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37 Cards in this Set

  • Front
  • Back
MR characteristics of chondroblastoma
lobulated cartilage appearance with substantial edema
only cartilage lesion that is low/intermediate T2
extensive surrounding edema
+/- joint efusion
+/- periosteal rxn
lesion that simulates a chondroblastoma but is seen in older pts
typical location and appearance of this lesion
clear cell chondrosarcoma
epiphysis
different from chondroblastoma b/c is bright on t2
imaging characteristics that to distinguish giant cell tumor from chondroblastoma
gct rare in teenagers (need closed epiphysis)
no bone marrow edema or periosteal rxn
low T2
management of gct
curettage and methylmetacrylate
t or f: giant cell tumors can metastasize
true!
early appearance of primary bone leukemia
focal nodular replacement of bone marrow
intense enhnaceemnt
no loss of signal on out of phase imaging
appearance of a morton neuroma
between metatarsal heads and neck
dumbbell shaped mass with intermediate to low t1 and t2
will see replacement of nml fat on T1 short axis
+enhancement
what is dx if you are in 2nd interspace and there are both high and low signal within a dumbbell shaped lesion on T2
morton's neuroma + bursitis
what is a morton's neuroma
fibrosing process from compression of the plantar digital nerve
how to differentiate between hibernoma and lipoma
hibernomas don't exhibit rapid growth
hibernoma: dirty fat, high on T2, t1 variable, but usually darker than subQ fat
low signal septations are common
appearance of chordoma
usually in sacrum
locally destructive, lytic lesion
can get very large
high on t2, low /iso t1
may have calcs peripherally
typical appearance of telangiectatic osteosarcoma
lytic and expansile
fluid levels common
areas of cortical disruption
can be misdx as an abc
when should the possiblity of angiosarcoma be suggested
multiple lytic lesions clustered in a single anatomic region
thing to suggest benign vs malignant osteochondroma
look at the cartilage cap, if greater than 2cm, suggests malig (although not a hard and fast rule, esp in a pt who is growing)
at what age does malig transformation of osteochondroma usually occur
25-30 yo
loc of enchondroma
central, often metaphyseal
appearance of enchondroma in short tubular bones
expansile remodeling with prominent thinned cortex (in short tubular bones)
why do enchondromas have a lobulated appearance on mr
all hyaline cartilage lesions grow in lobules.
bones get scalloped, but unevenly
why is there ring and arc appearance on xr in bone infarcts
it's artifactual (just due to serpiginus margins of bone infarct seen en face)
there is no true ring and arc mineralization in bone infarct
aids to differentiate enchondroma vs chondrosarcoma
enchondroma: rare in axial ske, common in hand/foot, common in long bones, painless, endosteal scalloping <2/3 cortex, no cortical thickening or periosteal rxn;

chondrosarc:common in axial skeleton, long bones, rare in hand/foot; pain, endosteal scalloping depth >2/3 cortex, +/- cortical thickening and periosteal rxn, enhancement

change over time would favor chondrosarc
most frequently seen aggressive lytic primary tumors in 30-60 yo
fibrosarcoma
mfh
histioctyoma of bone
primary lymphoma of bone
appearance of sarcoid in teh bone
lace-like lytic lesions in the hands and feet
mr appearance of sarcoid of the bone
low t1, high t2
+enhancement
most common in the metaphyses
osseous abnormalities assoc with ts
hyperostosis of inner table +sclerotic foci
hypertrophic osteoarthropathy in hands and feet
what is the most common phalangeal tumor
enchondroma
what lesion to think of when you see columns of cartilage extending into metaphysis from epiphyseal plate
enchondroma (or other cartilagenous lesion)
t or f: cupping can be seen in the physis adjacent to enchondromas in ollier's disease
true
t or f: ollier's disease is most often b/l
false, usually unilateral
complications of ollier disease
chondrosarcoma
mode of inheritance in ollier disease
not hereditary
complications/other diseases assoc with maffucci syndrome
chondrosarc
vascular sarcoma
ovarian, pancreatic malign
gliom/carcinoid
findings of metaphyseal dysplasia
flaring of the ends of long bones with constriction and sclerosis of diaphysis
mild cranial sclerosis
can cause erlenmeyer flask deformity
another name for metaphyseal dysplasia
pyle's disease
which type of chondrosarcoma can have a rim of sclerosis
clear cell chondrosarcoma, similuate a non-aggressive lesion
how to differentiate chondroblastoma from clear cell chondrosarcoma
both are epiphyseal lesions
older age in clear cell chondrosarc
no surrounding BM edema (which there is a lot of in chondroblastoma)
imaging features of an atypical llipomatous tumor
thickend enhancing septum and nodules
what is atypical lipomatous tumor indistinguishable from
well defferentiated liposarcoma