Musculoskeletal Disorders Flashcards

Differentiate among musculoskeletal disorders such as soft tissue injuries, joint injuries, fractures, and infections. Explain the process of bone healing and the pathophysiology of impaired bone healing. Compare and contrast the etiology, pathophysiology, and manifestations of metabolic bone disorders such as osteoporosis, osteomalacia, Paget Disease, rheumatoid arthritis, osteoarthritis, systemic lupus erythematosus, ankylosing spondylitis, and gout. Describe skeletal disorders in children suc

1
Q

what is the most common cause of musculoskeletal injuries:
childhood:
adults under 45:
adults over 65:

A

falls (bikes) sports
MVA
falls

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2
Q

what are the 3 examples of soft tissue injury?

A

contusion
hematoma
laceration

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3
Q

what are the 3 kinds of joint injuries?

A

strain
sprain
dislocation

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4
Q

what is a strain?

A

An injury to a muscle or tendon

due to overstretching or tearing,

from overuse or sudden contraction.

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5
Q

What is a sprain?

A

An injury to a ligament c

Caused by twisting or pulling forces,

excessive joint movement

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6
Q

How do strains and sprains differ?

A

Strains affect muscles or tendons.

Sprains affect ligaments.

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7
Q

What are the grades of a sprain?
1
2
3
4

A

Grade 1: Mild stretch, microscopic tears, minimal swelling

Grade 2: Partial tear, moderate swelling/bruising

Grade 3: Complete tear, severe swelling/instability

Grade 4: Complete tear with dislocation or ligament avulsion

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8
Q

What are the pathophysiology and symptoms of a strain?

A

Patho: Overstretching or tearing of muscle/tendon fibers = inflammatory response = swelling = repaired with collagen

Symptoms: Pain, swelling, cramping, weakness, limited ROM

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9
Q

What are the pathophysiology and symptoms of a sprain?

A

Patho: Ligaments stretched or torn due to trauma = inflammatory response = swelling = repaired with collagen

Symptoms: Joint instability, pain/tenderness, swelling, bruising, ↓ function

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10
Q

What is a dislocation?

A

When the ends of bones are forced out of their normal positions in a joint, leading to loss of function, pain, and visible deformity

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11
Q

What are common signs of a dislocation?

A

Visible deformity

Severe pain

Inability to move the joint

Swelling

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12
Q

What often causes dislocations?

A

Trauma
falls
sports injuries that apply force to a joint beyond its normal range of motion.

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13
Q

What is a contusion?

A

A soft tissue injury caused by blunt force trauma that leads to bruising due to ruptured blood vessels, without breaking the skin

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14
Q

What are the symptoms of a contusion?

A

Pain
swelling
discoloration at the site of injury

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15
Q

patho of contusion

A

trauma = BVs rutpure = bleed into tissue = inflammatory repsonse = swelling = RBC’s breakdown (coloration) = body reabosorbs blood and repairs tissue

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16
Q

What is a hematoma?

A

A localized collection of blood outside blood vessels, often within tissue, forming a swollen, firm lump.

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17
Q

How is a hematoma different from a contusion?

A

A hematoma is usually larger, causes more pressure, and can occur deeper in tissues; a contusion is a more superficial bruise.

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18
Q

What are common symptoms of a hematoma?

A

Swelling
tenderness
discoloration
palpable mass under the skin
heat
restricted ROM

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19
Q

What is a laceration?

A

A deep cut or tear in the skin or flesh, potentially damaging underlying tissues like muscles, tendons, or nerves.

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20
Q

What are typical signs of a laceration?

A

Bleeding, pain, exposed tissue, and an open wound with irregular or jagged edges.

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21
Q

What is the major concern with lacerations?

A

Infection risk, blood loss, and potential damage to deeper structures like nerves and tendons

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22
Q

causes of lacerations (4)

A

trauma, sharp objects, surgery, bites

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23
Q

What are common manifestations of a fracture? (6)

A

Pain and tenderness

Swelling and bruising

Deformity

Loss of function

Crepitus (grating sound)

Bleeding or exposed bone (in open fractures)

(dislocation, fat embolism and infections are complications)

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24
Q

What is a transverse fracture?

A

A break that is straight across the bone, usually caused by a bending force.

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25
What is an oblique fracture?
A break that occurs at an angle across the bone.
26
What is a comminuted fracture?
The bone is shattered into three or more pieces.
27
What is a segmental fracture?
The bone is broken in two places, creating a segment between the breaks.
28
What is a greenstick fracture (commonly in children)?
A partial break in the bone where one side bends and the other side breaks kids bones are stronger / more resilient
29
What is a compression fracture?
Bone is crushed (common in vertebrae).
30
patho of healing: (
necrosis of damaged cells = inflammatory response = fibroblasts produce collagen (and CT) at site = formation of collagen bundles = increase in tensile strength
31
what are ligaments?
bands of fibrous CT that connect bones to other bones
32
what are tendons?
cords of fibrous CT, formed from the sheath surrounding tisses connect muscles to bones
33
What is an open (compound) fracture?
The bone breaks through the skin, increasing infection risk.
34
What is a closed (simple) fracture?
The bone breaks but does not pierce the skin.
35
how are fractures classified?
location (proximal, midshaft, distal) direction (transvere, linear, oblique, spiral) type (displaced, communities, greenstick)
36
what are the 3 causes of fractures?
sudden (MVA, fall, trauma) stress (overuse or overwork) pathologic (osteoporosis)
37
what is a complete fracture?
bone is broken all the way through
38
what is an incomplete fracture?
bone is damaged but in one piece
39
What is the first phase of fracture healing?
(first 1 - 2 days) Hematoma Formation – Bleeding at the fracture site forms a blood clot (fibrin wall seals of fx site) and starts inflammation.
40
What is the second phase of fracture healing?
Inflammation/Fibrocartilaginous Callus Formation – new capillaries at the fx site are organized and form a procallus then ... Fibroblasts and chondroblasts create collagen and cartilage to bridge the bone connected but weak and lack stability
41
What is the third phase of fracture healing?
(3 - 4 weeks after) Reparative phase/Bony Callus Formation – Osteoblasts form spongy bone, converting the soft callus into hard bone. heals from outside in
42
What is the fourth phase of fracture healing?
Bone Remodeling – Woven(spongy) bone is removed by osteoclasts and are replaced with strong lamellar (compact) bone, restoring original shape and strength
43
What is delayed union?
A fracture that takes longer than expected to heal due to poor blood supply, infection, or instability.
44
What is malunion?
The bone heals in an abnormal position, usually from improper alignment during healing
45
What is non-union?
The bone ends fail to unite completely, often due to trauma, infection, or poor nutrition
46
What are the symptoms of a fat embolism? (7)
CP SOB low grade fever Respiratory distress Petechial rash Confusion or seizures Tachycardia
47
What is a fat embolism?
fat globules (from bone marrow) enter the bloodstream, possibly lodging in lungs or brain after LONG bone fracture
48
What is Compartment Syndrome?
A serious condition where increased pressure within a muscle compartment compromises circulation and nerve function, potentially leading to tissue death.
49
What causes Compartment Syndrome? (5)
Fractures (especially long bones) Crush injuries Tight casts or bandages Severe burns Prolonged limb compression (e.g., during surgery)
50
What are the late signs of Compartment Syndrome? (The 6 Ps)
Pain Pallor Pulselessness Paresthesia (tingling/numbness) Paralysis Poikilothermia (cool limb)
51
What are the early signs of Compartment Syndrome?
Severe, unrelenting pain (out of proportion to injury) Pain on passive stretch of the muscle Tense, swollen compartment
52
What is the pathophysiology of Compartment Syndrome?
Pressure builds up inside a closed muscle compartment d/t fascia Blood flow is reduced, leading to ischemia Nerves and muscles begin to die if pressure isn’t relieved quickly
53
What is Osteomyelitis?
A bone infection, most often caused by bacteria (commonly Staphylococcus aureus), leading to inflammation, bone destruction, and necrosis
54
What is the most common organism that causes Osteomyelitis?
Staphylococcus aureus
55
What is the pathophysiology of Osteomyelitis? (4)
Bacteria enter bone and proliferate → trigger inflammatory response Pus forms and increases pressure within bone Leads to vascular compromise and necrosis Formation of sequestrum (dead bone) and involucrum (new bone around infected area)
56
What are the common causes (etiology) of Osteomyelitis?
Open fractures or trauma Surgical contamination (e.g., orthopedic implants) Hematogenous spread (bacteria from bloodstream infects bone) Diabetic foot ulcers or chronic wounds
57
What is an involucrum?
New bone formation that surrounds the area of infection/sequestrum.
58
What is a sequestrum?
A piece of dead bone that has become separated from healthy bone due to infection
59
What are the manifestations of Osteomyelitis? (5)
Fever and chills Localized bone pain Swelling, redness, and warmth over site Drainage (in chronic cases) Limited range of motion near affected area
60
how do benign and malignant bone tumors differ from one another?
benign have smooth edges Malignant are poorly defined and lack borders
61
What is a neoplasm?
An abnormal growth of tissue, which may be benign or malignant. In bone, neoplasms can originate in the bone (primary) or spread from another site (metastatic)
62
When are bone neoplasms most likely to occur?
During adolescence (due to rapid bone growth) In older adults (especially metastatic bone disease)
63
What is an osteosarcoma?
A malignant bone tumor common in adolescents, often affecting the long bones (femur, tibia). It's aggressive and may metastasize to the lungs.
64
what is the most common and what is the most lethal bone neoplasm?
common: osteosarcoma (75% under 20 yr) lethal (in kids and YAs): ewing sarcoma
65
who is most commonly affected by osteosarcoma?
Teenagers and young adults, especially during growth spurts
66
What are symptoms of osteosarcoma? (5)
deep, localized, persistent localized bone pain nighttime awakening (worse pain) Swelling or mass over the bone Decreased function or range of motion Possible fracture
67
What is Ewing Sarcoma?
A highly malignant tumor found in children and young adults, often affecting the pelvis, femur, or long bones. Associated with a chromosomal translocation.
68
What are symptoms of Ewing Sarcoma?
Bone pain Fever and fatigue Swelling and warmth at tumor site Leukocytosis and elevated ESR May mimic infection
69
What are the key differences between Ewing Sarcoma and Osteosarcoma?
Ewing Sarcoma: * More common in children and young teens * Affects pelvis and central long bones * Presents with pain + systemic symptoms (fever, fatigue) * Responsive to radiation and chemo * Associated with chromosomal translocation (t11;22) Osteosarcoma: * More common in teens and young adults * Affects ends of long bones (e.g., femur, tibia) * Presents with localized bone pain and swelling * Treated with surgery and chemo (less sensitive to radiation) * Often linked to bone growth spurts or genetic factors
70
What is osteoporosis?
A metabolic bone disease characterized by decreased bone mass and density (loss of mineralized bone), leading to fragile bones and increased fracture risk
71
What causes (risk factors) osteoporosis? (9)
Aging gender (women) hyperparathyroidism Postmenopausal estrogen loss diet: Low calcium and vitamin D intake, low salt Sedentary lifestyle Long-term corticosteroid use Alcohol, smoking, steroids, excess caffeine Genetic predisposition
72
What is the pathophysiology of osteoporosis?
Bone resorption (breakdown) exceeds bone formation, resulting in porous, weak, thin bones with decreased structural integrity.
73
What are the common manifestations of osteoporosis? (5)
Fragility fractures (especially spine, hip, wrist) Loss of height Kyphosis (hunched back) Back pain and deformity Decreased mobility in severe cases
74
what is the adult form of rickets?
osteomalacia
75
What is osteomalacia?
A bone disorder in adults where bones become soft due to defective mineralization, typically from vitamin D and Ca deficiency.
76
What causes osteomalacia? (5)
Vitamin D deficiency Malabsorption of Ca, PO, and vit D (e.g., celiac disease) Chronic kidney or liver disease Certain medications (e.g., anticonvulsants) Lack of sunlight exposure
77
What is the pathophysiology of osteomalacia?
Inadequate vitamin D → ↓ calcium and phosphate absorption Impaired bone mineralization → bones are soft, weak, and more prone to deformity
78
What are the manifestations of osteomalacia?
Bone pain and tenderness (especially hips, lower back) Muscle weakness Fractures with minimal trauma Difficulty walking or waddling gait Fatigue and generalized discomfort
79
What is Paget Disease?
A chronic bone disorder characterized by excessive bone turnover, resulting in abnormal bone formation and weak, deformed bones.
80
What causes Paget Disease?
The exact cause is unknown, but it is thought to involve a combination of genetic factors (e.g., mutations in SQSTM1 gene) and possibly viral infections that affect bone metabolism
81
What is the pathophysiology of Paget Disease?
Excessive osteoclastic activity leads to increased bone resorption Abnormal/disorganized osteoblast activity creates disorganized new bone The bone becomes thickened and weakened, leading to deformities and fragility.
82
Which bones are most commonly affected by Paget Disease? (4)
Pelvis Spine Skull Long bones (femur, tibia)
83
What are common manifestations of Paget Disease?
Bone pain (often in spine, pelvis, or long bones) Deformities (e.g., bowed legs, enlarged skull) (expansion and distortion) Fractures due to weakened bone Hearing loss (due to involvement of the skull and ear bones) Headaches and dizziness Arthritis (secondary to abnormal joint stresses) Cardiovascular disease: aortic stenosis
84
What complications can arise from Paget Disease?
Osteoarthritis from abnormal joint stresses Fractures due to weakened bone Hearing loss (from skull involvement) High-output heart failure (rare, due to increased blood flow in affected bones) high risk for osteogenic sarcomas
85
what is the purpose of the synovial membrane?
lubricates joints maintain joint stability
86
what is the purpose of articular cartilage? (4)
smooth weight bearing low friction (w synovial fluid) decreases mechanical stress on bone
87
What is Rheumatoid Arthritis (RA)?
An autoimmune disease where the body’s immune system attacks the synovium (lining of the joints), leading to inflammation, pain, and eventual joint destruction.
88
What causes Rheumatoid Arthritis?
Genetic predisposition (HLA-DR4 gene) Environmental triggers (e.g., infections, smoking) Autoimmune response where the body mistakenly attacks its own joints
89
What is the pathophysiology of Rheumatoid Arthritis?
Immune system attacks the synovium, causing inflammation = immune complex formation = thick synovial membrane = accumulation of inflammatory cells The inflammation releases enzymes that damage cartilage and bone. Over time, this leads to joint deformities, loss of function, and potential systemic involvement (e.g., lungs, eyes).
90
What are the common manifestations of Rheumatoid Arthritis?
Morning stiffness (lasting >30 minutes) Joint swelling, pain, and warmth Symmetrical joint involvement (e.g., wrists, knees, hands) Fatigue (aches and pains) Rheumatoid nodules (firm lumps under the skin) Systemic symptoms like fever, weight loss, anorexia, anemia
91
What causes Osteoarthritis? (6)
Aging Wear and tear on joints Obesity (increased joint stress) Joint injuries or previous trauma Genetics Gender (more common in women)
92
What is the pathophysiology of Osteoarthritis?
Cartilage degenerates due to wear and tear, leading to bone-on-bone contact. Synovial inflammation (thickening) formation of osteophytes (bone spurs). Joint space narrowing and loss of motion.
93
What are the manifestations of Osteoarthritis? (6)
Joint pain, especially with movement or use Morning stiffness (usually resolves after 30 minutes) Crepitus (grating sound when moving the joint) Joint swelling (especially in the knee, hip, or hands) Decreased range of motion Heberden's and Bouchard's nodes (bony nodules in the fingers)
94
What is Ankylosing Spondylitis (AS)?
A chronic inflammatory disease that primarily affects the spine and sacroiliac joints, leading to fusion of the spine over time.
95
What is the cause of Ankylosing Spondylitis?
The exact cause is unknown, but it is strongly linked to the genetic marker HLA-B27, suggesting an autoimmune component.
96
What is the pathophysiology of Ankylosing Spondylitis? (3)
immune response to antigen Inflammation of the spine and sacroiliac joints causes pain and stiffness. Over time, inflammation leads to fibrosis and ossification (bone formation), resulting in the fusion of joints, which severely limits movement.
97
What are the manifestations of Ankylosing Spondylitis?
Low back pain and stiffness (worsens in the morning) Reduced spinal flexibility and spinal fusion Pain and swelling in the hips, shoulders, and other joints stooped posture Fatigue and systemic symptoms Uveitis (inflammation of the eye) may also occur
98
What is Gout?
A type of arthritis caused by the accumulation of uric acid crystals in the joints and kidney, leading to inflammation, redness, and pain.
99
What causes Gout?
Hyperuricemia (high levels of uric acid) in the blood Diet (foods high in purines, like red meat and shellfish) Genetics (family history) Renal issues (impaired uric acid excretion
100
What is the pathophysiology of Gout?
Uric acid builds up in the blood, forming crystals that deposit in joints (especially the big toe). The body reacts to the crystals with inflammation, leading to intense pain and swelling.
101
What are the manifestations of Gout?
Sudden, severe joint pain (often in the big toe, but can affect other joints like knees, elbows, and wrists) Redness and swelling of the affected joint Warmth around the joint Tophi (lumps of uric acid crystals under the skin, often in chronic cases)
102
why is gout common in the big toe?
gravity
103
What is Osteogenesis Imperfecta (OI)?
A genetic disorder commonly known as "brittle bone disease", characterized by fragile bones that fracture easily, often with minimal trauma.
104
What is the cause of Osteogenesis Imperfecta?
Mutations in the COL1A1 or COL1A2 genes, which impair the production of type I collagen, a key component of bone, skin, and connective tissues.
105
What is the pathophysiology of Osteogenesis Imperfecta?
The impaired collagen synthesis leads to brittle bones that fracture easily. Type I collagen abnormalities affect not just bones but also connective tissues, leading to other features like blue sclera and dentinogenesis imperfecta.
106
What are the manifestations of Osteogenesis Imperfecta? (6)
Frequent fractures (with minimal trauma) Blue sclera (bluish tint to the whites of the eyes) Hearing loss Dental problems (dentinogenesis imperfecta) Short stature Bone deformities (curved bones or bowing)
107
What are the classifications of Osteogenesis Imperfecta (OI)? Type I: (4)
Mildest form with fractures occurring after minor trauma. Normal life expectancy. Blue sclera (tint in the whites of the eyes). Hearing loss in early adulthood.
108
What are the classifications of Osteogenesis Imperfecta (OI)? Type II:
Most severe form, usually fatal in utero or shortly after birth. Multiple fractures present at birth, often leading to bone deformities and respiratory problems.
109
What are the classifications of Osteogenesis Imperfecta (OI)? Type III:
Severe form with frequent fractures and bone deformities. Short stature and blue sclera at birth, but sclera may change to a more normal color with age. Progressive deformities leading to severe disability
110
What are the classifications of Osteogenesis Imperfecta (OI)? Type IV:
Moderate severity; fractures occur later in childhood. Normal sclera (whites of the eyes are normal). Short stature, but better mobility than Types II and III.
111
What is Legg-Calve-Perthes Disease?
A childhood condition characterized by avascular necrosis of the femoral head, where interrupted blood supply leads to bone death and potential deformity.
112
What is the cause of Legg-Calve-Perthes Disease?
The exact cause is unknown, but it may involve trauma, coagulation disorders, or genetic predisposition, leading to a disruption in blood flow to the femoral head
113
What is the pathophysiology of Legg-Calve-Perthes Disease?
The interruption of blood flow to the femoral head causes bone necrosis leading to bone resorption Over time, this process may result in deformity of the femoral head if not properly managed.
114
What are the manifestations of Legg-Calve-Perthes Disease? (4)
Limping (often painless at first) Hip, thigh, or knee pain Limited range of motion in the hip joint Muscle wasting in the upper thigh due to disuse
115
Which age group is most commonly affected by Legg-Calve-Perthes Disease?
It primarily affects boys aged 4–8 years
116
What causes Osgood-Schlatter Disease?
Repetitive stress from activities like running and jumping, common in active adolescents during their growth spurts.
117
What is the pathophysiology of Osgood-Schlatter Disease?
The stress on the patellar tendon pulls on the tibial tubercle causing inflammation and microfractures at the growth plate of the tibia.
118
What are the manifestations of Osgood-Schlatter Disease? (4)
Pain and swelling below the kneecap Pain worsens with activity (especially running and jumping) Tenderness over the tibial tuberosity A visible bump may form at the tibial tubercle
119
What is the typical age group affected by Osgood-Schlatter Disease?
It commonly affects active adolescents, especially boys aged 10–15 during growth spurts
120
What is scoliosis?
A lateral curvature of the spine, often with rotational deformity, leading to an abnormal spine shape
121
What are the etiologies of scoliosis? (3)
Idiopathic (unknown cause, most common) Congenital (due to abnormal vertebral development) Neuromuscular (associated with conditions like cerebral palsy or muscular dystrophy)
122
What is the pathophysiology of scoliosis?
Uneven growth of the spine or muscle imbalances lead to an abnormal spinal curvature. In idiopathic cases, genetics may play a role.
123
What are the manifestations of scoliosis? (5)
Uneven shoulders or hips One shoulder blade more prominent than the other Asymmetrical waist or rib hump Back pain (in severe cases) Respiratory issues (if the curve is extreme)