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147 Cards in this Set
- Front
- Back
benign bone tumor which settles with aspirin at night |
osteoid osteoma |
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Are osteoid osteomas typically large lesions? |
N. |
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osteoid osteoma
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osteoid osteoma |
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osteoid osteoma |
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FEGNOMASHIC:F =E = G =
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fibrous dysplasia,enchondroma / eosinophilic granuloma,giant cell tumour
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FEGNOMASHIC: NO
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nonossifying fibroma, osteoid osteoma
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FEGNOMASHIC: M= A= S= |
metastasis/myeloma, aneurysmal bone cyst, solitary bone cyst.
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FEGNOMASHIC: H= , I= , C= .
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hyperparathyroidism, infection, chondroblastoma. |
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When determining differential diagnosis for bone tumors, what are the first things you ask yourself? |
1. morphology 2. age
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what 4 arthropathies are associated with subchondral geodes?
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RA, DJD, CPPD, AN.
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osteoid osteoma tends to arise in which age group? {__-__} years.
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10-20
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where is osteoid osteoma most commonly found? {proximal/distal cortex/medulla of ____ or _____}
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proximal cortex of femur or tibia |
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describe the typical appearance of osteoid osteoma {focal area of ___ ____ with a central _____ _____}
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focal area of cortical thickening with a central radiolucent nidus.
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Fibrous displasia looks like
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can look like almost anything.
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What syndrome is fibrous dysplasia associated with? (other than Mazabraud syndrome)
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McCune-Albright Syndrome
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What is the classic triad defining McCune Albright syndrome
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polyostotic fibrous dysplasia, endocrine dysfunction, cutaneous hyperpingmentation.
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the other name for cutaneous hyperpigmentation
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cafe au lait spots
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What is the typical symptom of endocrine dysfunction in Maccune Allbright syndrome?
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precocious puberty.
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The most common cystic lesion of the phalanges
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enchondroma
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this is a
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osteochondroma
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It is difficult to differentiate between an enchondroma and a {___ ____}
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Bone infarct
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enchondroma
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well defined, densely sclerotic serpinginous boarder without scalloping is a characteristic of a {_}, not a {_}
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bone infarct, enchondroma
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What differentiates an enchondroma from a chondrosarcoma? |
pain
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Is histology useful for differentiating chondrosarcoma from enchondroma? What could be reassuring? {_}. {_}.
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no. MRI.
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Multiple enchondromas is called {_________'s} disease.
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Ollier's
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What four bony lesions occasionally have bone sequestra?
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Osteomylitis, lymphoma, fibrosarcoma, eosinophilic granuloma.
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What is the typical age of a patient with eosinophlic granuloma? { __.}
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< 30.
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To where do giant cell tumors rarely metastasize? {_.}
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lung.
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Where do giant cell tumours occur?
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epyphysis |
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Are giant cell tumors usually large or small?
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large. |
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for GCT: the zone of transition is {_}, T/F - the boarder is sclerotic {_}
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narrow. F.
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What is the most common benign bone lesion encountered by radiologists?
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Nonossifying fibroma |
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What is the typical age of a patient with a nonossifying fibroma? {_} and what is the penetrance? {__%}
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young. 20%. |
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Do nonossifying fibromas typically involve the cortex?
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Y
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Describe the boarder of a nonossifynig fibroma
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sclerotic, thin.
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Is periostitis associated with a non-ossifying fibroma and is the lesion painful? {_, _.}
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N, N.
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Is osteoblastoma a common lesion?
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N.
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Diffuse calvarial hyperostosis can be caused by which drug?
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phenytoin
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What are the 4 subtypes of fibrous dysplasia
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monostotic polyostotic craniofacial fibrous dysplasia cherubism (mandible and maxilla affected only)
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Malignant differential of fibrous dysplasia in the tibia or mandible
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adamantinoma
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What is a langerhans cell?
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antigen presenting cell (dendritic cell) found in the skin and mucosa.
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what differentiates a Langerhans cell from a histiocyte?
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Birbeck granules. (looks like a tennis raquet).
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unifocal langerhans cell histiocytosis is also known as?
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eosinophilic granuloma
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What is the Hand-Schuller-Christian triad?
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diabetes insipidus, exopthalmos, lytic bone lesions
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What is Letterer-Siwe disease? {multi/uni focus, system, _ _}
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multifocal, multisystem Langerhans histiocytosis.
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What is pulmonary langerhans cell histiocytosis?
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A not-completely seperate disorder almost always (95%) seen in adult smokers (20-40 years old) and sometimes resulting in progressive pulmonary fibrosis.
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How do you differentiate benign or malignant GCT?
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recurrence.
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How many appearances does eosinophilic granuloma have and is it associated with pain?
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many, sometimes
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what is one useful descriminator and two less useful descriminator for EG? {__, __stotic. _ _}
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age, monostotic. Bony sequestrum.
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What is the other common presentation of enchomdroma ?
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Irregular speckled calcification in the distal femur.
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What is the age prediliction of enchondroma? {_ age, but usually _}
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Any age, but usually adults.
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What is "benign fibrous cortical defect synonomous with?.
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non-ossifying fibroma
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DDx for a lesion with no periostitis or pain
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fibrous dysplasia enchondroma NOF SBCEG (sometimes has pain)
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DDx for an epiphyseal lesion
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geodeinfectionchondroblastoma GCT
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DDx for multiple bone lesions
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fibrous dysplasia EG enchondroma mets / myeloma HPT infection
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In what location are solitary bone cysts found?
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Invariably central, never epiphysial, often proximal humerus or proximal femur.
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What is the age prediliction for SBC?
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< 30.
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What featre of HPT must be seen to diagnose a brown tumour?
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subperiostial resorbtion: phalanges, distal clavicles, medial aspect of proximal tibias. Looser's zone fractures.
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An aneurysmal bone cyst is virtually always . . . {_ or _}
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aneurysmal or expansile
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What is the characteristic appearance of an ABC on MRI?
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multiple cavities with fluid levels. (almost pathognomonic)
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What is the age prediliection for an ABC?
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less than 30 years old.
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Are ABC's associated with pain?
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yes.
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What is a typical location of an ABC and where can they occur?
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Typically posterior elements of the spine, but can occur anywhere.
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What are ABC discriminators?
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must be expansile patients must be younger than 30 years of age.
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does a non-ossifying fibroma involve the cortex?
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yes, it will replace it with fibrous tissue.
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where do non-ossifying fibroma's occur?
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usually around the knee but can occur in any long bone.
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What is the DDx of a lytic bone lesion in the epiphysis of a young patient (< 30 years)
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infection (most common) chondroblastoma GCT rare - ABC and EG
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what diseases are associated with subchondral cysts (geodes)
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degenerative joint disease (must be associated with joint space narrowing, subchondral sclerosis and osteophyte formation) rheumatoid arthritis calcium pyrophosphate dihydrate deposition disease (CPPDDD) avascular necrosis
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Chondrobastoma discriminators
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patient must be younger than 30 years must be epiphyseal.
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What can never be excluded in a patient younger than 30 years?
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Eosinophilic granuloma infection
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What can never be excluded in a patient over 40 years old?
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metastatic disease infection
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What are 4 useful radiologic criteria for determining whether a lesion is malignant or benign?
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cortical destruction - not really periostitis - difficult to differentiate "aggressive" from "benign" orientation of the lesion - not helpful at all zone of transition - yes!
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osteoid osteoma
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osteoid osteoma |
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Salient features of osteoid osteoma |
* nidus (meshwork of dilated vessels and osteoclasts) * fibrovascular rim * surrounding reactive sclerosis |
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Can a non-ossifying fibroma involve the cortex
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yes, the cortex may be replaced by benign fibrous tissue. |
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fibrous dysplasia |
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fibrous dysplasia - polystotic form |
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Fibrous dysplasia - monostotic |
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Giant Cell Tumour |
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Giant cell tumour |
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non-ossifying fibroma
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Giant cell tumour of bone |
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Aneurysmal bone cyst |
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healing non-ossifying fibroma |
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Other name for a solitary bone cyst
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unicameral bone cyst
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simple bone cyst (unicameral)
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T2 weighted. Lesion returns low signal on T1. |
unicameral (simple) bone cyst
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unicameral (simple) bone cyst
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T2 image. T1 signal was low also
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non-ossifying fibroma |
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What are the MRI appearances of non-ossifying fibroma? |
T1 low signalT2 variable. intermediate to high initially, then low as the lesion ossifys.
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osteochondroma
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Frontal view of the left shoulder shows expansion of the proximal left humeral diametaphysis with a ground glass matrix and adjacent cortical thinning. There is a left proximal humeral bony excrescence as well as a protrusion of the cortex medially. In addition, there is a bony protuberance projecting from the medial mid left scapula. These findings are suggestive of Hereditary multiple exostoses (HME), which is characterized by the presence of multiple osteochondromas. |
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define excrescence |
abnormal outgrowth |
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identify this lesion |
enchondroma
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p |
enchondroma |
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p |
enchondroma |
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T1, lesion high signal on T2. Note surrouding |
enchondroma
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renal cell carcinoma
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chondroblastoma
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What is the tissue of origin for chondroblastoma |
-Usually benign, cartilaginous tumor |
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What is the key radiologic feature? |
-Epiphyseal lytic lesion in children and teens
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is a chondrobastoma usually painful? |
Yes. |
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osteoid osteoma epidemiology (__ to __ years, M:F) |
10 to 25 years, 3:1
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enchondroma is a |
benign tumour of hyaline cartilage
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what gives an enchondroma its characteristic "speckled appearance" |
chondroid matrix |
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What disease and what syndrome are multiple enchondromas (and hemangiomas) associated with?
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Ollier disease, Maffuci syndrome
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"automatics" where patient is younger than 30 years old? |
eosinophilic granuloma infection |
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"automatics" if patient is more than 30 years old |
metastasis infection |
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Discriminator for fibrous dysplasia
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No periosteal reaction |
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If fibrous dysplasia is suspected in the tibia ___ should also be considered
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adamantinoma
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Enchondroma descriminators
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Calcification, no pain
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Eosinophilic granuloma discriminators
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younger than 30.
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Giant cell tumour descriminators
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epiphyses closed, abuts articular surface, well defined with non-sclerotic margin.
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Non ossifying fibroma descriminators
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younger than 30, no periostitis.
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Aneurysmal bone cyst descriminators
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expansile, younger than 30.
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Solitary bone cyst
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central, younger than 30. |
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Chondroblastoma descriminators
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epiphyseal, younger than 30.
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4 criteria useful for determining malignant nersus benign lesions:
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cortical destruction, periostitis, axis, zone of transition.
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most important descriminator of bone malignancy
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zone of transition
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mallignant tumours will appear to have a ___ zone of transition on MRI
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narrow
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benign periostitis appears as
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cortical thickening |
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malignant periostitis characterised by {sun___, amo___, co___ ____, o___ s___}
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sunburst, amorphous, codman triangle, onion skin. |
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The only two childhood malignant tumour of bone
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osteosarcoma, Ewings sarcoma |
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Common malignant tumours of bone in adulthood
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metastasis, myeloma, chondrosarcoma.
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most common malignant bone tumour
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osteosarcoma |
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In what circumstances might osteosarcoma be found in an older person?
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padget's disease, radiation induced
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T/F: parosteal osteosarcoma is more aggressive.
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F
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cortical desmoid occures at the insertion / origin of { __ __ of __ or __ __}
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medial head of gastrocnemius or adductor magnus
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benign avulsion injury of distal femur |
cortical desmoid
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p |
myositis ossificans |
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3 "knee jerk" diagnoses for a permeative lesion in a child:
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Ewing sarcoma, infection, eosinophilic granuloma.
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Is Ewings sarcoma usually symptomatic
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Y |
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Low grade chondrosarcoma appears very similar histiologically to:
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enchondroma |
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Differentials for lytic lesion with aggressive features in an older patient
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metastasis, plasmacytoma, fibrosarcoma, malignant fibrous histiocytoma, infection. |
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What are the two most common soft tissue tumours?
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MFH and liposarcoma
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Osteochondroma
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Cartilage-capped osseous excrescence with continuous cortex and marrow extending from underlying bone.
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Chondroblastoma
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Benign cartilage tumor arising in epiphysis of skeletally immature individuals
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parosteal
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pertaining to the outer surface of the periosteum
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Leterer-Siwe Disease
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Multifocal, multiorgan LCH. |
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3 Types of Langerhans cell histiocytosis
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1) Leterer-Siwe Disease 2) Uni/multifocal Unisystem. 3) Pulmonary LCH |
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melorheostosis
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flowing segmental ossification (dripping candle wax sign) |
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periosteal chondroma (juxtacortical chondroma) |
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What angle is this? |
Bohler angle |
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9 year old boy |
Askin tumour |