Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
57 Cards in this Set
- Front
- Back
What age group is particularly at risk?
|
Age <2O years old
|
|
ls an ABC generally painful?
|
Yes
|
|
What are the three most common anatomic locations?
|
Femur
Tibia Posterior spine |
|
Are ABCs usually located centrally within bone?
|
No; eccentric
|
|
Are ABCs usually lytic or blastic?
|
Lytic with thin periosteal rim
|
|
Where might an ABC extend into?
|
Adjacent soft tissue
|
|
What is the classic MRI feature of an ABC?
|
Fluid-fluid levels
|
|
What are the histologic features?
|
Cavernous spaces without endothelial lining
|
|
What has a similar histology? Key difference?
|
Hemangioma (similar histology with epithelial lining)
|
|
lf a very cellular stroma is present, what diagnosis must be considered?
|
Telangiectatic osteosarcoma
|
|
What is the usual treatment for an ABC?
|
Curettage and bone graft
|
|
ABCs are most likely to recur in what patients?
|
Those with open physes
|
|
What two anatomic locations are most commonly affected?
|
Proximal humerus
Proximal femur |
|
ln what two places are unicameral bone cysts (UBCs) generally found within bone?
|
Central (compare with ABC: eccentric)
Metaphyseal (compare with giant cell tumor [GCT]: epiphyseal) |
|
What are the two histologic features?
|
Clear, fluid-filled cyst lined by thin membrane of fibrous tissue
May see some multinucleated giant cells |
|
What are the two components of first-line treatment?
|
Aspiration
Steroid injection |
|
What is the treatment of a recurrent lesion or an impending fracture?
|
Curettage and bone graft
|
|
ln lower extremities, consider what treatment for impending pathologic fracture?
|
ORIF
|
|
Is EG benign or maligant?
|
Benign
|
|
What are the two plain radiographic features?
|
Destructive (lytic) lesion with distinct margins
Generally, no associated soft tissue mass |
|
How does an involved vertebral body classically appear?
|
Vertebra plana (uniformly collapsed)
|
|
What are the four key histologic features?
|
Eosinophils
Cigar-shaped nuclei Pale histiocytes Birbeck granules (racquet-shaped inclusion bodies in cytoplasm on electron microscopy) |
|
Is histiocytosis generally a self-limited condition?
|
Yes
|
|
What are two local treatment options?
|
Observation
Curettage and bone graft |
|
What are the different types of EG?
|
Single-bone disease (most common,approximately 80%)
Multiple-bone disease Bone disease with systemic and visceral involvement |
|
What are two systemic diseases?
|
Hand-SchUller-Christian disease
Letterer-Siwe disease |
|
What are the three features of Hand-Schuller-Christian syndrome?
|
Exophthalmos
Diabetes insipidus Lytic skull lesions |
|
What age group is affected by Letterer-Siwe disease?
|
Children <3 years old
|
|
What are the four features of Letterer-Siwe?
|
Multiple bony lesions
Anemia Bacterial infections Hepatosplenomegaly |
|
What is the prognosis?
|
Fatal
|
|
ls giant cell tumor benign or malignant?
|
Benign but can be locally aggressive
|
|
What gender is more commonly affected?
|
Female (1.5:1)
|
|
What are the three most common anatomic locations involved?
|
Knee
Spine/sacrum Distal radius |
|
What is the typical location within bone?
|
Epiphysis
|
|
Are physes generally open or closed?
|
Physes are generally closed
|
|
Contrast with physeal status in what other disorder?
|
Chondroblastoma: physes are generally open
|
|
Giant cell tumors may degenerate into what lesions?
|
Aneurysmal bone cyst
Other neoplasms |
|
What is the appearance of giant cell tumor on bone scan?
|
Doughnut: intense circumference,central lytic area
|
|
ln what two ways are giant cell tumors treated?
|
Curettage and bone grafting or polymethylmethacrylate (PMMA) with adjuvant (eg., phenol, cautery): 25% recur Marginal resection if multiply
recurrent or extensive bony destruction |
|
What is the likelihood of developing metastases?
|
3% incidence of benign pulmonary metastases
|
|
What two anatomic locations are most commonly involved?
|
Hands/feet
Jaw |
|
What is the typical radiographic appearance?
|
Lytic, eccentric
|
|
Histologically, giant cell reparative granuloma may resemble what? There a difference?
|
Giant cell tumor
Bone is present |
|
What population is most commonly affected by myositis ossificans (MO)?
|
Athletes
|
|
Where is the ossihcation generally seen radiographically?
|
The ossification is generally periosteally based
|
|
What are the histologic features of the periphery and the center?
|
Periphery: mature (eggshell)
Center: immature |
|
How is MO treated?
|
Initial immobilization as Nonsteroidal antiinflammatoiy drugs ,
(NSAIDs) |
|
How and when should mobilization be resumed?
|
Begin active range of motion after 2 days
Avoid passive stretching |
|
What is MO progressiva?
|
Autosomal dominant disorder with multiple sites of ossitication
|
|
What is the etiology of these lesions?
|
Posttraumatic
Arise from subperiosteal hemorrhage |
|
What diagnosis comes to mind if the lesion resembles callus?
|
Florid reactive periostitis
|
|
What diagnosis comes to mind if the lesion resembles osteochondroma with cartilage cap?
|
Bizarre parosteal osteochondromatous proliferation (BPOP)
|
|
What diagnosis comes to mind if the lesion is found under the nail?
|
Subungual exostosis
|
|
What patient population is particularly at risk?
|
African descent
|
|
What are the most common anatomic locations of tumoral calcinosis?
|
Extensor surfaces
|
|
In affected patients, what is the usual serum calcium concentration?
|
Normal
|
|
What is the histologic appearance?
|
Hydroxyapatite crystals
|