Bones, Joints and Soft Tissue Flashcards

1
Q

MC skeletal dysplasia and MAJOR cause of dwarfism

A

ACHONDROPLASIA

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2
Q

MC lethal form of dwarfism

A

THANATOTROPHIC DYSPLASIA

respiratory insufficiency - USUAL CAUSE OF DEATH

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3
Q

MC inherited disorder of CT

AD

extreme skeletal fragility d.t. TOO LITTLE BONE

A

OSTEOGENESIS IMPERFECTA

TYPE I COLLAGEN

TYPE OI - MOST LETHAL

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4
Q

Impaired osteoclast function –> EXCESSIVE BONE FORMATION

WOVEN deposited bone

A

OSTEOPETROSIS (MARBLE BONE DISEASE)

(-) medullary canal
ERLENMEYER FLASK DEFORMITY

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5
Q

MC skeletal malignancy

A

METASTASIS

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6
Q

MC primary malignant bone tumor

A

OSTEOSARCOMA

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7
Q

2nd MC malignant matrix producing tumor of the bone

A

CHONDROSARCOMA

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8
Q

2nd MC group of bone sarcomas in CHILDREN

A

EWING SARCOMA

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9
Q

MC BENIGN BONE TUMOR

adolescence early adulthood

SOLITARY

METAPHYSIS

KNEE

A

OSTEOCHODNROMA

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10
Q

Increased but disordered and structurally unsound bone

BONE PAIN

axial, skeleton, proximal femur

A

PAGET DISEASE (OSTEITIS DEFORMANS)

COMPLICATIONS:
high output failure - Pagetic bone as AV shunt
OSTEOSARCOMA AND FIBROSACROMA - MOST DREADED

mosaic pattern of lamellar bone
jigsaw puzzle like appearance d.t. cement lines

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11
Q

FRACTURE HEALING

A

0-2 weeks - PROCALLUS

2-3 weeks - BONY CALLUS (WOVEN)

3 weeks - months - LAMELLAR bone formation

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12
Q

< 2 cm

APPENDICULAR skeleton - femur or tibial

relieved by NSAIDs

MARKED reactive bone formation

A

OSTEOID OSTEOMA

radiofrequency ablation

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13
Q

> 2 cm

AXIAL skeleton - posterior spine

NOT relieved by NSAIDs

A

OSTEOBLASTOMA

en bloc excision

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14
Q

METAPHYSIS

CODMAN triangle - periosteal lifting
SUNBURST appearance - infiltrative borders

A

OSTEOSARCOMA

lace like pattern
broad sheets, primitive trabeculae

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15
Q

Benign tumor of HYALINE cartilage

20-50

METAPHYSIS

A

CHONDROMA

Ollier
Maffuci

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16
Q

2nd MC group of bone disorders in CHILDREN

<20 y/o

DIAHYSIS (femur)

(+) systemic symptoms

A

EWING SARCOMA

lytic lesion
ONION SKIN - periosteal reaction

MICROSCOPIC:
uniform, small, round blue cells
scant, clear cytoplasm
HOMER WRIGHT ROSETTES

17
Q

BENIGN but LOCALLY AGGRESSIVE

INCREASED RANKL levels –> increased bone resorption

3rd-5th decade

EPIPHYSIS

A

GIANT CELL TUMOR (OSTEOCLASTOMA)

18
Q

Benign tumor that shows features of localized developmental arrest of bone

CHINESE CHARACTER - curvilinear trabeculae of woven bone

NO OSTEOBLASTIC RIMMING

A

FIBROUS DYSPLASIA

ASSOCIATED DISEASES:
Mazabraud syndrome - polyostotic FD + soft tissue myxomas

McCune-Albright Syndrome - polyostotic FD + Cafe au lait spots + precocious puberty

19
Q

Mechanical injury to articular cartilage

WEIGHT BEARING JOINTS - knees, hips

cartilage degeneration and fragmentation
BONE EBURNATION
OSTEOPHYTES
subchondral cysts
minimal inflammation

A

OSTEOARTHRITIS

BOUCHARD nodes - PIP
HEBERDEN - DIP

20
Q

Autoimmunity

cartilage destruction caused by CD4 T cells and antibodies

SMALL JOINTS OF FINGERS –> MULTIPLE JOINTS

PANNUS
severe chronic inflammation
ANKYLOSIS
rheumatoid nodules

EXTRA-ARTICULAR INVOLVEMENT

(+) systemic symptoms

A

RHEUMATOID ARTHRITIS

RHEUMATOID FACTOR

ANTI-CITRULLINATED PEPTIDE ANTIBODY

SWAN NECK
BOUTONNIERE

21
Q

usually MONOARTICULAR

1st MTP of the BIG TOE - MC joint involved

MORE INTENSE inflammation

A

GOUT

monosodium urate
NEEDLE shaped
NEGATIVELY birefringent (YELLOW)

22
Q

mono or polyarticular

KNEE - MC

A

PSEUDOGOUT

calcium pyrophosphate dihydrate
RHOMBOID
POSITIVELY birefringent (BLUE)

23
Q

Pathognomonic hallmark of gout

A

TOPHI

24
Q

MC subtype of rhabdomyosarcoma

A

EMBRYONAL

mixture of primitive round and spindle cells

SARCOMA BOTYOIDES - BEST PROGNOSIS