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196 Cards in this Set
- Front
- Back
functions of bone
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support
protection movement blood cell formation mineral homeostasis |
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types of bone cells
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osteoblasts
osteoclasts osteocytes |
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primary function of osteoblasts
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to form new bone
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Synthesizes collagen and proteoglycans; stimulate osteoclast resorptive activity
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osteoblasts
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main bone matrix (maintenance)
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osteocytes
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Resorb bone, assist with mineral homeostasis
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osteoclasts
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marrow cavities where bone marrow is made in adults
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skull, vertebrae, ribs, sternum, shoulders and pelvis
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Irregular, scalloped cavities created by osteoclasts
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Howship lucunae or resorption bays
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Area of the cell membrane that forms infoldings to permit intimate contact with the resorption bay, greatly increasing surface area
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the ruffled boarder
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osteocytes bind to the bone surface through attachments called
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integrines
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derived from mesenchymal cells and produce type I collagen
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osteoblasts
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Responsive to parathyroid hormone and produce osteocalcin when stimulated
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osteoblasts
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Bone is shapped according to its function
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Wolff's Law
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Both an active and resting state. Is termed osteoid when active and termed satellite cells when active
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osteoblasts
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found in the lacuna of the bone matrix, most numerous bone cells
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Osteocytes
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Maintains bone matrix by making new bone matrix molecules, assisting in calcification and concentrating nutrients in the matrix
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osteocytes
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What does osteoclasts secrete in order resorb bone
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HCI and proteinases and use lysosomes
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allows osteoclasts to bind to bone surface
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integrines
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synthesizes collagen and proeoglycans; stimulate osteoclast resorptive activity
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osteoblasts
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maintains bone matrix
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osteocytes
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resorb bone; assists with mineral homeostasis
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osteoclasts
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are essentially osteoblast trapped in lacuna
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osteocytes
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matrix of bone that is nonmineralized
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osteoid
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assist osteocytes in calcification and mineral homeostasis. preparation for remodeling. help concentrate nutrients in the matrix. help with bone calcification
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osteocytes
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assist osteocytes in calcification and mineral homeostasis. preparation for remodeling. help concentrate nutrients in the matrix. help with bone calcification
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osteocytes
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assist osteocytes in calcification and mineral homeostasis. preparation for remodeling. help concentrate nutrients in the matrix. help with bone calcification
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osteocytes
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assist osteocytes in calcification and mineral homeostasis. preparation for remodeling. help concentrate nutrients in the matrix. help with bone calcification
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osteocytes
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types of bone tissue
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compact (cortical)
spongy (cancellous) |
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The basic structural unit is the haversian system that consists of
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Central canal called the haversian canal
Circular layers of bone matrix called lamellae Tiny spaces between the lamellae called lacunae Bone cells within the lacunae called osteocytes Small channels or canals called canaliculi |
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Less complex and lacks haversian systems
Lamellae are arranged in plates or bars called trabeculae irregular meshwork; pattern of the meshwork is determine by the stress on that particular bone red bone marrow |
Spongy (cancellous) bone
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double-layered connective tissue that covers all bones
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Periosteum
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Rips and scapula
2 plates of compact bone that are roughly parallel to one another; between the 2 plates is a layer of spongy bone |
Flat
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Wrist and ankle bones; cuboidal
Consist of spongy bone covered by a thin layer of compact bone |
Short
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Vertebrae, mandibles and other facial bones
Various shapes that include thick and thin segments The thin part consists of 2 plates of compact bone with spongy bone in between The thick part consists of spongy bone surrounded by a layer of |
Irregular
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three phase process where existing bone is resorbed and new bone is laid down to replace it
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Remodeling
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made up of bone precursor cells that later become osteoclasts or osteoblasts
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Basic multicellular units
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takes about 3-4 months, is an isolated process
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Remodeling process
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Remodeling process: Activation
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a stimulus (hormone, drug, vitamin or physical stressor) activates the bone cell precursors to form osteoclasts
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Remodeling process: Resorption
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osteoclasts form “cutting cone,” which gradually resorbs bone, leaving behind a resorption cavity *Resorption cavities in compact bone follow the longitudinal axis of the haversian systems; resorption cavities in spongy bone parallel the surface of the trabeculae
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Remodeling process: Formation
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the laying down of new bone (secondary bone) by osteoblasts lining the walls of the resorption cavity.
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Bone repair process: (spongy bone heals faster)
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Inflammation/hematoma formation (within hours)
Procallus formation (within days) Callus formation (within weeks) Replacement, by basic multicellular units (within years) of the periosteum and endosteum to the size and shape of the bone before the injury (up to 4 years) |
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The site where 2 or more bones are attached is called a
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joint, or articulation
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Types of joints
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fibrous, cartilaginous or synovial
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Synarthrosis =
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immovable
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thin layer of dense fibrous tissue that binds together flat bones in the skulls of young children, they form an extremely tight union that permits no motion. By adulthood, the fibrous tissue has been replaced by bone
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Sutures
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joint in which 2 bony surfaces are united by a ligament; ligament fibers are flexible and allow a limited amount of movement. Examples of syndesmotic joints are the paired bones of the lower arm (radius/ulna) and the lower leg (tibia/fibula)
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Syndesmoses
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a cone-like projection fits into a complementary socket and is held there by a ligament. The teeth held in the maxilla or mandible are gomphosis joints
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Gomphoses
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Amphiarthrosis =
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slightly movable
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: a joint where bones are united by a pad or disk of fibrocartilage; usually a thin layer of hyaline cartilage covers the articulating surfaces and a thick pad of fibrocartilage acts as a shock absorber and stabilizer. Examples are the pubic symphysis and the intervertebral disks
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Symphysis:
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a joint where hyaline cartilage (no fibrocartilage) connects 2 bones. An example is the joints between the ribs and sternum- slight movement allows the chest to move during breathing. The hyaline cartilage is called costal cartilage
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Synchondrosis
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Diarthrosis =
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freely movable
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surround by a membrane capable of excitation and impulse propagation
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Muscle fibers
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elongated muscles shaped like straps and can run from one joint to another
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Fusiform muscles:
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broad, flat and slightly fan-shaped with fibers running obliquely to the muscle’s long axis
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Pennate muscles
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Skeletal muscle can be either
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either voluntary (controlled by nervous system), striated (striped pattern) or extrafusal (to distinguish from other contractile fibers in the sensory organ of the muscle).
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2 types of sensory receptors in muscles:
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muscle spindles and Golgi tendon organs
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are mechanoreceptors that lie parallel to muscle fibers and respond to muscle stretching.
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Spindles
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are dendrites that terminate and branch to tendons near the neuromuscular junction.
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Golgi tendon organs
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sensory receptors in muscles are responsible for
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the muscle stretch response and maintenance of muscle tone.
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A motor unit consists of
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(1) anterior horn cells (2) its axon and (3) the muscles innervated by it.
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units consist of one motor neuron innervating many muscle fibers. They fatigue slowly and have endurance. They are used for large, powerful movements because of their high innervation ratio of muscle fibers to axons
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Large motor units
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units have one motor neuron innervating a few muscle fibers (1 to 10). They fatigue quickly and have low endurance. Their low innervation ratio makes them capable of fine movements that require precision
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Small motor units
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Each muscle fiber contains bundles of
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myofibrils
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composed of myofilaments; the most abundant sub-cellular muscle component (make up 85%-90% of total volume)
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Myofibrils
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Muscle fibers develop from precursor cells called __________, the main cells responsible for muscle growth and regeneration. They are termed satellite cells when inactive.
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myoblasts
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2 types of muscle fibers:
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(1) Type I fibers (slow twitch)
(2) Type II fibers (white fast-motor) |
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Muscle membrane has 2 parts:
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sarcolemma (plasma membrane) and basement membrane
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capable of propagating electrical impulses to initiate contraction; it is made up of lipids and proteins.
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sarcolemma
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cytoplasm of the muscle cell and contains intracellular components – provides a matrix that surrounds the myofibrils.
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Sarcoplasm
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network that crosses the interior of the cell that’s primary function is calcium transport, which initiates sarcomere contraction
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Sarcoplasmic reticulum
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Sarcomere: make up myofibrils; they are composed of 2 contractile proteins called
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actin (thin filament) and myosin (thick filament)
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houses enzymes used in energy production, especially those that regulate the citric acid cycle and ATP formation
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Mitochondria
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Steps in skeletal muscle contractions
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(1) excitation (2) coupling (3) contraction and (4) relaxation
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At rest, an electric charge of ____ is continually maintained across the sarcolemma.
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-90V
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Follow depolarization of transverse tubules
Triggers release of Ca ions from S.R., which exposes binding sites on the actin molecule Troponin and tropomyosin (which bind to actin at rest) are attracted to Ca, leaving actin free to bind with myosin |
Coupling
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Begins with spread of an action potential from nerve terminal to neuromuscular junction
Rapid depolarization of membrane = muscle fiber action potential (electric impulse in muscle fiber membrane) Action potential spreads to transverse tubules as it travels across the sarcolemma |
Excitation
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Begins as Ca ions combine with troponin
Myosin binds to actin forming cross-bridges Myosin heads attach to actin-binding sites, pulling the actin (thin filament) inward Thin filament (actin) slides toward the thick filament (myosin) cross-bridge called the actin-myosin complex |
Contraction
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Begins as Ca ions are actively transported back into the S.R., removing ions from interaction with troponin
Cross-bridges detach and the sarcomere lengthens |
Relaxation
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Skeletal muscle requires a constant supply of
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ATP and phosphocreatine
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ATP → ADP + Pi (? seconds)
Phosphocreatine + ADP → creatine + ATP (~? seconds) Anaerobic glycolysis → lactic acid + ATP (~? seconds) |
ATP → ADP + Pi (2-3 seconds)
Phosphocreatine + ADP → creatine + ATP (~10 seconds) Anaerobic glycolysis → lactic acid + ATP (~90 seconds) |
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With increased activity (intense exercise or ischemia- inadequate blood supply due to blocked vessels), an increase in lactic acid occurs due to the breakdown of glycogen- causes shift in muscle pH
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Anaerobic (short-term) glycolysis
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Activated by strenuous exercise, which requires oxygen
Takes longer to make ATP Requires oxygen to (1) maintain maximal activity and (2) return the muscle to its resting state |
Aerobic (long-term) glycolysis
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accumulated by sustaining maximal muscular activity, it is the amount of oxygen needed to oxidize residual lactic acid, convert it to glycogen and replenish ATP and phosphocreatine stores
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Oxygen debt
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Type II muscle
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Type II muscle fibers rely on anaerobic glycolysis and fatigue readily.
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Type I fibers
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Type I fibers can resist fatigue longer because of their capacity for oxidative metabolism.
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Type of muscle contraction
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Isometric, Isotonic, Agonist and antagonist muscles
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Muscle maintains a constant length as tension is increased
Example: when the arm or leg is pushed against an immovable object. The muscle contracts but the limb does not move Also called a static (holding) contraction |
Isometric
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Muscle maintains a constant tension as it moves
Eccentric (lengthening): the muscle lengthens and absorbs energy. Negative work is accomplished on the muscle by the load. It requires less energy and has been said to result in the development of pain and stiffness after unaccustomed exercise Concentric (shortening): accomplishes positive work and energy is used to exert force or lift an object |
Isotonic
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Muscles don’t act alone, they act in groups!!!
Agonist: when a muscle contracts and acts as a prime mover Antagonist: the reciprocal muscle to the agonist that relaxes Happens automatically Their primary function is to maintain balance |
Agonist and antagonist muscles
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age-related loss in skeletal muscle which also causes decreased muscle strength- thought to be secondary to progressive neuromuscular changes and diminishing anabolic hormones (different than osteopenia, which is lowered density of bone minerals)
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Sarcopenia
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Decline in muscle proteins related to declines in
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insulin-like growth factor 1, testosterone and DHEA-sulfate
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Skin not broken; non-communicating wound between bone & skin
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Closed
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Skin broken; communicating wound between bone & skin
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Open
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Bone breaks into 2 or more fragments
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Comminuted
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Runs parallel to the long axis of the bone
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Linear
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Occurs at an oblique angle to the long axis (bone shaft)
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Oblique
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Encircles the bone (spiral staircase)
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Spiral
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Occurs straight across the bone
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Transverse
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Fragments pushed into each other
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Impacted
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Break at the site of a preexisting abnormality
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Pathologic
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Perforates one cortex and splinters the spongy bone ( outer surface disrupted, inner surface intact); commonly occurs in the proximal metaphysis or diaphysis of the tibia, radius and ulna in children and elderly
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Greenstick
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Cortex buckles but doesn’t break
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Torus
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Bending of the bone due to longitudinal stress; common in children and usually seen in the radius-ulna or tibia-fibula and difficult to treat (complete fracture in one bone and incomplete in the other)
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Bowing
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(1) fatigue fractures seen in people who engage in unfamiliar, strenuous and repetitive activity (athletes whose muscles develop too quickly) and (2) insufficiency fractures due to bone’s inability to deform and recover (rheumatoid arthritis, Paget disease, osteomalacia and radiation therapy)
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Stress
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Separation of articular cartilage from bone shaft; commonly occur in the distal femur, ankle, kneecap, elbow and wrist and are most prevalent in adolescents
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Transchondral
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Bone break- occurs from the damaged ends of bone and neighboring soft tissue
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Bleeding
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Bone break- forms within the medullary canal between the fractured ends and beneath the periosteum
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Clot or hematoma
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The temporary displacement of one or more bones in a joint in which the opposing bone surfaces lose contact entirely
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Dislocation
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When the contact between opposing bone surfaces is only partially lost; both dislocation and subluxation common in people younger than 20 and are associated with fractures- joints most often dislocated or subluxated are the synovial joints
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Subluxation
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A tear in a tendon; most common in the hands & feet, knee (patellar), upper arm (biceps and triceps), thigh (quadriceps), ankle and heel (Achilles)
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Strain
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A tear in a ligament; most common in the wrist, ankle, elbow and knee joints
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Sprains
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Complete separation of a tendon or ligament from its bone; commonly seen in young athletes (especially track)
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Avulsion
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Tendon inflammation, also called tendinopathy
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Tendonitis
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Inflammation of a tendon where it attaches to a bone, (1) Lateral- “tennis elbow” and (2) Medial- “golfer’s elbow”
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Epicondylitis
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Inflammation of the bursae, or small sacs lined with synovial membrane and filled with synovial fluid that are located between tendons, muscles and bony projections
Their primary function is to separate, lubricate and cushion Caused by trauma or wound infection (septic bursitis) |
Bursitis
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Local muscle damage that is a mild injury most often seen after traumatic or sports injuries
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Muscle strain
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Late complication of muscle injury thought to be caused by scar tissue calcification and ossification; “rider’s bone” or “drill bone”
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Myositis ossificans
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Life-threatening complication of severe muscle trauma, can lead to renal failure or shock
Detected by an excess of myoglobulin (intracellular muscle protein) in the urine, resulting in dark red to brown urine Caused by trauma, malignant hyperthermia, drug overdose, tetanus, heat stroke, fractures, etc. Most severe form called crush syndrome; less severe and more localized forms called component syndromes (Volkmann) Myoglobulin released when there are holes in the sarcolemma |
Myoglobinuria or
“rhabdomyolysis (Breakdown of muscle cells) |
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“porous bone”- most common bone disease
Old bone resorbed faster than new bone is made |
Osteoporosis
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Postmenopausal osteoporosis: attributed
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estrogen deficiency
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hunchback due to vertebral collapse
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Kyphosis
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Inadequate & delayed mineralization of osteoid in mature compact and spongy bone
Remodeling cycle proceeds normally through osteoid formation but mineral calcification & deposition don’t occur Primarily caused by a vitamin D deficiency (vitamin D helps the body absorb Ca) Causes skeletal pain and tenderness, especially in the hips so the person has trouble walking; waddling gait |
Osteomalacia
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Bone mass decreases
No pain |
Osteoporosis
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Soft bone instead of hard bone; volume unchanged
Pain and gait change |
Osteomalacia
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osteitis deformans
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Paget disease
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State of increased metabolic activity in bone characterized by abnormal and excessive bone remodeling- both resorption and formation!
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Paget disease
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“bone infection”
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Osteomyelitis
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Most often caused by bacteria and is very difficult to treat
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Osteomyelitis
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caused by pathogens carried in the blood from sites of infection elsewhere in the body and spreads from bone to adjacent soft tissues, usually caused by Staphylococcus aureus
Common complication of sickle cell anemia and low oxygen tension |
Osteomyelitis Endogenous
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infection that enters from outside the body (through open fractures, wounds or surgical procedures) and spreads from soft tissues into the adjacent bone
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Osteomyelitis Exogenous
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area of devitalized bone
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Sequestrum
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layer new bone surrounding infected bone
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Involucrum
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Degenerative synovial joint disease- loss and damage of articular cartilage in load-bearing areas
(1) absence of synovial membrane inflammation (2) lack of signs & symptoms (3) normal synovial fluid |
Osteoarthritis
(Noninflammatory) |
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Osteophytes
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bone spurs that occur due to the disease
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Inflammatory damage/destruction in the synovial membrane or articular cartilage
Fever, leukocytosis, malaise (uneasiness), anorexia, lymph node/spleen enlargement, Raynaud phenomeno |
Inflammatory joint disease “arthritis”
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Autoimmune disease associated with swelling and pain in multiple joints. Attacks (1) synovial membrane (2) articular cartilage (3) tendons & ligaments Results in destruction and instability of synovial joints!!!
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Rheumatoid arthritis (RA)
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swellings in areas of pressure or trauma that are found in 20% of RA cases
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Rheumatoid nodules
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caused by pulmonary nodules and chronic inflammation of the lungs
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Caplan syndrome
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Chronic, inflammatory joint disease characterized by stiffening and fushion (ankylosis) of the spine and sacral joints (cartilaginous joints!!!) Different than RA in that the primary site of inflammation is the enthesis whereas in RA the primary site of inflammation is the synovial membrane
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Ankylosing spondylitis (AS)
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Desmophyte
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new enthesis made by osteoblasts that forms on top of the old one
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small, white nodules that form in subcutaneous tissues
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Tophi
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-70mV. Delayed relaxation after voluntary muscle contraction
Distinct “dive bomber” noise caused by prolonged depolarization of the muscle membrane. Result of ion channel dysfunction Treated with drugs that reduce muscle fiber excitability |
Myotonia
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Episodes of flaccid weakness that typically lasts a few hours
Autosomal dominant inheritance!!! During an attack, the muscle membrane is unresponsive to neural stimuli and the resting membrane potential is reduced from -90V to -45mV. Caused by potassium, chloride or sodium channel abnormalities |
Periodic paralysis
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primary functions of skin
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(1) protect the body from the environment by serving as a barrier against microorganisms, UV rays, loss of body fluids and the stress of mechanical forces (2) regulate body temperature (3) regulate the immune system (4) activate/produce vitamin D (5) produce sensation and (6) provide psychological well-being
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Contains kerotinocytes, melanocytes and Langerhans cells
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Epidermis
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Papillary layer (thin): contains mast cells and has a rich blood, lymphatic & nerve supply. It contains sensory receptors and special glands
Reticular layer (thick): contains histiocytes, which are wandering macrophages that collect pigments and inflammatory debris |
Dermis
“true skin” |
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Underlying layer of connective tissue that contains macrophages, fibroblasts and fat cells
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Hypodermis
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an open comedone with a dilated orifice
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blackhead
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a closed comedone with a narrow head
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closed
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Burrow
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Narrow, raised, irregular channel caused by a parasite
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Circumscribed area of blood less than 0.5 cm in diameter
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Petechiae
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ulcers or pressure sores that develop when an individual lies in the recumbent position for a long term
Usually develop over bony prominences |
Decubitus ulcer
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Circumscribed area of blood greater than 0.5 cm in diameter
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Purpura
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Dilated, superficial blood vessels
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Telangiectasia
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sharply elevated, irregular or claw shaped, progressively enlarging scars caused by excessive amounts of collagen. Claw-like prolongations are typical
Tend to run in families |
Keloids
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Pruritus
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itching caused by skin disorders
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Pruritus stimuli Inflammatory substances:
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histamine, prostaglandin, bradykinin
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Pruritus stimuli neuropeptides and neurotransmitters
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serotonin, substance P, acetylcholine
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2 most common inflammatory disorders
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A.) Eczema
B.) Dermatitis |
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Langerhans cells process the antigen/allergen and carry it to the T cells. The T cells then become sensitized to it which induces the release of cytokines and dermatitis symptoms cell-mediated or delayed hypersensitivity
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Allergic contact dermatitis (exogenous)
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non-immunologically mediated inflammation. Severity related to the concentration of the irritant and exposure time
Caused by chemical irritation (acids) or prolonged exposure to soaps, detergents and various other agents used in industry which all can cause inflammatory lesions |
Irritant contact dermatitis (exogenous)
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More common in infancy and childhood but may persist into adulthood
Infected people show an increased IgE , interleukin-4 and eosinophil levels Skin becomes very dry, itchy, sensitive and easily irritated because the barrier function of the skin is impaired Associated with allergic rhinitis/asthma |
Atopic dermatitis (endogenous)
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Usually occurs on the legs as the result of venous stasis and edema
Associated with varicosities, phlebitis and vascular trauma. Alleviated by not wearing tight clothes around the legs and not standing for long periods, can be treated with antibiotics, wet dressings of Burrow solution or silver nitrate |
Stasis dermatitis (endogenous)
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Known as cradle cap in infants
Cause is unknown but Malassezia yeasts have been implicated |
Seborrheic dermatitis (endogenous)
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Chronic, relapsing. Types include plaque, inverse, guttate, pustular and erythrodermic. The turnover time to shedding the epidermis quickens to 3-4 days. Loosely cohesive, immature keratin gives lesions a silvery appearance
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Psoriasis
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occurs during winter. Begins as a single lesion called a herald patch on the trunk of the body that is circular, salmon-pink and 3-4 cm in size. Small erythematosus papules enlarge into oval lesions- form pattern of a drooping pine tree
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Pityriasis rosea
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Benign autoimmune inflammatory disease of the skin & mucous membranes. Triggered by drug use or film processing chemicals. Often in oral mucous membranes that appear as lacy, white rings. May be caused by an abnormal T-cell mediated immune response
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Lichen planus
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Disorder of the pilosebaceous follicle that usually occurs during adolescence.Noninflammatory: blackheads and whiteheads
Inflammatory: closed comedones with follicular wall rupture and sebum in the dermis causes inflammation |
Acne vulgaris
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Middle age or adult onset. Accompanied by eye disorders and rhinophyma (bulbous nose) from hypertrophy of sebaceous glands
Avoid hot drinks or alcohol Idiopathic |
Acne rosacea
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Autoimmune systemic inflammatory disease that expresses cutaneous manifestations. Discoid (cutaneous): limited to the skin and can lead to systemic.“butterfly rash”. May lead to alopecia (hair loss), urticaria, telangiectasias or Raynaud phenomenon.
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Lupus erythematosus
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both vesiculobullous disorders causing vesicles or blisters
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pemphigus and erythema multiforme
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Rare, autoimmune blistering disease of the skin & mucous membranes. Caused by circulating autoantibodies directed against desmoglein (cell surface adhesion molecule) in epidermis
Presence of antibodies at site of blister formation Type II hypersensitivity Results in destruction of cell-to-cell adhesion (separation of keratinocytes), called acantholysis, and blisters!!! Prevalent in people ages 40-50 (middle age) |
Pemphigus
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Pemphigus Types
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(1) vulgaris- most common form with oral lesions that precede blistering (2) vegetans- large blisters occur in tissue folds (3) foliaceus- milder form that rarely involves oral mucous membranes (4) erythematosus- less widely distributed lesions and associated with lupus
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Inflammation of the skin & mucous membranes
Caused by reactions to drugs or herpes “Bull’s eye” or “target” lesions on skin surface Type III hypersensitivity Lesions occur in groups over a period of 2-3 weeks; single or multiple vesicles or bullae may arise accompanied by pruritus & burning; lesions heal within 3-4 weeks Most common in ages 20-40 (early adulthood) |
Erythema multiforme
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Erythema multiforme types
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(1) Stevens-Johnson syndrome- severe bullous form (2) toxic epidermal necrolysis- numerous erythematosus bullous lesions occur on skin & mucous membranes and is probably related to drug reactions
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causes of cutaneous infections Bacterial:
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Bacterial: S. aureus (MRSA) and β-hemolytic streptococci are most common causative microorganisms
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bacterial infection of the hair follicle that is commonly caused by S. aureus. Lesions appear as pustules surrounded by erythema- most common on scalp. Prolonged skin moisture, skin trauma and poor hygiene associated.
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Folliculitis
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inflammation of the hair follicle that may develop after folliculitis and spread into surrounding dermis, caused by S. aureus. The initial lesion is a deep, red, firm nodule that is 1-5 cm in size.
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Furuncles (boils!!!):
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collection of infected hair follicles.
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Carbuncles
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infection of the dermis and subcutaneous tissue that is usually caused by Staphylcoccus
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Cellulitis
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acute superficial infection of the upper dermis most often caused by β-hemolytic streptococci. Fever, malaise and chills precede onset by 4 hours to 20 days.
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Erysipelas
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superficial lesion that is caused by coagulase-positive Staphylococcus or β-hemolytic
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Impetigo
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2 types of Impetigo:
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vesicular and bullous
|
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It is a latent infection in the basal ganglia
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Varicella-zoster virus
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dermatophytes, which thrive on keratin, cause fungal infections. Fungal disorders are known as
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mycoses
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Mycoses are called ____ when caused by dermatophytes
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tinea
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caused by the yeastlike fungus Candida albicans
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Candidiasis
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Partial-thickness that involves only the epidermis
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First-degree burn
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Superficial partial-thickness: thin-walled, water-filled blisters that develop within a few minutes of injury.
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Second-degree burn
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Full-thickness that involves destruction of the entire epidermis, Painless because nerve endings are destroyed
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Third-degree burn
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dermatophytes, which thrive on keratin, cause fungal infections. Fungal disorders are known as
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mycoses
|
|
Mycoses are called ____ when caused by dermatophytes
|
tinea
|
|
caused by the yeastlike fungus Candida albicans
|
Candidiasis
|
|
Partial-thickness that involves only the epidermis
|
First-degree burn
|
|
Superficial partial-thickness: thin-walled, water-filled blisters that develop within a few minutes of injury.
|
Second-degree burn
|
|
Full-thickness that involves destruction of the entire epidermis, Painless because nerve endings are destroyed
|
Third-degree burn
|