ROUNDS
RESPONSE.
Rounds is your vehicle for sharing your orthopaedic
skills and experience. Your response to Rounds will be published in
a future issue of Body Cast. We invite you to suggest questions for
this column. Please address all submissions to: The Editor, Body Cast,
18 Wynford Drive, Suite 715A, North York, Ontario, M3C 3S2.
This
Issue's Rounds Question -
Please tell
us:
What is topographical anticipation?
(responses
to be published in next issue)
In the last issue of Body Cast, Rounds asked:
How
is the repair of a fractured adult bone similar to endochondral
bone formation?
The following responses were received:
From Livain Arseneau:
Endochondral ossification is the process responsible for bone
growth in vertebrate skeletons, especially in long bones. Endochondral
ossification occurs by replacement of hyaline cartilage.
Successful fracture healing typically involves the production
of a cartilaginous callus, which is eventually remodelled into
new bone. The blood vessels in the advancing front of endochondral
ossification are likely to play an important role in the replacement
of cartilage within the callus.
From Lhea Burk:
Bones grow in length at the epiphyseal plate by a process that
is similar to endochondral ossification. The cartilage in the region
of the epiphyseal plate next to the epiphysis continues to grow
by mitosis. The chondrocytes next to the diaphysis age and degenerate.
Osteoblasts move in and ossify the matrix to form bone. This process
continues throughout childhood and adolescent years until the cartilage
growth slows and stops. When cartilage growth ceases, usually in
the early 20s, the epiphyseal plate completely ossifies so that
only a thin line remains and the bones can no longer grow in length.
From MaryAnne Lash:
When an adult fractures a bone, the repair or healing is similar
to endochondral bone formation. The similarity starts with the
process of endochondral ossification, which is
needed for skeletal development and bone repair. In development,
the cells differentiate into chondrocytes that produce a cartilage
matrix. This cartilage matrix produces osteoblasts. The osteoblasts
use calcified matrix as a pattern for the body to build bone. This
pattern is used in bone healing should a fracture occur. So, endochondral
ossification is how the body initially produces bone and later
uses the pattern to repair itself.
From Cheryl Rivers:
The similarity between the two is without endochondral ossification
there would be no bone formation. Endochondral ossification is
one of two types of bone formation and is the process responsible
for much of the growth in vertebrate skeletons, especially in long
bones. Endochondral ossification occurs by replacement of hyaline
cartilage. - Wikipedia Encyclopedia
From Heather Wong: Endochondral bone formation
Cause a proliferation and differentiating of stem cells (mesenchymal
cells) into chondroblasts that form cartilage and osteoblasts.
The production and maturation of cartilage and bone matrix. The
differentiation of circulating osteoclasts are precursor cells
into osteoclasts (remodelling cells).
Fracture healing
1. Reactive phase - fracture of bone and inflammation
• granulation
tissue forms
2. Reparative phase - callus forms
• bone
deposit
3. Remodelling - remodel to original bone contour.
From Neuville Yao:
During
the reparative phase of fracture repair, there's callus formation
and then there is lamellar bone deposition. This phase involves
the replacement of the hyaline cartilage and woven bone with "lamellar bone". The replacement process is known
as "endochondral ossification".
With
respect to the hyaline cartilage and "bony substitution" with
respect to the woven bone.
Substitution
of the woven bone with lamellar bone precedes the substitution
of the hyaline cartilage with lamellar bone. The lamellar bone
begins forming soon after the collagen matrix of either tissue
becomes mineralized. At this point, "vascular channels" with
many accompanying osteoblasts penetrate the mineralized matrix.
The osteoblasts form new lamellar bone upon the recently exposed
surface of the mineralized matrix. This new lamellar bone is in
the form of "trabecular bone". Eventually, all of the
woven bone and cartilage of the original fracture callus is replaced
by trabecular bone, restoring much, if not all, of the bone's original
strength.
From Thomas York:
In a fracture bone, osteoblasts, osteocytes and osteoclasts are
the three cell types involved in the development, growth and remodelling
of bones.
Osteoblasts are bone-forming cells. Osteocytes are mature bone
cells. Osteclasts break down and re-absorb bone.
Hyaline cartilage - somewhat elastic, semitransparent cartilage,
characterized by type 2 collagen and proteoglycan aggrecans. Seen
in movable joint surfaces and the physis (growth plate).
Endochondral ossification - involves the replacement of hyaline
cartilage with bony tissue. Bones are formed as hyaline cartilage
models. During the third month after conception, the perichondrium
that surrounds the hyaline cartilage models becomes infiltrated
with blood vessels and osteoblasts and changes into a periosteum.
The osteoblasts form a collar of compact bone around the diaphysis.
The cartilage in the centre of the diaphysis begins to disintegrate.
Osteoblasts penetrate the disintegrating cartilage and replace
it with spongy bone. This forms a primary ossification centre.
Ossification continues from this centre toward the ends of the
bone. After spongy bone is formed in the diaphysis, osteoclasts
break down the newly formed bone to open the medullary canal.
The cartilage in the epiphysis continues to grow so the developing
bone increases in length. Ossification in the epiphysis is similar
to that in the diaphysis except that the spongy bone is retained
instead of being broken down to form the medullary cavity.
Responses
were also received from: B. Arseneault, J. Carragher,
E. Christiansen, A. Crossman, R. Grenier, C. Griffith,
S. Groulx, L. Head, B. Lavallee, N. Lockyer, C. Longphee,
D. Longphee, L. Lough, L. MacDonald, B. Matheson,
J. Maulucci, G. Marshall, E. Oborowsky, R. Passmore,
J. Pike, J. Punwassie, B. Sheppard, A. Tarambikos
and A. Wentzell.
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