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osteochondroma
- MC BBT of the appendicular skeleton
- either pedunculated or sessile
- hereditary multiple exostosis (HME) are multiple osteochondromas
- 20% undergo malignancy
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Unicameral Bone Cyst aka Simple Bone Cyst
- benign
- diaphyseal/metaphyseal location
- centrally located
- less than 20 yo
- fluid filled
- associated with fallen fragment sign
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Aneurysmal Bone Cyst
- diaphyseal/ metaphaseal location, eccentrically loacted
- less than 20 yo
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Giant Cell Tumor
- epiphyseal/metaphyseal location
- 20-40 yo
- 20% of time quasi malignant
- assocated with soap bubble lesion
- benign
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Chondroblastoma
- epiphyseal/metaphyseal location
- less than 20 yo
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osteoid osteoma
- night pain relieved by aspirin
- radiolucent central nidus with severe reactive sclerosis and bone expasion
- benign
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Brodie's Abscess
night pain relieved by aspirin appears like an osteoid osteoma
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Enchondroma
- MC BBT of hand
- stippled appearance
- multiple enchondromas is ollier's disease
- ollier's - 10-50% rate of malignant degeneration
- Soft tissue calcification is known as maffucci's syndrome
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Hemangioma
- MC BBT of spine
- vertical striations
- corduroy cloth appearance
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Enostoma
- bone island
- round or oblong radiopaque lesion
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Osteopoikilosis
multiple bone island
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Osteoblastoma
MC BBT to affect the neural arch
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Osteoma
- MC BBT affects the skull
- found in frontal sinus most commonly and best seen on the calwell projection
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Fibrous Dysplasia
- monostotic form associated with rind sign
- polystotic form
- physiologic resorption of normal bone replaced by fibrous tissue
- causes deformity
- saber shin tibia and sheppards crook
- ground glass appearance
- cafe au lait spots
- coast of maine appearance
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Neurofibromatosis
- familial history
- pt may present with scoliosis
- cervical kyphosis
- vertebral body scalloping with IVF enlargement
- cafe au lait spots with Coast of California appearance
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Multiple Myeloma aka Plasma Cell Sarcoma
- >50 yo cachexia, weightloss, anemia, MC primary malignancy of bone, malignant proliferation of plasma cells infiltrating bone marrow
- multiple dark densities that are similar in size (punched out lesions) can cause pathological collapse
- rain drop skull
- labs: M spike on the immunoelectrophoresis 2. reversal of the albumin globulin ration 1:1, 3. bence jones proteinuria, 4. elevated ESR,
- test- bone scan cold
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Metastatic Disease
- lytic and blastic
- MC malignant tumor of bone
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Lytic Metastatic
- >40 yo recent unexplained weight loss, skeletal pain, worse at night
- trabeculae reabsorbed turns the bone darker in color
- moth eaten or permeative pattern of destruction
- eats away pedicle of bone
- swiss cheese appearance in the skull
- labs: alkaline phophatase
- special test: bone scan- hot
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Hodgkin's Disease
- MC metastasis in 20-40 yo males
- bone becomes more radiopaque in color: ivory white vertebrae with anterior body scalloping
- unilateral hilar lymphadenopathy in caucasians seen on the PA chest view
- need biopsy to confirm
- Reed Sternberg Cells
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Blastic Metastasis
- >40 yo ivory white vertebrae
- MC cause is from prostatic carcinoma
- Labs: increased alkalkine phosphatase
- special test bone scan-hot
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Paget's aka osteitis deformans
- males >50 yo
- stages: 1. lytic or destructive 2. combined 3. sclerotic 4. malignant
- causes cortical thickening bone expansion, picture frame vertebrae bowing deformities
- labs: increased alkaline phosphatase and urinary hydroxyproline
- tests: bone scan- hot
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Osteosarcoma
- MC malignancy found in children
- ages 10-30
- periosteal rxn that is spiculated, radiating, sunburst in appearance
- labs: increased alkaline phosphatase
- hot bone scan
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Chondrosarcoma and Fibrosarcoma
>40 yo creates a spiculated radiating sunburst periosteal rxn of bone
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Ewings Sarcoma
10-25 yo MC found in diaphysis of long bones. Permeative lesion that causes a multiparalleled onion skin type of periosteal rxn. Bone expansion, codman's triangle, saucerization
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Chordoma
- >40 yo aberrant notochordal cell tumor.
- MC found in Sacrum
- 2nd MC location is skull
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Scoliosis
- Females 13-19 names for the side of the major convexity
- Rotatory Scoliosis- sp deviated to concavity
- Simple Scoliosis- sp deviate to convexity
- Cobb's and risser ferguson's to measure
- measurments for 25 yo and younger:
- under 20- adjust and monitor
- 21-40 send to orthopedist for bracing
- over 40 is surgical
- over 50 is cardio pulmonary compromise
- monitor scoliosis1. risser's sign, wrist films, tanner stages
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Rheumatoid Arthritis or Still's Disease in children
- Bilateral uniform loss of joint space, rat bite erosions, pannus formation, localized periarticular osteoporosis, symmetrical distribution, atlanto-axial instability
- Bouchards PIP, Haygarth MCP DIP is spared Swan neck and boutonneire deformity, ulnar deviation, baker's cyst
- MC cause of bilateral protrusio acetabuli
- Labs: RA latex, FANA, ESR, CRP, normocytic normochromic anemia
- dry eyes and mouth presented is called Sjogrens
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Ankylosing Spondylitis AKA Marie Strumpell
- Males 15-35 yo starts in SI joints, LBP, morning stiffness, Forester's bowstring and Lewin's supine iritis
- Si joints bilateral fusion
- shiny corner sign, bilateral marginal syndesmophytes, squaring of body, bamboo spine, dagger sign, trolley track sign
- labs: HLAB27 adn ESR
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Enteropathic Arthropathy
- Identical to AS with GI Dysfxn
- chrons, diverticulitis, ibs
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Psoriatic Arthritis
- males 20-50 yo silver scales and pitted nails cocktail sausage digits
- increased joint space, pencil in cup deformity, mouse ear deformity, ray sign, atlantoaxial instability, non marginal syndesmophytes
- HLAB27 positive
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Reiter's
- males 20-30 plus or minus, cant see cant pee cant dance with me
- HLAB27 positive
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Systemic Lupus Erythematosus
- females, sunlight precipitates a skin rash (malar or butterfly rash) alopecia, raynaud's penomenon can cause ulnar deviation of the phalanges
- LE prep, FANA, RA latex ESR
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Scleroderma aka Progressive Systemic Sclerosis
- females 30-50 yo CREST syndrome erosions of the distal tufts
- labs: FANA, RA latex
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Osteitis COndensans Ilia
- multiparous females
- 20-40 yo bialteral symmetric triangular sclerotic areas on the lower half of the ilium
- joint space is normal
- self resolving
- no labs
- trochanteric belt
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DJD (OA0
- non inflammatory, MC in fingers and weight bearing joints, usually stiffens with rest adn improves with activity
- complications inclue spinal stenosis and ivf encraochment
- MC at C5/C6
- heberden's DIP and Bouchard's PIP
- asymmetrical non uniform loss of joint space
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DISH
- males >40 yo associated with diabetes mellitus
- candle was drippings, 4 contguous segments infolved ALL
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Neurogenic Arthropathy
- Secondary to impaired sensory fx in joints. seen wtih diabetes, tabes dorsalis, syphilis and syringomyelia
- 6D's: distention, density of subchondral sclerosis, debris, dislocation, disorganization, destruction of bone
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Synoviochonrometaplasia
- MC join affected in the knee
- Results in multiple loose bodies within the joint that are round or ovoid in shape
- popcorn like look in the knee
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Gout
- males >40 yo.
- overproductoin of uric acid
- foods high in purines
- MTP of the big toe (podagra)
- overhanging margin: juxta articular erosions
- Labs: increased uric acid, esr
- take: acute-colchicine, chronic allopurinol
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Calcium Pyrophosphate Dihydrate Crystal Deposition Disease (CPPD Pseudogout)
- thin linear calcification parallel to the articular cortex within the joint space.
- called chondrocalcinosis when affecting carilage
- MC in the knee
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Hydroxyapatite Deposition Disease HADD
- MC affects shoulder joint
- round or oval calcifications near the insertion of a bursa or tendon
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Septic Arthritis
- fever, chills, history of trauma, surgery and warm tender swollen joint
- WBC Count
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Preiser's
AVN of carpal scaphoid
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Osgood Schlatter's
AVN of tibial tuberosity
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