them mature into osteoblasts as they continue to
expand.
Osteoblasts are cells that form bones and support the mineralization of the natural parts
of bones. Osteogenesis is the process by which bones are formed. In the endosteum and inner
layer of the periosteum, osteoblasts form rows that resemble a cuboidal epithelium. Because they
are nonmitotic, the osteogenic cells are the only source of new osteoblasts. Stress and breaks
accelerate the mitosis of those cells, which causes an unexpected ascent in the number of
osteoblasts, which then, at that point, support or revamp the bone (Schlesinger et al., 2020).
Osteocytes serve a variety of purposes. Some add to the homeostatic support of bone
thickness and calcium and phosphate particle focuses in the blood by resorbing bone network
while others store it. Maybe significantly more critically, they are strain sensors. Sensory cilia on
osteocytes become active in response to stress, releasing signals that control bone remodelling,
Osteoclasts are cells that degrade bone on the surface of the bones. They originate from
the same stem cells found in blood cells and bone marrow. Osteocytes, osteoblasts, and
osteoblasts are examples of osteogenic cells. Osteoclasts differ from one another in many ways.
The osteoclast's side that is in contact with the bone's surface has a ruffled border due to
numerous deep plasma membrane infoldings that both increase the osteoclast's surface area and
R3
bone resorption efficiency. Resorption coves that osteoclasts scratch into the outer layer of the
1. Formation of hematoma: Following a break, veins inside the bone and encompassing
tissues burst, prompting the development of a hematoma (limited blood clump) at the crack site
(Howell et al., 2021). The hematoma serves as a temporary scaffold for the various processes of
subsequent repair.
hours of the fracture. The hematoma is invaded by inflammatory cells like neutrophils and
3. Formation of a callus: Within a few days, fibroblasts and osteoprogenitor cells relocate
to the break site, making a delicate granulation tissue called the callus (Sarah & Ardeshir, 2018).
The callus acts as a temporary bridge between the bone ends, stabilizing the fracture.
4. Callus ossification: Synthesizing new bone tissue is how osteoblasts inside the callus
bring about its ossification. The soft callus is converted into a hard, bony callus composed of
5. Bone remodelling: Over some time, there is remodelling in bony callus as a result of
which extra bones are dissolved by osteoclasts leading to restoring original shape and strength
(Bahney et al., 2018). Several months to years may be needed for this process, which depends on
2. The physician indicated that Kyndall was lucky because the fracture
occurred about 3 inches below the epiphyseal plate. Why is this important?
What are some possible outcomes if the epiphyseal plate had been damaged?
The epiphyseal plate or growth plate can be found close to both ends of long bones and is
responsible for their longitudinal development (Setiawati & Rahardjo, 2019). The location of
Kyndall's fracture about 3 inches beneath the crucial epiphyseal plate may impact her future bone
development. Epiphyseal plate damage might cause growth disruptions such as unequal limb
lengths or angular deformities. Rarely, premature closure of the epiphyseal plate may cause
The fracture, in my opinion, was a stress fracture. I think it was a fall that happened by
mistake because of something else. Samaila et al. (2021) notes that "stress fractures are caused
by abnormal traumas to a bone, such as fractures sustained in falls, athletic activities, vehicle
accidents, and military combat." This supports my side of the narrative since it demonstrates how
frequently accidents, namely falls, result in stress fractures. I think the stress fracture was
References
Bahney, C. S., Zondervan, R. L., Allison, P., Theologis, A., Ashley, J. W., Ahn, J., Miclau, T.,
Howell, M., Loera, S., Tickner, A., Maydick-Youngberg, D., Faust, E., Martin, S., Teleten, O.,
Bryant, R., Sandman, D., Greenstein, E., Bauer, K., Miles, J., Barsun, A., Schank, J.,
https://doi.org/10.25270/wmp.2021.2.1238
Sarah, A.-H., & Ardeshir, B. (2018). Soft and hard tissue repair. Scott-Brown’s
https://doi.org/10.1201/9780203731031-10
Schlesinger, P. H., Blair, H. C., Beer Stolz, D., Riazanski, V., Ray, E. C., Tourkova, I. L., &
https://doi.org/10.1152/ajpcell.00120.2019
Samaila, E., Colò, G., Rava, A., Negri, S., Valentini, R., Felli, L., & Magnan, B. (2021).
https://doi.org/10.1016/j.fas.2020.05.001
Setiawati, R., & Rahardjo, P. (2019). Bone Development and Growth. Osteogenesis and Bone
Regeneration. https://doi.org/10.5772/intechopen.82452