Term
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Definition
perichondrium consists of chondroblasts and chondrocytes
type II collagen
aggrecan proteoglycan
epiphyseal plates
can calcify
glassy
synovial (articular) joints
costal cartilage of rib cage
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Term
hyaline chondrogenesis and synovial joints |
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Definition
hyaline chondrogenesis usually takes place by appositional growth (cell on top of cell on top of cell)
this does not happen at synovial joints (the only exception for hyaline cartilage joints) because the chondroblasts would be work down by the constant activity of these joints
this is bad because there can be no regeneration of cartilage at these joints |
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Term
three matricies of interstitial carilage growth: |
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Definition
horizontal growth
capsular matrix around isogenous group
territorial matrix around capsular matrix
interterritorial matrix between isogenous groups |
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Term
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Definition
death of chondrocytes
decreased joint space -> erosion down to subchondral bone
signs:
heberdens nodes: osteophyte growth at DIP
bouchards nodes: osteophyte growth at PIP
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Term
features of elastic cartilage |
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Definition
flexiable and elastic
perichondrium consists of chondroblasts and chondrocytes
does NOT calcify
collagen type 2 and aggrecan
on epiglottis and larynx
marfans syndrome (walker "thumb" and steinberg "wrist" test) |
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Term
features of fibrocartilage |
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Definition
no perichondrium
can calcify
made of chondrocytes and fibroblasts
type 1 and 2 collagen
shock absorber
intervertebral discs |
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Term
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Definition
mass composed of concentric lamellae
Function
•Support and Structure
•Calcium and Phosphorus storage
•Detoxifcation of heavy metals
Lead Poisoning
Structure:
Endosteum - Inner lining of compact & spongy bone
Contains osteoprogenitor cells
Periosteum - Outer sheath of dense connective tissue (2 layers)
Outer Fibrous layer
Inner Osteogenic layer (contains osteoprogenitor cells) |
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Term
explain the haversian system |
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Definition
cylindrical concentric lamellae running vertically housing a canal within which blood vessels and nerves pass
volkmann's canals run horizontally but still carry vessels and nerves |
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Term
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Definition
they allow passages of substances between osteocytes and blood vessels (cell-cell communication) |
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Term
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Definition
¨Synthesize bone matrix proteins & collagen-I (osteoid)
¨ SecretingCells - Polygonal/cuboidal shape
¡ Prominent eccentric nucleus
¨ Inactive Cells - Flat, resemble osteoprogenitor cells
¡Usually lie in a single layer on growing edges of bone
different from osteocytes because blasts are surrounded by bone material and cytes are smaller, round or oval, and surrounded by a bone matrix |
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Term
where do osteoclasts originate from?
how are they activated? |
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Definition
macrophages
they are non-dividing and are NOT mesynchemal
the tiny pits and divits they cause in bone can be called howship's lacuna
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the precursor cell has a receptor which requires complexing with an RANK ligand (secreted by stromal cells and some osteoblasts) to become an osteoclast
osteoprotegrin (OPG) receptors are free floating and can bind RANK ligands so they are no longer available to bind to progenitor cell receptors. this is how bone destruction is prevented |
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Term
what is a hydroxyapatite? |
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Definition
it is a crystallized form of Calcium Apatite and can serve as a space filler in bone
it can be degraded by H+ ions |
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Term
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Definition
intramembranous ossification - the fusion of flat bones as in the skull bones
endochondral ossification - arises from mesenchymal stem cells which turn into progenitor cells, then osteoblasts, spicules, trabeculae, woven bone, then lamellar bone
Growth process:
1.Cartilage growth
2.Hypertrophy
3.Cartilage calcification
4.Reabsorption
5.Ossification |
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Term
Fractors regulating bone remodeling
actions of PTH and calcitonin
growth hormone
estrogen |
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Definition
PTH (parathyroid hormone) raises blood Ca2+ by stimulating osteoclasts, stimulates insteinal absorption of calcium, and inhibits kidney excretion
calcitonin inhibits PTH
growth hormone (GH) or somatotropin stimulate osteoprogenitor cells
IL-1, IL-6, TNF, and M-CSF promote osteoclast activity. estrogen inhibits them and therefore inhibits osteoclast activity. this is why osteoporosis can begin during menopause |
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Term
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Definition
FractureàTear of blood vesselsàBlood collectionàBlood clot
• Blood clot converted into granulation tissue (loose CT)
– Fibrocartilagefills the space forming aCallus
• Differentiation of osteoprogenitors in periosteum & endosteum
– Invade around & within callus
• Endochondral ossification of callus cartilage
• Spongy bone à Compact bone à Remodeled bone |
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Term
features of skeletal muscle |
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Definition
One cylindrical elongated cell (4-10cm, 10-100um diameter)
Polynucleated syncytium (work through gap junctions)
Peripheral nuclei (pushed aside by myofibrils)
Central myofibrils
◦Linear Sarcomeres
Cytoplasm = Sarcoplasm (rich in Glycogen)
Extensible cell membrane = Sarcolemma
Satellite cells = adult muscle stem cells (skeletal muscle)
◦Growth & Regeneration |
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Term
explain muscle fiber coverage |
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Definition
Epimysium
◦Outermost layer of connective tissue
◦Surrounds entire muscle
◦Synonymous with deep fascia
à Attachment & cushioning
Perimysium
◦Surrounds each muscle bundle (fasciculus)
◦Rich in capillaries
àPasses contractive force to periphery
Endomysium
◦Innermost layer of connective tissue
◦Surrounds each fiber
àHold muscle components together transmit contractive force houses blood vessels & nerves |
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Term
the sliding filament theory |
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Definition
actin/myosin sliding can actively contract, but the CANNOT actively extend (due to antagonis pairs). the release of calcium from troponin sites will naturally block myosin binding and the complex will will just relax |
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Term
what is Myasthenia Gravis
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Definition
an autoimmune disorder
eyelids droop and there is a weakening of the limbs (cranial nerves are most effected)
the patient has few ACh receptors, therefore, the action potential signal is not propogated very well. in order to strengthen the signal, an inhibitor of ACh esterases (the enzyme that clears ACh) can be introduced to increased the amount of ACh that is being delivered to muscle cells |
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Term
what is the difference between a repaired cell and an original myofiber? |
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Definition
the repaired cell will have a centrally located nucleus whereas the normal myfiber will have a eccentrically located nucleus |
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Term
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Definition
Striated
Branching
Mono or Bi-nucleated (centrally)
Muscarinic AChRà Atropine responsive
Electrically coupled à Syncytium
àIntercalated Disks (gap junctions)
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Term
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Definition
Lack of Striations, Central nucleus
Bladder, uterus, GI tract, respiratory tract, blood vessels, reproductive organs, ciliary muscle, pili of skin
Caveolae contain receptors for neurotransmitters, no NMJs
Autonomic nervous system (ANS) à Involuntary
Gap junctions
cytoskeleton: desmin, wimentin
contractile proteins: actin, myosin |
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Term
features of soft tissue tumors |
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Definition
slightly more frequent in the lower extremeties
more often benign
chromosomal abnormalites |
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Term
the most common adulthood soft tissue tumor and its features |
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Definition
lipoma, usually well encapsulated.
characteristic adiocytes will be present |
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Term
agressive types of liposarcoma and characterizing cell |
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Definition
round cell and pleomorphic liposarcomas are aggressive. you can tell it is a sarcoma and not a lipoma by the presence of lipoblasts
myxoid has an intermediate agressive nature |
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Term
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Definition
"reactive pseudosarcoma"
rapidily growing, appear on forearm often, sometimes following trauma
plump immature fibroblasts with a
"tissue culture growth" appearance |
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Term
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Definition
rare and malignant tumors often of the retroperitoneum, knee, thigh, distal peritoneum
radiation induced sarcomas
FISH FLESH (HERRINGBONE) type pattern is characteristic |
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Term
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Definition
a lesion, small and slow growing
SUPERFISCIAL
on palm: dupuytren contracture
also can be found on penis and plantar surface
composed of mature appear, but poorly defined fibroblasts; often myofibroblasts
DEEP
more rapidly growing, can be infiltrative
there are associations with mutations of the APC and beta-catenin genes
seen in Gardners Syndome (aka, FAP, famililial adenomatous polyposis) |
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Term
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Definition
(benign fibrous histiocytoma)
a slow growing nodule that can be infiltrative despite being benign
MAJOR CHARACTERISTIC: spindle cells in storiform (pin wheel) pattern
malignant counterpart to this would be a "malignant fibrohistiocytoma" |
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Term
what is the most common soft tissue tumor in children/adololescents? |
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Definition
rhabdomyosarcoma. often characterized by a t(2;13) where PAX3 is on chr. 2 and controls skeletal cell differentiation upsteam (this likely gets deregulated when it becomes juxtaposed to FKHR)
dx cell is the RHABDOMYOBLAST: tapdole cells, eccentric eosinophilic granular cytoplasm
variants include:
embryonal
alveolar (worst prognosis)
pleomorphic |
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Term
where might you find an embryonal rhabdomyosarcoma with the best prognosis? |
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Definition
in a hollow organ (ie. bladder, vagina). the subtume is "sarcoma botryoides" and it grows in a polypoid fashion resembling a cluter of grapes |
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Term
what is a malignant fibrohistiocytoma? |
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Definition
MHF, the most common sarcoma seen in adults. broken down into many subtypes, not just MHF.
Have pin-wheel appearance, sometimes bizarre appearing, multinucleated giant cells, IHC often needed for precise classifiication
frequent in lower extremities |
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Term
what is alveolar rhabdomyosarcoma? |
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Definition
a subtype of rhabdo which usually affects adolescents and carries the worst prognosis
found in the deep muscles of the extremities, it histologically takes on a crude appears of pulmonary alveloi |
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Term
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Definition
t(X;18)
Biphasic: two differentiaton layers
- epithelial: cuboidal to columnar and form glands
- spindle cells: arranged in dense, cellular fasciicles around the epithelial cells
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Term
effect of axonal degeneration of muscles? |
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Definition
denervation of muscles. when the neural input is lost, its is likely that the muscles will begin to atropy and the fibers will take on a triangular, angulated shape, become disorganized
neighboring unaffected nerve axons are capable of extending their branches to the denervated fibers to reinnervate them. The fibers will take on the metabolic features characteristic to that nerve, thereby losing that checkerboard appearance that is typically seen with a large mixtures of red and white fibers |
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Term
what is spinal muscular atrophy (SMA)? |
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Definition
and infantile disease associated with chr. 5
most common form is Wernig-Hoffman disease; limp baby; death by age 3
low muscles nervous stimulation leads to weak muscle tone all over
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Term
histological appearance of muscular dystrophy |
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Definition
- variations in fiber diameter
- degeneration, phagocytosis, necrosis of fibers
- evidence of some muscle cell regeneration
- later stages, muscles replaced by fat and connective tissue
since the diaphragm is a muscle, it is usually central to the ultimate cause of mortality
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Term
what is the method in which the DMD affected get up from the ground? |
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Definition
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Term
histology of mytonic dystrophy |
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Definition
selectivity to type I fibers
grip mytonia (cannot relax, have a sustained grip)
balding, cataracts, increased serum CPK |
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Term
what is malignant hyperthermia? |
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Definition
an ion-channel myopathy
they have a dramatic hypermetabolic state with tachycardia, tachypenea, muscles spasms, hyperpryexia |
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Term
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Definition
inflammatory disease of skin and skeletal muscle; capillaries are attacked by Abs and complement and lead to ischmia
symmetric weakness of proximal muscles first, slow onset with myalgia
later extramusclar involvement may include lung disease, vasculitis, and myocarditis
25% of patient have underlying cancer
Juvenile Dermatomyositis - also have GI symptoms, calcinosis is observed in 1/3 of cases
grottons scales, heliotrope rash on eyelids
POLYmyositis is same without skin involvement |
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Term
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Definition
like dermatomyositis but with no skin involvement
the inflammation is found in the endomysium
there is NO perifasicular atrophy or evidence of vascular damage
cell-mediated injury of myocytes |
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Term
why are nerve conductions studies in myasthenia gravis normal? |
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Definition
because there is no nerve pathology, there is receptor pathology. Abs to ACh receptors lead to loss of their fxn |
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Term
what do 65% of myasthenia gravis patients have? |
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Definition
thiymic hyperplasia. thyoma is present in 15% |
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Term
what is inclusion-body myostitis |
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Definition
skeletal muscle inflammation involving DISTAL muscles first and can be assymetric (in this was it is different from D/P)
rimmed vacuoles w/n myocytes are observed
unlike D/P, immunosupressives will not work as a therapy |
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