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109 Cards in this Set
- Front
- Back
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Bubbly or lytic bone lesion
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FEGNOMASHIC
Fibrous dysplasia EG, Enchondroma GCT NOF Osteoblastoma Mets, Myeloma ABC SBC Hyperparathyroidism Infection Chondroblastoma |
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Multiple lytic bone lesions
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FEEMHI
Fibrous dysplasia Enchondromas EG Mets, myeloma Hyperparathyroidism Infection |
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Rib lesions
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FAME
Fibrous dysplasia ABC Mets, myeloma Enchondroma, EG |
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Lytic epiphyseal lesion
(also apophyseal, carpal and tarsal bones, patella) |
COGEM
Chondroblastoma (if <40 yo) Osteomyelitis GCT, geode EG Mets/myeloma (if >40yo) |
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Lytic lesion in posterior elements of spine
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OAT
Osteoblastoma ABC TB |
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Lytic bone lesion in a patient over 30 -
which lesions to LEAVE OUT of the ddx? |
CANES
Chondroblastoma ABC NOF EG SBC |
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Bony sequestrum in a lytic lesion
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FILE
Fibrosarcoma Infection Lymphoma EG osteoid osteoma (mimic) |
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Causes of geodes
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CARD and T
CPPD AVN RA DJD Trauma |
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Sclerotic bone lesion
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If over 40, METS (P,B,HL)
20-40 yo: chondroblastoma ABC NOF EG SBC fibrous dysplasia infection HPT (healing brown tumor) osteoid osteoma giant bone island |
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Bone lesion with endosteal scalloping
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Fibrous dysplasia
enchondroma cartilaginous tumor |
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Aggressive lytic bone lesion under age 10
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Ewing's
Osteosarcoma Lymphoma Osteomyelitis EG |
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Aggressive lytic bone lesion
age 10-20 |
Osteosarcoma
Ewing's sarcoma Lymphoma Osteomyelitis |
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Aggressive lytic bone lesion
age 20-30 |
Osteosarcoma
Lymphoma Ewing's MFH Osteomyelitis |
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Aggressive lytic bone lesion
age 30+ |
Myeloma/mets
Lymphoma Chondrosarcoma Fibrosarcoma/MFH Osteosarcoma Osteomyelitis |
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Permeative bone lesion in child:
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Ewing’s and other round cell CA
infection EG |
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Permeative lesion in older pt
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infection
mets, myeloma MFH reticulum cell sarcoma |
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Soft tissue tumors
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MFH
liposarcoma synovial sarcoma synovial osteochondromatosis PVNS hemangiomas |
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Malignant transformation of bony lesions:
fibrous dysplasia |
fibrosarcoma, OSA, MFH
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Malignant transformation of bony lesions: Paget’s
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OSA
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Malignant transformation of bony lesions:
osteomyelitis with draining sinus |
SCC
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Malignant transformation of bony lesions: radiation tx
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OSA, chondrosarcoma, MFH
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Malignant transformation of bony lesions: bone infarct
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fibrosarcoma, MFH
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Malignant transformation of bony lesions: Ollier’s
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chondrosarcoma
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Malignant transformation of bony lesions: Maffucci’s
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chondrosarcoma
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Malignant transformation of bony lesions: osteochondroma
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chondrosarcoma
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Cortical holes
(pseudopermeative lesion) |
- osteoporosis
(metacarpal cortex < 1/4-1/3 of metacarpal) - radiation - hemangiomas |
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Focal cortical thickening
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stress fracture
infection osteoid osteoma |
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Mets to bone (typical blastic and lytic)
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PBKTL
P – mostly blastic B – mixed K – purely lytic TL – mostly lytic |
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Hallmarks of DJD
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joint space narrowing (asymmetr)
subchondral sclerosis osteophytes subchondral cysts lack of osteoporosis or erosions |
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Joints that exhibit erosions with OA
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TMJ
SI AC pubic symphysis |
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Hallmarks of RA
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-hands – proximal. Ulnar dev.
-bilaterally symmetric -marginal erosions (incl uln styloid & triquetr) -periart & diff osteoporosis, subchondral cysts -ST swelling -jt space narrowing (JSN) -carpal instability, rotator cuff tear -distal clavicle resorption -protrusio acetabuli, A-a subluxation -2˚ DJD – severe JSN >> sclerosis & osteophytes |
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Hallmarks of fibrous dysplasia
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- NO periosteal rxn
- mention adamantinoma if in tibia or jaw - Typical: pelvis, prox femur, ribs, skull - "long lesion in long bone" - expansile medullary lytic lz w/ground glass; well-def sclerotic margin - bowing deformities; base of skull sclerotic - hot on bone scan - cherubism-mandible & maxilla - craniofacial -facial & frontal bones - pseudoarthrosis of tibia - Mccune Albright -polyostotic FD with café-au-lait spots &precocious puberty) |
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Hallmarks of enchondroma
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- must have Ca++ expt in phalanges
- no periostitis - tubular bones - chondroid calcifications - endosteal scalloping - pain is malignant - Ollier’s enchondromatosis, Mafucci’s enchondromatosis with multiple ST hemangiomas) |
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Hallmarks of EG
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- age<30
- lytic lesion can look aggressive - skull lesion beveled-edge appearance - sequestrum - floating tooth - vertebra plana - lung dz, pituitary, RES |
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Giant cell tumor characteristics
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- epiphyses closed
- epiphyseal & abuts articular surf in long bones - eccentric - well-def NONsclerotic border except flat bones - long tubular bone> spine/sacrum, 50% @knee |
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Lytic lesion, considering NOF, features to think of
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- age<30
- no periostitis - cortically based - metaphysis - also mention chondromyxoid fibroma |
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Characteristics of ABC
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- age<30, painful
- expansile, eccentric - fluid-fluid levels on MR - post elem spine, metaph long bones, pelvis - also mention osteoblastoma |
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Characteristics of SBC
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- age<30
- central, no periostitis - prox humerus, prox femur, calcaneus - fallen fragment sign |
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features of multiple myeloma
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- age>40
- plasmacytoma in ilium & sacrum, - cold on bone scan; do skel survey - vert bodies destroyed before pedicles - axial skeleton, long bones, punched-out lytic lesions, generalized osteopenia |
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features of osteosarcoma
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- ill-defined intramedullary metaphyseal mass
- extends through cortex - osteoid or chondroid matrix - aggressive periost rxn (Codman or sunburst) - telangiectatic form - purely lytic, mimics ABC - parosteal form - low-grade, seen in post distal femur w/ more mature ossification centrally |
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Hallmarks of HLA-B27 spondyloarthropathies
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bony ankylosis
proliferative new bone formation predom axial (spinal) syndesmophytes |
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arthritic involvement of SI joints
Differential and considerations |
- AS (bamboo spine, Andersen lesion and pseudoarthrosis),
- IBD (like AS) - psoriasis (distal jts, sausage digit, pencil-in-cup, acroosteolysis, proliferative erosions, STS, periostitis, ankylosis, arthritis mutilans deformities, heel spur w fuzzy margins - Reiter’s syndrome (like psoriasis but feet>hands, IP joint great toe), - DJD, gout - infection - HPT bilat + symmetric SIJ + marginal symmetric syndesmophytes – usually AS or IBD unilateral or asymmetric SI jt – NOT AS and IBD, consider psoriasis and Reiter’s |
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Large joint involvement in arthritis
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- DJD (superolateral migration in hips, medial compartment of knee most affected),
- RA (axial migration in hips), - CPPD - AS (resembles RA) - PVNS, synovial osteochondromatosis, - infection (S. aureus most comm, Salmonella in sicklers; + effusion, + joint destruction, crosses vert discs, periosteal rxn, bone destruction, Brodie’s abscess is well-defined lytic lesion with thick sclerotic border, sequestrum) - amyloidosis (nodular synovitis with erosions resembling RA) - ochronosis (DSN with vacuum, disc calcifications, generalized osteoporosis, secondary OA) |
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Arthropathy distribution in hands and wrists:
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Distal – OA, psoriasis, Reiter’s
Proximal – RA, CPPD Ulnar styloid - RA |
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Bilateral symmetry of arthropathy
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- Primary OA (middle-aged F in hands only, 1st CMC, gull-wing erosive pattern)
- RA - multicentric reticulohistiocytosis (mult erosions mostly phalanges NO osteoporosis) |
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Monoarticular arthritis
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CHRIST:
- Crystal arthropathies - Hemophilia - RA - Infection - Synovial (synovial osteochondromatosis, PVNS) - Trauma |
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Hallmarks of gout
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- erosions w/ sclerotic borders or overhanging edges
- soft tissue nod (can calcify w/ renal failure) - in hands –random dist, NO osteoporosis - podagra (1st MTP jt) - often have chondrocalcinosis - preserved joint space - olecr/prepatellar bursitis |
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Madelung’s deformity
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HITDOC:
- Hurler’s - Infection - Trauma - Dyschondrosteosis - Osteochondromatosis - Chromosomal anom (Turner’s) |
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Erlenmeyer flask deformity
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CHONG
- Craniometaphyseal dysplasia - Hemoglobinopathies ("hair on end" skull extramed. hematopoiesis) - Osteopetrosis - Neimann-Pick - Gaucher's |
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Arthritis with normal mineralization
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DJD
CPPD Gout multi. reticulohistiocytosis PVNS synovial osteochondromatosis |
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Epiphyseal enlargement and gracile diaphyses
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- hemophilia (hemarthrosis, 2˚ OA, wide intercond notch, big trochlear notch, subchondral cysts; pseudotumor – ST mass w/ adj bone destruction, hematoma, Ca++ common)
- JRA (diff ankylosis of post articular joints, periosteal new bone, STS, short metacarp) - paralysis |
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Causes of AVN
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ASEPTIC
-Anemia (SC), Amyloid -Steroids -Ethanol -Pancreatitis, Pregnancy -Trauma -Idiopathic (L-C-P) -Caisson dz, CVD |
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Tendon rupture
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steroids
RA DM HPT gout |
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Polydactyly
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familial
chondroectodermal dysplasia trisomy 13 Meckel-Gruber |
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Radial hypoplasia
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VACTERL
Holt-Oram syndrome Thrombocytopenia-absent radius syndrome |
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Distal tuft resorption
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PINCH FO
Psoriasis Injury (thermal) Neuropathy (DM, leprosy) CVD (Raynaud's, scleroderma) Hyperparathyroidism Familial (Hajdu-Cheney) Other - PVC tox |
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Periostitis without underlying bony lesion
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- Trauma
- HPO (pain, long bones; lung/ pleural CA, mets, chron PNA) - Venous stasis (legs) - Thyroid acropachy (post thyroidectomy, metacarpals & phalanges, esp ulnar aspect of 5th metacarpal) - Pachydermoperiostosis (like HPO but rarely painful) |
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Ivory vertebral body
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LIMP
– Lymphoma - Infection - Mets, myeloma - Paget’s |
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Ddx for diffuse dense bones
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Neoplasm
Mets, Myelofibrosis Mastocytosis, Lymphoma Congenital Craniotubular dysplasia Osteopetrosis Pyknodysostosis Sickle cell Metabolic Paget's Renal osteodystrophy Fluorosis Hypervitaminosis A&D |
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Periosteal reaction in children
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SCALP NIT
-Scurvy (dense metaph lines) -Caffey's (tib, ulna, mandib) -A hypervitaminosis -Lymphoma/leukemia -Physiologic, prostaglandins -Neuroblastoma -Infection -Trauma |
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Widened pubic symphysis
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bladder exstrophy
infection mets trauma pregnancy |
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Hallmarks of collagen vascular diseases
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osteoporosis and ST wasting in the hands, usually no erosions
SLE - ulnar deviation of phalanges, nonerosive, resembles Jaccoud’s arthropathy Scleroderma - ST Ca++, acroosteolysis, severe resorption of 1st CMC with radial subluxation of 1st metacarpal Dermatomyositis - widespread ST Ca++, radial subluxation of IP joint of thumb |
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CPPD-associated disorders
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primary HPT
gout hemochromatosis (DJD 2nd-4th MCP jts with squaring of metacarpal heads with drooping osteophytes, generalized osteoporosis) |
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Hallmarks of CPPD
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- pain
- cartilage Ca++ (knee, triangular fibrocartilage of wrist, pubic symphysis) - joint destruction from secondary DJD (shoulder, elbow, radiocarpal jt, patellofemoral jt) - subchondral cysts, can mimic gout |
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Lytic skull lesion
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SCD
HPT Paget’s FD TS infection mets, myeloma EG, epidermoid hemangioma |
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Lytic finger
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- Enchondroma
- Glomus tumor (pain, terminal phalanx) - Epidermoid inclusion cyst - Mets - Infection - Sarcoid - Erosive arthropathy |
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Dense metaphyseal lines
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- Growth recovery lines
- Lead - Healing rickets - Scurvy |
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Important features of
achondroplasia |
- shortened long bones w/ narrowing of interpedicular distance in caudal direction
- posterior vert body scalloping |
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Important features of melorrheostosis
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- thickened cortical new bone like “dripping candle wax”
- follows sclerotome |
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Important features of mucopolysaccharidoses
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- flattened vertebral bodies with anterior beak
- flared iliac wings and broad femoral necks - pointed proximal 5th metacarpal base w/notch look to ulnar aspect - posterior vertebral body scalloping |
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Important features of
multiple hereditary exostosis |
- osteochondromas
- metaphyseal - lesion grows away from joint, undertubulation, knees, proximal femur, axial more prone to degeneration |
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Important features of
osteoid osteoma |
- pain, age<30
- lucent nidus surr by reactive sclerosis in cortex of long bone - can be on concave side of painful scoliosis - “double density” sign on bone scan |
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Important features of
osteopathia striata |
- multiple 2-3mm thick linear bands of sclerotic bone aligned parallel to long axis of bone
- asymptomatic |
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Important features of
osteopoikilosis |
- asymptomatic
- mult small sclerotic densities @ ends of long bones & pelvis - hereditary |
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Important features of
acromegaly |
- skull thickening
- enlarged sinuses & sella - hypertrophied terminal tufts w/ spade appearance - posterior vertebral body scalloping - elongated & wide vert bodies - heel pad thickening |
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Important features of
transient osteoporosis of the hip |
- pain
- self-limited - low T1 signal - hot on bone scan |
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Features of intraosseous lipoma
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- asymptomatic
- proximal femur, fibula, calcaneus - may have central calcified nidus |
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Lytic lesion in sacrum
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- Mets
- Chordoma (sacral, clivus, vert body - expansile lytic lz w/ST component) - Plasmacytoma - Chondrosarcoma - GCT |
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Posterior vertebral scalloping
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- dural ectasia (NF, Marfan’s, Ehlers-Danlos)
- syrinx - spinal canal tumor - Congenital (achondroplasia, mucopolysacchar, OI) - Acromegaly |
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Protrusio acetabuli
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- RA
- Paget’s - AS - Trauma - IBD - Osteomalacia |
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Distal clavicle resorption
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RA
HPT osteomyelitis weightlifting trauma scleroderma |
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Platyspondyly
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Diffuse
----Dwarfism ----OI ----Morquio’s ----epiphyseal dysplasia ----Cushing’s Solitary or multifocal EG infection trauma mets, myeloma lymphoma, leukemia SCD osteonecrosis |
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Charcot joint
features |
6 Ds
Dense subchondral bone (sclerosis) Degeneration (attempted repair) Destruction (margins may appear surgical) Deformity Debris (loose bodies) Dislocation (nontraumatic) |
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Wormian Bones DDx
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-Pyknodysostosis
-Osteogenesis Imperfecta -Rickets in healing -Kinky Hair Syndrome -Cleidocranial Dysostosis -Hypothyroidism -Otopalatodigital syndrome -Pachydermoperiostosis -Primary Acro-osteolysis (Hajdu-Cheney) -Syndrome of Down -Idiopathic (can be normal, esp.<6 mo.) |
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DDx:
Arthritis Affecting the DIPs |
Psoriatic Arthritis
Osteoarthritis Erosive osteoarthritis Multicentr reticulohistiocytosis |
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Arthritis With Periostitis ddx
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Juvenile Rheumatoid Arthritis
Infectious arthritis Reiter’s syndrome Psoriatic Arthritis |
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Charcot joint causes
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DS6
Diabetes (insensitivity to pain) Syphilis (Tabes Dorsalis) Steroids Spinal cord injury Spina bifida Syringomyelia Scleroderma |
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DDx
Lytic Lesion Surrounded by Marked Sclerosis |
BOOST
Brodie’s Abscess Osteoblastoma Osteoid osteoma Stress fracture Tuberculosis |
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Causes of basilar invagination
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Paget’s disease
Fibrous Dysplasia Rickets OI, Osteomalacia Achondroplasia Cleidocranial dysplasia Hyperparathyroidism, Hurler’s |
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"Rugger Jersey” Spine
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"OH My"
Osteopetrosis Hyperparathyroidism Myelofibrosis |
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Vertebra Plana ddx
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Myeloma / Metastases
EG / Ewing’s Lymphoma / Leukemia Trauma (fx)/TB (infection) |
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Posterior vertebral body scalloping ddx
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NO MAAM
Neurofibromatosis (NF) Osteogenesis Imperfecta (OI) Marfan’s syndrome Achondroplasia (dwarf) Acromegaly Mucopolysaccharidosis |
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Osteoblastic metastases
|
"5B's Lick Pollen"
Bronchogenic (carcinoid) Bladder Breast Brain (medulloblastoma, GBM) Bowel (mucinous, carcinoid) Lymphoma Prostate Ca |
|
Dense base of skull DDx
|
-Fibrous dysplasia
-Engelmann’s (kids, cort thickening midshaft long bones inv periost & endost surf) -Von Buchem’s disease (adults) -Paget’s disease, -Pyknodysostosis -Meningioma -Osteopetrosis |
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Heel pad thickening
(> 25mm) DDx |
Myxedema,
Acromegaly Dilantin Callus Obesity Peripheral edema |
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Atlanto-axial subluxation
DDx |
RA
Trauma Downs' Morquio's |
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Short 4th metacarpal
DDx |
Idiopathic
PseudoHPT PseudopseudoHPT Turner's Basal cell nevus syndr (mandibular cysts, dural Ca++) |
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Widened teardrop in hip DDx
|
- Infection
- Trauma - PVNS (erosions, preserved jt space) - Synovial osteochondromatosis - AVN |
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MRI characteristics of PVNS
|
Villous or lobulated masses
T1 - INT to HI T2 - INT to HI Effusion Capsulosynovial thickening |
|
MRI characteristics of synovial chondromatosis
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Well defined rounded masses
T1 - LO T2 - LO Effusion Capsulosynovial thickening |
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MRI characteristics of lipoma arborescens
|
Villous or lobulated masses
T1 - HI T2 - LO Effusion Capsulosynovial thickening |
|
DDx
Skeletal MRI shows bright ring with dark center |
Common
- Osteoid osteoma - Bone infarct - Osteochonditis dissecans - AVN Uncommon - Brodie's abscess - EG - Melanoma mets |
|
Soft tissue mass on MRI
T2 bright with dark center |
Neurofibroma
Sarcoidosis Acute hematoma |
|
Soft tissue mass on MRI
moderate to marked T1 bright |
Lipoma
Hematoma Well-diff liposarcoma Myxoid liposarc or myxosarc |
|
Soft tissue mass on MRI
Homogeneously T1 dark |
Cyst
Ganglion Lymphocele Hygroma Seroma |
|
Soft tissue mass on MRI
mildly T1 bright rel. to muscle |
Neurilemmoma or neurofibroma
Hemangioma Abscess Solid malignancy (sarc or carci) Hemorrhagic mass |
|
DDx for lipohemarthrosis of the knee
|
* tibial plateau fracture
* ACL avulsion fracture * patellar dislocation w/ osteochondral injury |
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Arthritis affecting the DIPs
|
Psoriatic Arthritis
Osteoarthritis Erosive osteoarthritis Multicentric reticulohistiocytosis |
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Arthritis with Periostitis
|
Juvenile Rheumatoid Arthritis
Infectious arthritis Reiter’s syndrome Psoriatic Arthritis |