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47 Cards in this Set

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Bubbly or lytic lesions

FEGNOMASHIC - Fibrous Dysplasia, Enchondroma, Eosinophilic Granuloma, Giant Cell Tumor, Non-ossifying fibroma, osteoblastoma, Metastitc disease, Myeloma, Aneurysmal Bone Cyst, Solitary (unicamaral bone cyst), HPT, Infection, Chondroblastoma
fibrous dysplasia
no periosteal reaction, mention adamantinoma if in tibia or jaw; pelvis, proximal femur, ribs, skull, long lesion in long bone, expansile medullary lytic lesion, ground glass, well-defined sclerotic margin, bowing deformities, base of skull sclerotic, hot on bone scan, cherubism in mandible and maxilla, craniofacial in facial and frontal bones, pseudoarthrosis of tibia, Mccune Albright is polyostotic FD with café-au-lait spots with precocious puberty
enchondroma
must have calcifications except in phalanges, no periostitis; tubular bones, chondroid calcifications, endosteal scalloping, pain is malignant, Ollier’s enchondromatosis, Mafucci’s enchondromatosis with multiple ST hemangiomas
EG
age<30; lytic lesion can look aggressive, skull lesion beveled-edge appearance, sequestrum, floating tooth, vertebra plana, lung dz, pituitary, RES
GCT
epiphyses must be closed, must be epiphyseal and abut the articular surface in long bones, eccentric, well-defined but nonsclerotic border except in flat bones; long tubular bone > spine or sacrum, 50% at knee
NOF
age<30, no periostitis, cortically based; metaphysis
osteoblastoma
mention with ABC even if age>30, especially in posterior elements of spine
mets
age>40; renal and thyroid
myeloma
age>40; plasmacytoma in ilium and sacrum, cold on bone scan; vertebral bodies destroyed before pedicles, axial skeleton, long bones, punched-out lytic lesions, generalized osteopenia, skeletal survey more sensitive
ABC
age<30, expansile, eccentric, pain, fluid-fluid levels on MR; posterior elements of spine, metaphysis of long bones, pelvis
SBC (Unicamaral Bone Cyst)
age<30, central, no periostitis; proximal humerus, proximal femur, calcaneus, fallen fragment sign
Hyperparathyroidism
brown tumor, must have other evidence of HPT
infection
always mention
chondroblastoma
age<30, epiphyseal

chondromyxoid fibroma

mention with NOF, no calcified matrix

Mention in every case of bubbly or lytic lesions

Age<30 – infection, EG; age>40 – infection, mets, myeloma

Multiple Lytic Lesions

FEEMHI: fibrous dysplasia, enchondromas, EG, mets, myeloma, HPT, infection

Benign Appearing Rib Lesions

fibrous dysplasia, ABC, mets, myeloma, enchondroma, EG
Lytic epiphyseal lesion (also apophyseal, carpal and tarsal bones, patella)
chondroblastoma, infection, EG, GCT, geode; age>40 – add mets and myeloma and remove chondroblastoma
Lytic lesion in posterior elements of spine
OAT: osteoblastoma, ABC, TB
Exclude these lytic lesions if age>30
CANES: chondroblastoma, ABC, NOF, EG, SBC
Lesions that have no pain or periostitis
FENS: fibrous dysplasia, enchondroma, NOF, SBC
Bony sequestrum
FILE: fibrosarcoma, infection, lymphoma, EG, osteoid osteoma (mimic)

Geodes

CARD: CPPD, AVN, RA, DJD, trauma
Sclerotic lesion age 20-40
chondroblastoma, ABC, NOF, EG, SBC, fibrous dysplasia, infection, HPT (healing brown tumor), osteoid osteoma, giant bone island; age>40 – mets
Endosteal scalloping
ibrous dysplasia, enchondroma, cartilaginous tumor
Wide zone of transition (permeative)
mets + myeloma, reticulum cell sarcoma, Ewing’s sarcoma, infection, EG
Malignant bone tumors: age<30
Ewing Sarcoma, Osteosarcoma, Mets
Ewing’s sarcoma
diaphysis long bones > flat bones, aggressive, ST mass typical, medullary location
osteosarcoma
poorly defined intramedullary metaphyseal mass lesion extends through cortex, osteoid or chondroid matrix, aggressive periosteal reaction with Codman triangle or sunburst pattern
osteosarcoma telangiectatic form
purely lytic and simulates ABC, parosteal form is low-grade and seen in posterior distal femur with more mature ossification centrally
mets in children
neuroblastoma, leukemia/lymphoma, Wilm’s
Malignant bone tumors: age>40
mets + myeloma,chondrosarcoma

chondrosarcoma

pain, long bones, pelvis, ribs, clivus, most metaphyseal
Malignant bone tumors: age 30-40
GCT, Fibrosarcoma, Malignant Fibrous Histiocytoma, Reticulum Cell Sarcoma
GCT
if lung mets or recurrance
parosteal osteosarcoma
densest calcification is central
fibrosarcoma
almost always lytic
malignant fibrous histiocytoma
mention with fibrosarcoma, aggressive, large soft tissue mass
reticulum cell sarcoma
primary lymphoma of bone, looks like Ewing’s sarcoma, often asx
Permeative lesion in child
Ewing’s sarcoma, infection, EG
Permeative lesion in older pt
infection, mets, myeloma, malignant fibrous histiocytoma, reticulum cell sarcoma
Soft tissue tumors
MFH, liposarcoma (may or may not have fat), synovial sarcoma (usu extraarticular), synovial osteochondromatosis (multiple Ca++ loose bodies, jt effusion, erosions, destruction; knee, hip, elbow; mimics PVNS if not Ca++), pigmented villonodular synovitis (hemosiderin deposits lining synovium, erosions, jt destruction, no joint space narrowing), hemangiomas (phleboliths, cortical holes, striated vertebral body)
Malignant transformation of bony lesions
fibrous dysplasia – fibrosarcoma, OSA, MFH; Paget’s – OSA; osteomyelitis with draining sinus – SCC; radiation – OSA, chondrosarcoma, MFH; bone infarct – fibrosarcoma, MFH; Ollier’s – chondrosarcoma; Maffucci’s – chondrosarcoma; osteochondroma – chondrosarcoma
Cortical holes (pseudopermeative lesion)
osteoporosis (metacarpal cortex less then ¼ to 1/3 of metacarpal), radiation, hemangiomas
Focal cortical thickening
stress fracture, infection, osteoid osteoma

Mets to bone

PBKTL; P – mostly blastic, B – mixed, K – purely lytic, TL – mostly lytic