MSB pathology Flashcards

(50 cards)

1
Q

How to treat trochanteric bursitis? (Inlammation of gluteal tendon and bursa lateral to greater trochanter)

A

NSAIDs, heat, stretching

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2
Q

Housemaids knee AKA..

A

prepateller bursitis

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3
Q

Causes of housemaids knee?

A

repeated trauma/pressure from excessive kneeling

Can be from gout/infection as well

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4
Q

What is a bakers cyst?

A

popliteal fluid collection that commonly communicates with synovial space

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5
Q

What pathologies is bakers cyst related to?

A

Rheumatoid and osteoarthritis

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6
Q

How does a rupture of a bakers cyst present?

A

similar to DVT

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7
Q

What is De Quervain tenosynovitis?

A

Thickening of abductor pollicis longus and extensor policies brevis. Pain or tenderness at radial styloid

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8
Q

What is a positive Finkelstein test

A

pain at radial styloid with active or passive stretch of thumb tendons

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9
Q

Presentation of gangliion cyst

A

fluid-filled swelling overlying joint or tendon sheeth, most commonly on dorsal side of wrists

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10
Q

Presentation of illiotibial band syndrome

A

pain at lateral femoral epicondyle from overuse of lateral knee (common in runners)

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11
Q

Limb compartment syndrome defining criteria

A

Difference than 30 mmhg or less between the tissue compartment and diastolic bp

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12
Q

Medial tibial stress syndrome presentation

A

Shin pain in runners and military recruits

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13
Q

Medial tibial stress syndrome aka

A

shin splints

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14
Q

Plantar fascitis

A

Inflammation of plantar aponeurosis characterized by heel pain - worse with first steps in the morning

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15
Q

What is developmental dysplasia of the hip?

A

Abnormal acetabulum development in newborns that results in hip instability/dislocation

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16
Q

What is the confirmatory test for developmental dysplasia of the hip?

A

ULTRASOUND (not xray bc cartilage isn’t ossified)

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17
Q

What is Legg-Calve-Perthes disease?

A

Idiopathic avascular necrosis of the femoral head

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18
Q

who gets Legg-Calve-Perthes disease?

A

Children aged 5-7,more commonly males

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19
Q

What will the initial XRAY of Legg-Calve-Perthes disease look like?

A

Normal, initially

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20
Q

What is Osgood-Schlatter disease (traction apophysitis)?

A

Overuse injury caused by repetitive strain and chronic avulsion of secondary ossification center of proximal tibial tubercle

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21
Q

Who gets Osgood-Schlatter disease ?

A

teengers after their growth spurt. Common in runners and jumping atheletes

22
Q

What is patellofemoral syndrome and who gets it?

A

overuse injury that commonly presents in young, female athletes as anterior knee pain
-gets worse with prolonged sitting or weight-bearing on flexed knee

23
Q

How to treat patellofemoral syndrome?

A

NSAIDs and thigh muscle strengthening

24
Q

Slipped capital femoral epiphysis presentation?

A

Seen in obese preteens early adolescent children with hip/knee pain and altered gait

25
Slipped capital femoral epiphysis treatment
surgery
26
What is a greenstick fracture?
incomplete fracture following bending stress
27
What is a torus fracture?
when the cortex buckles on one side due to compression
28
Pathophys of achondroplasia
Constitutive activation of fibroblast growth factor receptor inhibits chondrocyte proliferation -often from autosomal dominant mutation
29
Osteoporosis pathophys
trabecular and cortical bone los mass and interconnections - due to increased bone resorption related to decreased estrogen and old age - may be secondary to drugs
30
Which drugs may promote osteoporosis?
Steroids, alcohol, anticonvulsants, anticoagulatnts, etc.
31
Why do many anticonvulsants promote bone loss?
They upregulate CYP450 which increases vit D breakdown
32
Diagnosis of osteoporosis
DEXA scan with T-score <2.5 or by fragility fracture (hip or vertebra fracture from fall at normal height)
33
Treatment of osteoporosis
bisphosphonates, teriparatide, SERMs, rarely calcitonin, denosumab
34
Osteopetrosis pathophys
Defective osteoclasts lead to failure of normal bone resorption ->thickened, dense bones that are prone to fracture Caused by mutations in carbonic anyhydrase II
35
What mutation occurs in osteopetrosis?
Carbonic anyhdrase II
36
Osteopetrosis complications
overgrowth of cortical bone fils. marrowspace --> pancytopenia, intramedullary hematopoiesis, may result in cranial nerve impingement and palsies
37
Treatment for osteopetrosis
Bone marrow transplant - may be curative as osteoclasts derive from monocytes
38
Infantile form of osteopetrosis inheritance
autosomal recessive
39
Albers-Schonberg disease
autosomal dominant form of osteopetrosis
40
Pathophys of osteomalacia/rickets
Defective mineralization of osteoid or cartilaginous growth plates
41
Xray findings in osteomalacia
Looser zones (pseudofractures)
42
Xray findings in rickets
epiphyseal widening and metaphyseal cupping/fraying
43
clinical findings in children with rickets
Bow legs (genu varum), bead-like costochondral junctions(rachitic rosary), craniotabes (soft skull)
44
Labratory findings in osteomalacia/rickets
``` Low vitamin D Low serum Ca Increased PTH Decreased serum phosphate Increased ALP from osteoblasts ```
45
Osteitis deformans aka
Pagets disease
46
Pagets disease pathophys
Increased osteoclast and osteoblastic activity causes increased bone remodelling. Forms poor quality bone.
47
Lab values in pagets disease
everything normal except increased ALP
48
Complictions of pagets disease
Chalk stick fractures High output heart failure (arteriovenous shunts) Osteosarcoma Hearing loss
49
Four stages of pagets disease
Lytic - osteoclasts Mixed - osteoclasts + osteoblasts Sclerotic - osteoblasts Quiescent - minimal osteoclast/osteoblast activity
50
Treatment of pagets
bisphosphonates